Treatment of Breast Cancer-related Lymphedema With a Negative Pressure Device

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT03252145
Collaborator
Foundation for Physical Therapy, Inc. (Industry)
28
1
2
27
1

Study Details

Study Description

Brief Summary

This study will be a 4 to 6 week randomized, controlled, assessor blinded, trial comparing a negative pressure massage device (intervention group), to the standard manual lymph drainage massage (control group), in breast cancer patients with chronic upper extremity lymphedema.

Condition or Disease Intervention/Treatment Phase
  • Device: PhysioTouch
  • Other: Manual Lymph Drainage (MLD)
N/A

Detailed Description

Lymphedema (LE) is a protein-rich interstitial swelling caused by reduced lymph transport secondary to lymphatic system damage from cancer treatments. 1 in 5 women will develop LE following breast cancer treatment. These women have greater restrictions in activity and poorer quality of life (QOL) and are more prone to cellulitis than women without LE. LE is incurable and progressive. Persistent lymph stasis creates a condition of chronic inflammation that contributes to fibrosis and fatty deposition in the subcutis of the affected limb. The fibro-adipose changes associated with chronic LE make it less responsive to treatments that primarily target limb volume. Treatments are needed that can improve these skin and subcutaneous tissues changes, as well as reduce limb volume.

This 4 to 6 week randomized controlled pilot feasibility study will enroll 80 women with chronic arm LE, and will evaluate a novel negative pressure massage device that mobilizes skin and subcutaneous tissue. This negative pressure treatment provides vertical (lifting) and horizontal stretching of the skin and underlying fascial structures, which increases the subcutaneous space for lymphatic circulation, improves lymph flow, and has the potential to decrease fibrosis. This treatment will be compared to the standard of care massage: manual lymphatic drainage. Women will be randomly assigned to either the negative pressure massage device (intervention group), to the standard manual lymph drainage massage (control group)

Objectives: To evaluate recruitment and retention rates; to determine rates of adverse events; and to determine effect sizes for limb volume, tissue induration; and patient reported outcomes of arm function, QOL, and body image in response to treatment

Study Design

Study Type:
Interventional
Actual Enrollment :
28 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Treatment of Breast Cancer-related Lymphedema With a Negative Pressure Device: A Feasibility Study
Actual Study Start Date :
Oct 31, 2017
Actual Primary Completion Date :
Jan 31, 2020
Actual Study Completion Date :
Jan 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Negative Pressure

PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb

Device: PhysioTouch
The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.

Active Comparator: Manual Lymph Drainage

Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb

Other: Manual Lymph Drainage (MLD)
MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid.

Outcome Measures

Primary Outcome Measures

  1. Recruitment Rates [At 4 weeks]

    The recruitment rate is defined as the number of women who were screened and then enrolled on the study divided by the the total number of women screened overall.

  2. Percentage of Participants Who Completed All Study Visits [At 4 weeks]

    Retention rates for both arms of this study were evaluated. The numbers of women who completed the study will be recorded. Reasons for drop out will be ascertained.

Secondary Outcome Measures

  1. Mean Limb Volume [At Baseline]

    Arm circumferential measurements of both limbs and hands were taken twice, using a spring-loaded tape measure. The hand was measured in two locations. Upper extremity measurements were taken at 10 centimeter (cm) intervals from the ulnar styloid of the wrist up to a total distance of 40 cm. Circumferences were measured using the procedures outlined by Cornish et al. Limb volume was calculated using the formula for volume of a truncated cone and reported in millilitre (ml)

  2. Mean Limb Volume [At 4 weeks]

    Arm circumferential measurements of both limbs and hands were taken twice, using a spring-loaded tape measure. The hand was measured in two locations. Upper extremity measurements were taken at 10 centimeter (cm) intervals from the ulnar styloid of the wrist up to a total distance of 40 cm. Circumferences were measured using the procedures outlined by Cornish et al. Limb volume was calculated using the formula for volume of a truncated cone and reported in millilitre (ml)

  3. Mean Lymphedema Index (L-DEX®) Ratio Scores [At Baseline]

    Bioimpedance spectroscopy (BIS) measurements were taken using a single channel BIS, tetrapolar device (LDex device, ImpediMed, San Diego, CA) to evaluate upper limb bioelectrical impedance. Impedance ratios (unaffected/affected limb) are calculated and converted to L-Dex ratio score. With development of lymphedema, impedance of extremity decreases and L-Dex ratio therefore increases. An L-Dex ratio score of 10 is equivalent to impedance ratio of 1.139 (which is = to 3 standard deviations (SD) from mean normative BIS data) for at-risk dominant arms & 1.066 for at-risk non-dominant arms, respectively. Each 1 standard unit in L-Dex is equivalent to impedance ratio of 0.03. Using this arbitrary scale relevant to normative standards, a patient is determined to have arm lymphedema if L-Dex ratio score exceeds 7.1, which is 2 SD above mean normative data for BIS impedance ratios. Higher L-Dex ratio score means higher impedance ratio between limbs, which means more volume in affected limb.

  4. Mean L-DEX® Scores [At 4 weeks]

    Bioimpedance spectroscopy (BIS) measurements were taken using a single channel BIS, tetrapolar device (LDex device, ImpediMed, San Diego, CA) to evaluate upper limb bioelectrical impedance. Impedance ratios (unaffected/affected limb) are calculated and converted to L-Dex ratio score. With development of lymphedema, impedance of extremity decreases and L-Dex ratio therefore increases. An L-Dex ratio score of 10 is equivalent to impedance ratio of 1.139 (which is = to 3 standard deviations (SD) from mean normative BIS data) for at-risk dominant arms & 1.066 for at-risk non-dominant arms, respectively. Each 1 standard unit in L-Dex is equivalent to impedance ratio of 0.03. Using this arbitrary scale relevant to normative standards, a patient is determined to have arm lymphedema if L-Dex ratio score exceeds 7.1, which is 2 SD above mean normative data for BIS impedance ratios. Higher L-Dex ratio score means higher impedance ratio between limbs, which means more volume in affected limb.

  5. Mean Skin Induration Score [At Baseline]

    The SkinFibroMeter (Delfin Technologies, Finland) was used to measure tissue induration. The SkinFibroMeter consists of a 1 mm long indenter and a force sensor. The device is gently pressed against the skin. The indenter imposes a constant deformation when the reference plate is in full contact with the skin. The skin and the underlying superficial subcutis resist the deformation. Measurements will be taken bilaterally at 5 locations: the first dorsal web space; the medial forearm halfway between the ulnar styloid and medial epicondyle; the lateral forearm halfway between the radial styloid and the lateral epicondyle; the medial arm 3 inches proximal to the medial epicondyle; and the lateral arm 3 inches proximal to the lateral epicondyle. Five recordings were taken at each location and a mean score was calculated.The induration value in Newtons (N) is recorded.

  6. Mean Skin Induration Score [At 4 weeks]

    The SkinFibroMeter (Delfin Technologies, Finland) was used to measure tissue induration. The SkinFibroMeter consists of a 1 mm long indenter and a force sensor. The device is gently pressed against the skin. The indenter imposes a constant deformation when the reference plate is in full contact with the skin. The skin and the underlying superficial subcutis resist the deformation. Measurements will be taken bilaterally at 5 locations: the first dorsal web space; the medial forearm halfway between the ulnar styloid and medial epicondyle; the lateral forearm halfway between the radial styloid and the lateral epicondyle; the medial arm 3 inches proximal to the medial epicondyle; and the lateral arm 3 inches proximal to the lateral epicondyle. Five recordings were taken at each location and a mean score was calculated.The induration value in Newtons (N) is recorded.

  7. Mean Degrees of Shoulder Range of Motion [At Baseline]

    Active shoulder flexion and abduction range of motion (ROM) was assessed, with patients supine, using a goniometer and standardized procedures reported by Norkin and White. Bilateral ROM was assessed. Two measurements will be taken for each motion and a mean obtained, for each, bilaterally. Findings are recorded in degrees.

  8. Mean Degrees of Shoulder Range of Motion [At 4 weeks]

    Active shoulder flexion and abduction range of motion (ROM) was assessed, with patients supine, using a goniometer and standardized procedures reported by Norkin and White. Bilateral ROM was assessed. Two measurements will be taken for each motion and a mean obtained, for each, bilaterally. Findings are recorded in degrees.

  9. Mean Grip Score [At Baseline]

    Grip strength was assessed using a Jamar hydraulic hand dynamometer (Patterson Medical, Bolingbrook, IL). Patients will be tested in sitting with the feet flat on the floor, the arm at the side with the elbow flexed to 90 degrees. The patient was instructed to maximally squeeze the handle and hold for a count of 3. The peak-hold needle will automatically record the highest force exerted. Two trials for each extremity will be done and a mean grip score (in kilogram of force) calculated. A higher score indicates a greater grip strength.

  10. Mean Grip Score [At 4 weeks]

    Grip strength was assessed using a Jamar hydraulic hand dynamometer (Patterson Medical, Bolingbrook, IL). Patients will be tested in sitting with the feet flat on the floor, the arm at the side with the elbow flexed to 90 degrees. The patient was instructed to maximally squeeze the handle and hold for a count of 3. The peak-hold needle will automatically record the highest force exerted. Two trials for each extremity will be done and a mean grip score (in kilograms of force) calculated. A higher score indicates a greater grip strength.

  11. Mean Karnofsky Performance Status (KPS) Score [At Baseline]

    Participants rated their functional status using the single item KPS scale with a range from 0 (dead) to 100 (I feel normal; I have no complaints or symptoms), in increments of 10 (0,10,20, 30 , 40...). The lower the Karnofsky score, the worse the impairment.

  12. Mean Karnofsky Performance Status (KPS) Score [At 4 weeks]

    Participants rated their functional status using the single item KPS scale with a range from 0 (dead) to 100 (I feel normal; I have no complaints or symptoms), in increments of 10 (0,10,20, 30 , 40...). The lower the Karnofsky score, the worse the impairment.

  13. Mean Self-Administered Comorbidity Questionnaire (SCQ) Scores [At Baseline]

    The SCQ consists of 13 common medical conditions that are simplified into language that could be understood without any prior medical knowledge. Patients were asked to indicate if they had the condition using a "yes/no" format. If they indicate that they had a condition, they are asked if they received treatment for it (yes/no; proxy for disease severity) and did it limit their activities (yes/no; indication of functional limitations). • For each condition, a patient can receive a maximum of 3 points. Because there are 13 defined medical conditions and 2 optional conditions, the maximum achievable total score is 45 points as all items were available for use.

  14. Mean Self-Administered Comorbidity Questionnaire (SCQ) Scores [4 weeks]

    The SCQ consists of 13 common medical conditions that are simplified into language that could be understood without any prior medical knowledge. Patients were asked to indicate if they had the condition using a "yes/no" format. If they indicate that they had a condition, they are asked if they received treatment for it (yes/no; proxy for disease severity) and did it limit their activities (yes/no; indication of functional limitations). • For each condition, a patient can receive a maximum of 3 points. Because there are 13 defined medical conditions and 2 optional conditions, the maximum achievable total score is 45 points as all items were available for use.

  15. Mean Norman Questionnaire (NQ) Scores [At Baseline]

    The NQ was originally developed and validated as a phone interview questionnaire to describe the signs and symptoms of breast cancer-related lymphoedema. Participants report subjective differences in the size of the hands, lower arms, and/or upper arms between their right and left sides. For each site difference, the reported score can range from 1 (very slight difference) to 3 (very noticeable difference). The total score can range from 1 (very slight difference at 1 site) to 9 (very noticeable difference at all 3 sites). Higher scores indicate a greater noticeable difference between the two arms

  16. Mean Norman Questionnaire (NQ) Scores [At 4 weeks]

    The NQ was originally developed and validated as a phone interview questionnaire to describe the signs and symptoms of breast cancer-related lymphoedema. Participants report subjective differences in the size of the hands, lower arms, and/or upper arms between their right and left sides. For each site difference, the reported score can range from 1 (very slight difference) to 3 (very noticeable difference). The total score can range from 1 (very slight difference at 1 site) to 9 (very noticeable difference at all 3 sites). Higher scores indicate a greater noticeable difference between the two arms

  17. Mean Norman Questionnaire (NQ) Scores [At 4 months]

    The NQ was originally developed and validated as a phone interview questionnaire to describe the signs and symptoms of breast cancer-related lymphoedema. Participants report subjective differences in the size of the hands, lower arms, and/or upper arms between their right and left sides. For each site difference, the reported score can range from 1 (very slight difference) to 3 (very noticeable difference). The total score can range from 1 (very slight difference at 1 site) to 9 (very noticeable difference at all 3 sites). Higher scores indicate a greater noticeable difference between the two arms

  18. Mean Disability of Arm, Shoulder, Hand Questionnaire (DASH) Scores [At Baseline]

    The DASH is a 30-item self-report questionnaire measuring upper limb symptoms and ability to perform common functional activities in people with musculoskeletal disorders of the upper limb. The disability/symptom questions are scored 1 thru 5, with 1=being no difficulty and 5=being unable to perform. At least 27 of the 30 items must be completed for a scaled score to be calculated. The assigned values for all completed responses are simply summed and averaged, producing a raw score between 1 and 5. This value is then transformed to a score out of 100 to create a DASH disability/symptom score = [(sum of (n) responses) - 1] x 25, where n is equal to the number of completed responses. Each scaled score cut point is scored as 0 (no disability), 25 (mild disability), 50 (moderate), 75 (severe) and 100 (unable to perform activities). Higher scores indicate greater limitation.

  19. Mean Disability of Arm, Shoulder, Hand Questionnaire (DASH) Scores [At 4 weeks]

    The DASH is a 30-item self-report questionnaire measuring upper limb symptoms and ability to perform common functional activities in people with musculoskeletal disorders of the upper limb. The disability/symptom questions are scored 1 thru 5, with 1=being no difficulty and 5=being unable to perform. At least 27 of the 30 items must be completed for a scaled score to be calculated. The assigned values for all completed responses are simply summed and averaged, producing a raw score between 1 and 5. This value is then transformed to a score out of 100 to create a DASH disability/symptom score = [(sum of (n) responses) - 1] x 25, where n is equal to the number of completed responses. Each scaled score cut point is scored as 0 (no disability), 25 (mild disability), 50 (moderate), 75 (severe) and 100 (unable to perform activities). Higher scores indicate greater limitation.

  20. Mean Patient-Reported Outcomes Measurement Information System® (PROMIS) Physical Function for the Upper Extremity (UE) [At Baseline]

    The PROMIS for the Upper Extremity is reliable and addresses disability with physical activities that involve upper limb activities. The instrument items include 5 response options, from 1 "not at all" to 5 "very much." Total scores range from 0 to 100. PROMIS UE scores are scored using a T-score metric, with higher scores indicate higher levels of physical functioning of the upper extremity.

  21. Mean Patient-Reported Outcomes Measurement Information System® (PROMIS) Physical Function for the Upper Extremity (UE) [At 4 weeks]

    The PROMIS for the Upper Extremity is reliable and addresses disability with physical activities that involve upper limb activities. The instrument items include 5 response options, from 1 "not at all" to 5 "very much." Total scores range from 0 to 100. PROMIS UE scores are scored using a T-score metric, with higher scores indicate higher levels of physical functioning of the upper extremity.

  22. Mean Scores on the Participant Version of the Patient-Reported Outcomes Measurement Information System (PROMIS®-29) (Version 2) [At Baseline]

    The PROMIS 29 v2.0 profile assesses pain intensity using a response scale for each item ranging from 0 (no pain) to 10 (worst imaginable pain) on seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social roles and activities, and sleep disturbance), with four items per domain and one question which addresses pain intensity item. PROMIS-29 domains are scored using a T-score metric, with higher scores indicate higher levels of functioning.

  23. Mean Scores on the Participant Version of the Patient-Reported Outcomes Measurement Information System (PROMIS®-29) (Version 2) [At 4 weeks]

    The PROMIS 29 v2.0 profile assesses pain intensity using a response scale for each item ranging from 0 (no pain) to 10 (worst imaginable pain) on seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social roles and activities, and sleep disturbance), with four items per domain and one question which addresses pain intensity item. PROMIS-29 domains are scored using a T-score metric, with higher scores indicate higher levels of functioning.

  24. Mean Functional Assessment of Cancer Therapy-Breast (FACT-B) Scores [At Baseline]

    The FACT-B is a self-report instrument that measures multidimensional quality of life (QOL) in patients with breast cancer. The FACT-B consists of 37 questions that address physical, social, emotional, and functional well-being, with specific questions relevant to women with breast cancer. Each item has a score range of 0 (Not at all) to 4 (Very much), with a total score ranging from 0-148 The higher the score, the better the QOL reported by the participant.

  25. Mean Functional Assessment of Cancer Therapy-Breast (FACT-B) Scores [At 4 weeks]

    The FACT-B is a self-report instrument that measures multidimensional quality of life (QOL) in patients with breast cancer. The FACT-B consists of 37 questions that address physical, social, emotional, and functional well-being, with specific questions relevant to women with breast cancer. Each item has a score range of 0 (Not at all) to 4 (Very much), with a total score ranging from 0-148 The higher the score, the better the QOL reported by the participant.

  26. Mean Body Image Scale (BIS) Score [At baseline]

    The 10-item Body Image Scale was developed by Hopwood et al. in 2001 to measure affective, behavioral, and cognitive body image symptoms. Patients can indicate body image symptoms on a 4-point scale (0 "not at all" to 3 "very much"). The total score ranges from 0 to 30 and can be calculated by summing up the 10 items. A higher score means a higher level of body image disturbance

  27. Mean Body Image Scale (BIS) Score [At 4 weeks]

    The 10-item Body Image Scale was developed by Hopwood et al. in 2001 to measure affective, behavioral, and cognitive body image symptoms. Patients can indicate body image symptoms on a 4-point scale (0 "not at all" to 3 "very much"). The total score ranges from 0 to 30 and can be calculated by summing up the 10 items. A higher score means a higher level of body image disturbance

  28. Mean Functional Assessment of Chronic Illness Therapy (FACIT) - Treatment Satisfaction - General (TSG) Scores [At 4 weeks]

    Satisfaction with treatment will be evaluated at the 4-week assessment using the Functional Assessment of Chronic Illness Therapy (FACIT) - Treatment Satisfaction - General (TSG) (FACIT-TSG- Version 4). The FACIT-TSG is a copyrighted 8-item questionnaire, with each item score ranging from 0 ("not at all") to 4 ("very much"). Total scores range from 0 to 32 with higher scores indicating greater satisfaction with treatment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
INCLUSION CRITERIA:
To be included women must be:

Be over 18 years of age;

Have had cancer treatment that included a surgical procedure, radiation therapy (RT), and/or chemotherapy (CTX);

Have completed active cancer treatment at least 1 year prior to study enrollment;

Have been diagnosed with lymphedema (LE) at least one year prior to study enrollment;

Have arm lymphedema on one side only;

Have confirmed LE based on bioimpedance measurements with an L-Dex® score of >7.1 (note - this is very mild lymphedema);

Have stable arm LE. LE will be considered "stable" if during the 3 months prior to study enrollment there was no arm infection requiring antibiotics, no change in ability to perform activities of daily living related to LE, and no subjective report of significant persistent changes in limb volume;

Be mentally and physically able to participate in the study;

Be able to attend the sessions at the University of California, San Francisco (UCSF) Parnassus campus;

Read and understand English;

Be able to understand a written informed consent document and the willingness to sign it

EXCLUSION CRITERIA

Women cannot have:
  • Bilateral upper extremity LE;

  • Current infection or lymphangitis involving the affected arm;

  • Current recurrence of their breast cancer (BC) (local or distant)

  • Pre-existing LE prior to their BC diagnosis;

  • A condition that precludes measurement of LE using Bioimpedance Spectroscopy (BIS), including pregnancy;

  • Current venous thrombosis in either upper extremity or be on current anticoagulant therapy;

  • Extremity edema due to heart failure

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of California San Francisco San Francisco California United States 94158

Sponsors and Collaborators

  • University of California, San Francisco
  • Foundation for Physical Therapy, Inc.

Investigators

  • Principal Investigator: Betty Smoot, DPTSc, MAS, University of California, San Francisco

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT03252145
Other Study ID Numbers:
  • P0518095
  • NCI-2018-00009
  • 16802
First Posted:
Aug 17, 2017
Last Update Posted:
Jan 15, 2021
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details Participants were recruited from a University of California, San Francisco 5-year cross-sectional study (CA187160). In addition, flyers were made available to participants at lymphedema and breast cancer conferences and patient symposia. Community collaborators (breast surgeons, lymphedema specialists, support group leaders) were also sent informational and recruitment materials related to the study.
Pre-assignment Detail Of the 130 who expressed interest in the study, only 28 met all inclusion criteria.
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Period Title: Overall Study
STARTED 13 15
COMPLETED 11 13
NOT COMPLETED 2 2

Baseline Characteristics

Arm/Group Title Manual Lymph Drainage Negative Pressure Total
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia. Total of all reporting groups
Overall Participants 13 15 28
Age, Customized (Count of Participants)
30-39 years old
1
7.7%
1
6.7%
2
7.1%
40-49 years old
1
7.7%
1
6.7%
2
7.1%
50-59 years old
4
30.8%
4
26.7%
8
28.6%
60-69 years old
5
38.5%
3
20%
8
28.6%
70-79 years old
2
15.4%
5
33.3%
7
25%
80-89 years old
0
0%
1
6.7%
1
3.6%
Sex: Female, Male (Count of Participants)
Female
13
100%
15
100%
28
100%
Male
0
0%
0
0%
0
0%
Ethnicity (NIH/OMB) (Count of Participants)
Hispanic or Latino
1
7.7%
0
0%
1
3.6%
Not Hispanic or Latino
12
92.3%
15
100%
27
96.4%
Unknown or Not Reported
0
0%
0
0%
0
0%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native
0
0%
0
0%
0
0%
Asian
1
7.7%
1
6.7%
2
7.1%
Native Hawaiian or Other Pacific Islander
0
0%
0
0%
0
0%
Black or African American
1
7.7%
3
20%
4
14.3%
White
10
76.9%
11
73.3%
21
75%
More than one race
0
0%
0
0%
0
0%
Unknown or Not Reported
1
7.7%
0
0%
1
3.6%
Region of Enrollment (participants) [Number]
United States
13
100%
15
100%
28
100%

Outcome Measures

1. Primary Outcome
Title Recruitment Rates
Description The recruitment rate is defined as the number of women who were screened and then enrolled on the study divided by the the total number of women screened overall.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Number [rate of recruitment]
32.5
37.5
2. Primary Outcome
Title Percentage of Participants Who Completed All Study Visits
Description Retention rates for both arms of this study were evaluated. The numbers of women who completed the study will be recorded. Reasons for drop out will be ascertained.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Number [percentage of participants]
84.6
650.8%
86.7
578%
3. Secondary Outcome
Title Mean Limb Volume
Description Arm circumferential measurements of both limbs and hands were taken twice, using a spring-loaded tape measure. The hand was measured in two locations. Upper extremity measurements were taken at 10 centimeter (cm) intervals from the ulnar styloid of the wrist up to a total distance of 40 cm. Circumferences were measured using the procedures outlined by Cornish et al. Limb volume was calculated using the formula for volume of a truncated cone and reported in millilitre (ml)
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Mean (Standard Deviation) [ml]
383.32
(324.74)
622.17
(396.39)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.096
Comments
Method t-test, 2 sided
Comments
4. Secondary Outcome
Title Mean Limb Volume
Description Arm circumferential measurements of both limbs and hands were taken twice, using a spring-loaded tape measure. The hand was measured in two locations. Upper extremity measurements were taken at 10 centimeter (cm) intervals from the ulnar styloid of the wrist up to a total distance of 40 cm. Circumferences were measured using the procedures outlined by Cornish et al. Limb volume was calculated using the formula for volume of a truncated cone and reported in millilitre (ml)
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Mean (Standard Deviation) [ml]
352.66
(317.74)
512.98
(332.77)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.206
Comments
Method t-test, 2 sided
Comments
5. Secondary Outcome
Title Mean Lymphedema Index (L-DEX®) Ratio Scores
Description Bioimpedance spectroscopy (BIS) measurements were taken using a single channel BIS, tetrapolar device (LDex device, ImpediMed, San Diego, CA) to evaluate upper limb bioelectrical impedance. Impedance ratios (unaffected/affected limb) are calculated and converted to L-Dex ratio score. With development of lymphedema, impedance of extremity decreases and L-Dex ratio therefore increases. An L-Dex ratio score of 10 is equivalent to impedance ratio of 1.139 (which is = to 3 standard deviations (SD) from mean normative BIS data) for at-risk dominant arms & 1.066 for at-risk non-dominant arms, respectively. Each 1 standard unit in L-Dex is equivalent to impedance ratio of 0.03. Using this arbitrary scale relevant to normative standards, a patient is determined to have arm lymphedema if L-Dex ratio score exceeds 7.1, which is 2 SD above mean normative data for BIS impedance ratios. Higher L-Dex ratio score means higher impedance ratio between limbs, which means more volume in affected limb.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
The range of L-DEX ratio scores on our study at baseline were 0.1 - 74.20.
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Mean (Standard Deviation) [score on a scale]
23.09
(20.87)
34.16
(24.73)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.096
Comments
Method t-test, 2 sided
Comments
6. Secondary Outcome
Title Mean L-DEX® Scores
Description Bioimpedance spectroscopy (BIS) measurements were taken using a single channel BIS, tetrapolar device (LDex device, ImpediMed, San Diego, CA) to evaluate upper limb bioelectrical impedance. Impedance ratios (unaffected/affected limb) are calculated and converted to L-Dex ratio score. With development of lymphedema, impedance of extremity decreases and L-Dex ratio therefore increases. An L-Dex ratio score of 10 is equivalent to impedance ratio of 1.139 (which is = to 3 standard deviations (SD) from mean normative BIS data) for at-risk dominant arms & 1.066 for at-risk non-dominant arms, respectively. Each 1 standard unit in L-Dex is equivalent to impedance ratio of 0.03. Using this arbitrary scale relevant to normative standards, a patient is determined to have arm lymphedema if L-Dex ratio score exceeds 7.1, which is 2 SD above mean normative data for BIS impedance ratios. Higher L-Dex ratio score means higher impedance ratio between limbs, which means more volume in affected limb.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
The range of L-DEX ratio scores on our study at 4 weeks were -2.85 - 77.50.
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Mean (Standard Deviation) [score on a scale]
26.30
(22.23)
30.09
(22.72)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.206
Comments
Method t-test, 2 sided
Comments
7. Secondary Outcome
Title Mean Skin Induration Score
Description The SkinFibroMeter (Delfin Technologies, Finland) was used to measure tissue induration. The SkinFibroMeter consists of a 1 mm long indenter and a force sensor. The device is gently pressed against the skin. The indenter imposes a constant deformation when the reference plate is in full contact with the skin. The skin and the underlying superficial subcutis resist the deformation. Measurements will be taken bilaterally at 5 locations: the first dorsal web space; the medial forearm halfway between the ulnar styloid and medial epicondyle; the lateral forearm halfway between the radial styloid and the lateral epicondyle; the medial arm 3 inches proximal to the medial epicondyle; and the lateral arm 3 inches proximal to the lateral epicondyle. Five recordings were taken at each location and a mean score was calculated.The induration value in Newtons (N) is recorded.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Mean (Standard Deviation) [Newtons]
0.077
(0.023)
0.072
(0.021)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.552
Comments
Method t-test, 2 sided
Comments
8. Secondary Outcome
Title Mean Skin Induration Score
Description The SkinFibroMeter (Delfin Technologies, Finland) was used to measure tissue induration. The SkinFibroMeter consists of a 1 mm long indenter and a force sensor. The device is gently pressed against the skin. The indenter imposes a constant deformation when the reference plate is in full contact with the skin. The skin and the underlying superficial subcutis resist the deformation. Measurements will be taken bilaterally at 5 locations: the first dorsal web space; the medial forearm halfway between the ulnar styloid and medial epicondyle; the lateral forearm halfway between the radial styloid and the lateral epicondyle; the medial arm 3 inches proximal to the medial epicondyle; and the lateral arm 3 inches proximal to the lateral epicondyle. Five recordings were taken at each location and a mean score was calculated.The induration value in Newtons (N) is recorded.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Mean (Standard Deviation) [Newtons]
0.069
(0.017)
0.065
(0.017)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.498
Comments
Method t-test, 2 sided
Comments
9. Secondary Outcome
Title Mean Degrees of Shoulder Range of Motion
Description Active shoulder flexion and abduction range of motion (ROM) was assessed, with patients supine, using a goniometer and standardized procedures reported by Norkin and White. Bilateral ROM was assessed. Two measurements will be taken for each motion and a mean obtained, for each, bilaterally. Findings are recorded in degrees.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Affected arm
167.5
(5.0)
157.1
(34.0)
Unaffected arm
168.5
(6.9)
163.7
(12.7)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Affected Arm Only
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.264
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 2
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Unaffected arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.224
Comments
Method t-test, 2 sided
Comments
10. Secondary Outcome
Title Mean Degrees of Shoulder Range of Motion
Description Active shoulder flexion and abduction range of motion (ROM) was assessed, with patients supine, using a goniometer and standardized procedures reported by Norkin and White. Bilateral ROM was assessed. Two measurements will be taken for each motion and a mean obtained, for each, bilaterally. Findings are recorded in degrees.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Affected arm
170.5
(6.0)
165.5
(9.5)
Unaffected arm
169.3
(7.5)
164.6
(11.6)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Affected arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.125
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 2
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Unaffected arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.241
Comments
Method t-test, 2 sided
Comments
11. Secondary Outcome
Title Mean Grip Score
Description Grip strength was assessed using a Jamar hydraulic hand dynamometer (Patterson Medical, Bolingbrook, IL). Patients will be tested in sitting with the feet flat on the floor, the arm at the side with the elbow flexed to 90 degrees. The patient was instructed to maximally squeeze the handle and hold for a count of 3. The peak-hold needle will automatically record the highest force exerted. Two trials for each extremity will be done and a mean grip score (in kilogram of force) calculated. A higher score indicates a greater grip strength.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Affected Arm
24.0
(4.7)
21.5
(6.4)
Unaffected Arm
25.7
(6.8)
24.5
(4.3)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Affected Arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.261
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 2
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Unaffected Arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.597
Comments
Method t-test, 2 sided
Comments
12. Secondary Outcome
Title Mean Grip Score
Description Grip strength was assessed using a Jamar hydraulic hand dynamometer (Patterson Medical, Bolingbrook, IL). Patients will be tested in sitting with the feet flat on the floor, the arm at the side with the elbow flexed to 90 degrees. The patient was instructed to maximally squeeze the handle and hold for a count of 3. The peak-hold needle will automatically record the highest force exerted. Two trials for each extremity will be done and a mean grip score (in kilograms of force) calculated. A higher score indicates a greater grip strength.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 13 15
Affected arm
26.4
(6.6)
25.2
(4.1)
Unaffected arm
25.5
(6.1)
22.6
(5.5)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Affected arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.596
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 2
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Unaffected arm
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.219
Comments
Method t-test, 2 sided
Comments
13. Secondary Outcome
Title Mean Karnofsky Performance Status (KPS) Score
Description Participants rated their functional status using the single item KPS scale with a range from 0 (dead) to 100 (I feel normal; I have no complaints or symptoms), in increments of 10 (0,10,20, 30 , 40...). The lower the Karnofsky score, the worse the impairment.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 13
Mean (Standard Deviation) [score on a scale]
89.12
(13.79)
88.18
(8.74)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.842
Comments
Method t-test, 2 sided
Comments
14. Secondary Outcome
Title Mean Karnofsky Performance Status (KPS) Score
Description Participants rated their functional status using the single item KPS scale with a range from 0 (dead) to 100 (I feel normal; I have no complaints or symptoms), in increments of 10 (0,10,20, 30 , 40...). The lower the Karnofsky score, the worse the impairment.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 weeks
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 13
Mean (Standard Deviation) [score on a scale]
91.8
(4.04)
90.91
(9.44)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.772
Comments
Method t-test, 2 sided
Comments
15. Secondary Outcome
Title Mean Self-Administered Comorbidity Questionnaire (SCQ) Scores
Description The SCQ consists of 13 common medical conditions that are simplified into language that could be understood without any prior medical knowledge. Patients were asked to indicate if they had the condition using a "yes/no" format. If they indicate that they had a condition, they are asked if they received treatment for it (yes/no; proxy for disease severity) and did it limit their activities (yes/no; indication of functional limitations). • For each condition, a patient can receive a maximum of 3 points. Because there are 13 defined medical conditions and 2 optional conditions, the maximum achievable total score is 45 points as all items were available for use.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 11
Mean (Standard Deviation) [score on a scale]
2.25
(2.09)
3.42
(3.18)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.300
Comments
Method t-test, 2 sided
Comments
16. Secondary Outcome
Title Mean Self-Administered Comorbidity Questionnaire (SCQ) Scores
Description The SCQ consists of 13 common medical conditions that are simplified into language that could be understood without any prior medical knowledge. Patients were asked to indicate if they had the condition using a "yes/no" format. If they indicate that they had a condition, they are asked if they received treatment for it (yes/no; proxy for disease severity) and did it limit their activities (yes/no; indication of functional limitations). • For each condition, a patient can receive a maximum of 3 points. Because there are 13 defined medical conditions and 2 optional conditions, the maximum achievable total score is 45 points as all items were available for use.
Time Frame 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 weeks
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 11
Mean (Standard Deviation) [score on a scale]
2.25
(2.09)
3.42
(3.18)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.300
Comments
Method t-test, 2 sided
Comments
17. Secondary Outcome
Title Mean Norman Questionnaire (NQ) Scores
Description The NQ was originally developed and validated as a phone interview questionnaire to describe the signs and symptoms of breast cancer-related lymphoedema. Participants report subjective differences in the size of the hands, lower arms, and/or upper arms between their right and left sides. For each site difference, the reported score can range from 1 (very slight difference) to 3 (very noticeable difference). The total score can range from 1 (very slight difference at 1 site) to 9 (very noticeable difference at all 3 sites). Higher scores indicate a greater noticeable difference between the two arms
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 11
Mean (Standard Deviation) [score on a scale]
3.83
(2.76)
4.27
(2.20)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.679
Comments
Method t-test, 2 sided
Comments
18. Secondary Outcome
Title Mean Norman Questionnaire (NQ) Scores
Description The NQ was originally developed and validated as a phone interview questionnaire to describe the signs and symptoms of breast cancer-related lymphoedema. Participants report subjective differences in the size of the hands, lower arms, and/or upper arms between their right and left sides. For each site difference, the reported score can range from 1 (very slight difference) to 3 (very noticeable difference). The total score can range from 1 (very slight difference at 1 site) to 9 (very noticeable difference at all 3 sites). Higher scores indicate a greater noticeable difference between the two arms
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 weeks
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 11
Mean (Standard Deviation) [score on a scale]
2.75
(1.87)
4.27
(2.61)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.120
Comments
Method t-test, 2 sided
Comments
19. Secondary Outcome
Title Mean Norman Questionnaire (NQ) Scores
Description The NQ was originally developed and validated as a phone interview questionnaire to describe the signs and symptoms of breast cancer-related lymphoedema. Participants report subjective differences in the size of the hands, lower arms, and/or upper arms between their right and left sides. For each site difference, the reported score can range from 1 (very slight difference) to 3 (very noticeable difference). The total score can range from 1 (very slight difference at 1 site) to 9 (very noticeable difference at all 3 sites). Higher scores indicate a greater noticeable difference between the two arms
Time Frame At 4 months

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 months
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 7 9
Mean (Standard Deviation) [score on a scale]
2.71
(1.89)
4.56
(2.60)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.138
Comments
Method t-test, 2 sided
Comments
20. Secondary Outcome
Title Mean Disability of Arm, Shoulder, Hand Questionnaire (DASH) Scores
Description The DASH is a 30-item self-report questionnaire measuring upper limb symptoms and ability to perform common functional activities in people with musculoskeletal disorders of the upper limb. The disability/symptom questions are scored 1 thru 5, with 1=being no difficulty and 5=being unable to perform. At least 27 of the 30 items must be completed for a scaled score to be calculated. The assigned values for all completed responses are simply summed and averaged, producing a raw score between 1 and 5. This value is then transformed to a score out of 100 to create a DASH disability/symptom score = [(sum of (n) responses) - 1] x 25, where n is equal to the number of completed responses. Each scaled score cut point is scored as 0 (no disability), 25 (mild disability), 50 (moderate), 75 (severe) and 100 (unable to perform activities). Higher scores indicate greater limitation.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 13
Mean (Standard Deviation) [score on a scale]
12.40
(16.83)
21.45
(18.44)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.096
Comments
Method t-test, 2 sided
Comments
21. Secondary Outcome
Title Mean Disability of Arm, Shoulder, Hand Questionnaire (DASH) Scores
Description The DASH is a 30-item self-report questionnaire measuring upper limb symptoms and ability to perform common functional activities in people with musculoskeletal disorders of the upper limb. The disability/symptom questions are scored 1 thru 5, with 1=being no difficulty and 5=being unable to perform. At least 27 of the 30 items must be completed for a scaled score to be calculated. The assigned values for all completed responses are simply summed and averaged, producing a raw score between 1 and 5. This value is then transformed to a score out of 100 to create a DASH disability/symptom score = [(sum of (n) responses) - 1] x 25, where n is equal to the number of completed responses. Each scaled score cut point is scored as 0 (no disability), 25 (mild disability), 50 (moderate), 75 (severe) and 100 (unable to perform activities). Higher scores indicate greater limitation.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 weeks
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 13
Mean (Standard Deviation) [score on a scale]
11.20
(16.03)
17.62
(18.22)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.206
Comments
Method t-test, 2 sided
Comments
22. Secondary Outcome
Title Mean Patient-Reported Outcomes Measurement Information System® (PROMIS) Physical Function for the Upper Extremity (UE)
Description The PROMIS for the Upper Extremity is reliable and addresses disability with physical activities that involve upper limb activities. The instrument items include 5 response options, from 1 "not at all" to 5 "very much." Total scores range from 0 to 100. PROMIS UE scores are scored using a T-score metric, with higher scores indicate higher levels of physical functioning of the upper extremity.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 11 10
Mean (Standard Deviation) [score on a scale]
47.86
(6.26)
44.70
(7.71)
23. Secondary Outcome
Title Mean Patient-Reported Outcomes Measurement Information System® (PROMIS) Physical Function for the Upper Extremity (UE)
Description The PROMIS for the Upper Extremity is reliable and addresses disability with physical activities that involve upper limb activities. The instrument items include 5 response options, from 1 "not at all" to 5 "very much." Total scores range from 0 to 100. PROMIS UE scores are scored using a T-score metric, with higher scores indicate higher levels of physical functioning of the upper extremity.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 weeks
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 11 10
Mean (Standard Deviation) [score on a scale]
49.35
(6.40)
43.14
(8.44)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.080
Comments
Method t-test, 2 sided
Comments
24. Secondary Outcome
Title Mean Scores on the Participant Version of the Patient-Reported Outcomes Measurement Information System (PROMIS®-29) (Version 2)
Description The PROMIS 29 v2.0 profile assesses pain intensity using a response scale for each item ranging from 0 (no pain) to 10 (worst imaginable pain) on seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social roles and activities, and sleep disturbance), with four items per domain and one question which addresses pain intensity item. PROMIS-29 domains are scored using a T-score metric, with higher scores indicate higher levels of functioning.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 11 10
Physical Function
19.4
(1.0)
17.6
(2.6)
Anxiety
6.5
(3.0)
6.8
(3.5)
Depression
5.7
(2.3)
6.5
(3.5)
Fatigue
7.0
(2.7)
9.6
(3.0)
Sleep Disturbance
8.6
(3.3)
10.0
(2.2)
Roles/Activity
18.1
(2.3)
15.1
(3.1)
Pain Interference
4.5
(1.5)
7.5
(2.8)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Physical Function Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.068
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 2
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Anxiety Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.808
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 3
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Depression Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.557
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 4
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Fatigue Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.049
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 5
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Sleep Disturbance Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.279
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 6
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Roles/Activity Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.020
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 7
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Pain Interference Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.009
Comments
Method t-test, 2 sided
Comments
25. Secondary Outcome
Title Mean Scores on the Participant Version of the Patient-Reported Outcomes Measurement Information System (PROMIS®-29) (Version 2)
Description The PROMIS 29 v2.0 profile assesses pain intensity using a response scale for each item ranging from 0 (no pain) to 10 (worst imaginable pain) on seven health domains (physical function, fatigue, pain interference, depressive symptoms, anxiety, ability to participate in social roles and activities, and sleep disturbance), with four items per domain and one question which addresses pain intensity item. PROMIS-29 domains are scored using a T-score metric, with higher scores indicate higher levels of functioning.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at 4 weeks
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 11 9
Physical Function
19.8
(0.40)
17.2
(3.4)
Anxiety
4.9
(1.3)
6.7
(3.0)
Depression
4.5
(1.0)
5.1
(2.2)
Fatigue
6.5
(2.8)
8.9
(3.2)
Sleep Disturbance
8.0
(3.1)
10.4
(4.1)
Roles/Activity
18.5
(2.4)
13.9
(3.9)
Pain Interference
4.9
(1.4)
7.9
(4.0)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Physical Function Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.038
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 2
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Anxiety Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.108
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 3
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Depression Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.467
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 4
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Fatigue Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.078
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 5
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Sleep Disturbance Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.147
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 6
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Roles/Activity Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.004
Comments
Method t-test, 2 sided
Comments
Statistical Analysis 7
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments Pain Interference Domain
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.032
Comments
Method t-test, 2 sided
Comments
26. Secondary Outcome
Title Mean Functional Assessment of Cancer Therapy-Breast (FACT-B) Scores
Description The FACT-B is a self-report instrument that measures multidimensional quality of life (QOL) in patients with breast cancer. The FACT-B consists of 37 questions that address physical, social, emotional, and functional well-being, with specific questions relevant to women with breast cancer. Each item has a score range of 0 (Not at all) to 4 (Very much), with a total score ranging from 0-148 The higher the score, the better the QOL reported by the participant.
Time Frame At Baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 14
Mean (Standard Deviation) [score on a scale]
114.3
(21.8)
113.6
(21.1)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.938
Comments
Method t-test, 2 sided
Comments
27. Secondary Outcome
Title Mean Functional Assessment of Cancer Therapy-Breast (FACT-B) Scores
Description The FACT-B is a self-report instrument that measures multidimensional quality of life (QOL) in patients with breast cancer. The FACT-B consists of 37 questions that address physical, social, emotional, and functional well-being, with specific questions relevant to women with breast cancer. Each item has a score range of 0 (Not at all) to 4 (Very much), with a total score ranging from 0-148 The higher the score, the better the QOL reported by the participant.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at week 4
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 14
Mean (Standard Deviation) [score on a scale]
118.4
(14.4)
114.7
(18.8)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.603
Comments
Method t-test, 2 sided
Comments
28. Secondary Outcome
Title Mean Body Image Scale (BIS) Score
Description The 10-item Body Image Scale was developed by Hopwood et al. in 2001 to measure affective, behavioral, and cognitive body image symptoms. Patients can indicate body image symptoms on a 4-point scale (0 "not at all" to 3 "very much"). The total score ranges from 0 to 30 and can be calculated by summing up the 10 items. A higher score means a higher level of body image disturbance
Time Frame At baseline

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the assessment at baseline
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 13
Mean (Standard Deviation) [score on a scale]
8.8
(6.6)
9.4
(8.4)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.837
Comments
Method t-test, 2 sided
Comments
29. Secondary Outcome
Title Mean Body Image Scale (BIS) Score
Description The 10-item Body Image Scale was developed by Hopwood et al. in 2001 to measure affective, behavioral, and cognitive body image symptoms. Patients can indicate body image symptoms on a 4-point scale (0 "not at all" to 3 "very much"). The total score ranges from 0 to 30 and can be calculated by summing up the 10 items. A higher score means a higher level of body image disturbance
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
Only a subset of participants completed the questionnaire at week 4
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 13
Mean (Standard Deviation) [score on a scale]
7.7
(6.4)
9.5
(7.5)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.511
Comments
Method t-test, 2 sided
Comments
30. Secondary Outcome
Title Mean Functional Assessment of Chronic Illness Therapy (FACIT) - Treatment Satisfaction - General (TSG) Scores
Description Satisfaction with treatment will be evaluated at the 4-week assessment using the Functional Assessment of Chronic Illness Therapy (FACIT) - Treatment Satisfaction - General (TSG) (FACIT-TSG- Version 4). The FACIT-TSG is a copyrighted 8-item questionnaire, with each item score ranging from 0 ("not at all") to 4 ("very much"). Total scores range from 0 to 32 with higher scores indicating greater satisfaction with treatment.
Time Frame At 4 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
Measure Participants 12 10
Mean (Standard Deviation) [score on a scale]
24.6
(5.9)
27.0
(5.2)
Statistical Analysis 1
Statistical Analysis Overview Comparison Group Selection Manual Lymph Drainage, Negative Pressure
Comments
Type of Statistical Test Other
Comments
Statistical Test of Hypothesis p-Value 0.326
Comments
Method t-test, 2 sided
Comments

Adverse Events

Time Frame Up to 4 weeks
Adverse Event Reporting Description
Arm/Group Title Manual Lymph Drainage Negative Pressure
Arm/Group Description Manual lymph drainage (MLD) treatment 3 times a week for 4 weeks to the lymphedematous upper limb Manual Lymph Drainage (MLD): MLD is a practitioner-applied manual massage technique designed to decrease limb volume in patients with lymphedema by enhancing movement of lymph fluid, resulting in reductions in interstitial fluid. PhysioTouch (negative pressure massage) treatment 3 times a week for 4 weeks to the lymphedematous upper limb PhysioTouch: The PhysioTouch is a hand-held device that administers negative pressure under the treatment head, and gently pulls the underlying skin and subcutaneous tissue into the suction cup. This suction produces a stretch to the skin and in the subcutaneous tissue space. This action is thought to facilitate lymphatic flow from the interstitium into the lymphatic vessels, and mobilizes the superficial fascia.
All Cause Mortality
Manual Lymph Drainage Negative Pressure
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/13 (0%) 0/15 (0%)
Serious Adverse Events
Manual Lymph Drainage Negative Pressure
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/13 (0%) 0/15 (0%)
Other (Not Including Serious) Adverse Events
Manual Lymph Drainage Negative Pressure
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 1/13 (7.7%) 4/15 (26.7%)
General disorders
Limb Pain 0/13 (0%) 0 1/15 (6.7%) 1
Shoulder/Neck Pain 0/13 (0%) 0 1/15 (6.7%) 1
Injury, poisoning and procedural complications
Elbow Fracture 0/13 (0%) 0 1/15 (6.7%) 1
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Leukemia 1/13 (7.7%) 1 0/15 (0%) 0
Skin and subcutaneous tissue disorders
Cellulitis 0/13 (0%) 0 1/15 (6.7%) 1

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Betty Smoot, DPTSc, PT
Organization University of California, San Francisco
Phone (707) 494-8262
Email Betty.Smoot@ucsf.edu
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT03252145
Other Study ID Numbers:
  • P0518095
  • NCI-2018-00009
  • 16802
First Posted:
Aug 17, 2017
Last Update Posted:
Jan 15, 2021
Last Verified:
Dec 1, 2020