PROTECT: Shoulder Prosthesis Telerehab Care Trial

Sponsor
University Hospital, Ghent (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05699031
Collaborator
University Ghent (Other)
120
2
43

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to compare the rehabilitation by use of a smartphone-app with the usual care of physical therapy in patients, 60 years and older, who underwent a primary shoulder arthroplasty.

The main questions it aims to answer are:
  • is the outcome of rehabilitation with the app as good as the usual care?

  • is the outcome for both types of shoulder arthroplasty similar?

  • what is the usability of the app?.

Participants will

  • have treatment according to the group they are allocated to

  • fill in questionnaires at specific moments during the rehabilitation stage (0 - 3 months ) and at 1 year post-surgery

Condition or Disease Intervention/Treatment Phase
  • Device: APP
  • Other: PHYSICAL THERAPY
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The PROTECT-study: Home-based Telerehabilitation in the Post-operative Care After Shoulder Arthroplasty Compared to Usual Care: a Randomized Control Trial
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Sep 30, 2026
Anticipated Study Completion Date :
Sep 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: APP-GROUP

Patients allocated in the app-group will use the app to rehabilitate.

Device: APP
Patients allocated in the app-group will use the newly developed smartphone app te rehabilitate. 5 exercises are provided daily. Daily questionnaires will monitor exercise performance, VAS pain, household activities. Information modules will be sent at specific times.

Active Comparator: PHYSIO-GROUP

Patients allocated in the physio-group will rehabilitate according to the usual care protocol

Other: PHYSICAL THERAPY
Patients allocated in the physio-group will go, twice a week, to a physical therapist of their choice to rehabilitate. The physical therapist will follow the general guidelines provided by the hospital (surgeon).
Other Names:
  • PHYSIO-GROUP
  • Outcome Measures

    Primary Outcome Measures

    1. SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline pre-operative [Prior to surgery]

      Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

    2. SHOULDER PAIN AND DISABILITY INDEX (SPADI)_baseline post-operative [week 0]

      Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

    3. SHOULDER PAIN AND DISABILITY INDEX (SPADI) [week 3]

      Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

    4. SHOULDER PAIN AND DISABILITY INDEX (SPADI) [week 6]

      Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

    5. SHOULDER PAIN AND DISABILITY INDEX (SPADI) [week 12]

      Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

    6. SHOULDER PAIN AND DISABILITY INDEX (SPADI) [week 52]

      Content: 5 questions for the subscale pain and 8 questions for the disability subscale. Scoring: numeric rating scale from 1 to 10, with a maximum of 130. The total score is the sum of the sub-scores. Interpretation: The higher the score the more pain and disability. The lower the score, the better patients perceive their shoulder

    Secondary Outcome Measures

    1. ACTIVE MOBILITY (ROM) OF THE SHOULDER [Prior to surgery, week 3, week 6, week 12, week 52]

      ACTIVE ROM: forward flexion and abduction with extended elbow, functional internal and external rotation in standing position. maximal pain free ROM forward flexion and abduction with extended elbow: measured with the EasyAngle (Meloq AB Sweden) hand-to-back and hand-nek test : scored as in Constant-Murley Score 2) PASSIVE: forward flexion, abduction, external and internal rotation in supine position. maximal pain free ROM forward flexion and abduction: measured with the EasyAngle (Meloq AB Sweden) rotations: measured as ER1 (arm at the side)/ ER2 (arm in 90° abduction) and IR1 (arm in 90° forward flexion)/ IR2 (arm in 90° abduction) with the EasyAngle (Meloq AB Sweden).

    2. PASSIVE MOBILITY (ROM) OF THE SHOULDER [Prior to surgery, week 3, week 6, week 12, week 52]

      PASSIVE: forward flexion, abduction, external and internal rotation in supine position. maximal pain free ROM forward flexion and abduction: measured with the EasyAngle (Meloq AB Sweden) rotations: measured as ER1 (arm at the side)/ ER2 (arm in 90° abduction) and IR1 (arm in 90° forward flexion)/ IR2 (arm in 90° abduction) with the EasyAngle (Meloq AB Sweden).

    3. STRENGTH [Prior to surgery, week 3, week 6, week 12, week 52]

      Forward flexion, extension, ab- and adduction, external and internal rotation. isometrical contraction for 5 seconds, 3 repetitions, 30 sec break in between measured with EasyForce (Meloq AB Sweden) seated, both feet on the ground, back against backrest elbow flexed (90°) held at side, fist forward, thumb upward

    4. CONSTANT-MURLEY SCORE [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: partially clinical (65 points) and partially PROM (35 points) assessed. Scoring: The formula to calculate the total score is:" pain (0-15) + ADL (4x (0-5) = 0-20) + mobility (4 x (0-10) = 0-40) + strength (0 -25)". Strength will be measured with the arm elevated to 90 ° in the scapular plane using an IDOmeter. Interpretation: 0-55 points = bad, 56-70 points = mediocre, 71-85 points = good, 86-100 points = excellent score

    5. ACTIVITIES OF DAILY LIVING EXTERNAL AND INTERNAL ROTATIONS (ADLEIR) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: 12 questions about specific ADL tasks that require external or internal rotation while performing. Scoring: Each activity is scored between 0 (unable to do) and 3 (not difficult at all). All activities should be performed without the help of flexing the neck or bending the trunk and without the help of first abducting the elbow (i.e., without doing a hornblower sign). Interpretation: The maximal score is 36. A higher score means that the patient is able to perform ADL activities with enough strength in external and internal rotation

    6. SINGLE ASSESSMENT NUMERIC EVALUATION (SANE) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: 1 question: 'how would you rate your shoulder today as a percentage of normal?'. Scoring: percentage between 0 and 100% Interpretation: 100% being a normal shoulder.

    7. EUROQOL 5-DIMENSIONS 5-LEVEL (EQ-5D-5L) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: 5 questions + EQ-5D VAS for general health. Scoring: 5-response scale (from 'no problems' to 'extreme problems') + VAS percentage between 0 (worst imaginable health state) and 100 (best imaginable health state). Interpretation: VAS score for general health indicates how a patient perceives his general health, Other questions are descriptive for problems in mobility, self-care, usual activities, pain/ discomfort, anxiety/depression.

    8. GRONINGEN ACTIVITY RESTRICTION SCALE (GARS-4) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: 18 questions to identify problems with self-sufficiency in self-care and housekeeping. Patients do not respond if they do that activity but rather if they could do that activity. Scoring: ordinal scale from 1 (Yes, I can do that on my own without any effort) up to 4 (No, I can't do that on my own, but only with the help of others). Interpretation: A higher score (max 72) is related to a lower self-sufficiency.

    9. EXERCISE ADHERENCE RATING SCALE (EARS) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: 3 sections section A: 6 questions to evaluate the prescribed exercises. section B: 6 questions on how a patient does the recommended exercises or activities. section C: 10 statements on why a patient does or does not do the recommended exercises or activities. Scoring: sections B and C: 5-point Likert scale (0 - 4) (some questions scored reversed). Interpretation: section B (range 0 - 24): a higher score indicates a better compliance/adherence . section C (range 0 - 40): a higher score indicates a better adherence.

    10. EXERCISE DIARY [Daily post-surgery (week 0 - week 12)]

      Content: performed exercises, household activities, VAS pain. Diary on paper for physio-group, by the app for the app-group.

    11. SELF-EFFICACY FOR EXERCISES (SEE) [Week 3, week 6, week 12, week 52]

      Content: 9 questions about 'confidence in engaging in exercise 3 times a week for 20 minutes if faced with a barrier'. Scoring: 'not very confident' (0) and 'very confident' (10). Interpretation: The higher the score , the patient feel more confident in performing prescribed exercises.

    12. GLOBAL RATING OF CHANGE SCALE (GROC) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: A single question (How would you currently describe the change in your operated shoulder compared to just before surgery) is scored on a scale, ranging from 'very much worse' through 'unchanged' to 'completely recovered'. Scoring: The scale used is divided in 11 points ( very much worse -5, the same 0, very much better + 5) Interpretation: the number given indicates how a patient perceives the change after surgery.

    13. GLOBAL PERCEIVED EFFECT (GPE/GEE) [Prior to surgery, week 3, week 6, week 12, week 52]

      Content: 2 questions: To what extent have you recovered from your symptoms?, How satisfied are you with your treatment?. Scoring: a 7-point rating scale. Interpretation: The higher the score , the better.

    Other Outcome Measures

    1. M-HEALTH APP USABILITY QUESTIONNAIRE (MAUQ) [Week 12]

      Content: 21 questions in 3 categories: ease of use and satisfaction, system information arrangement, usefulness (version for interactive app, user patient and provider). Scoring: between 1 (strongly disagree) and 7 (strongly agree) => average score. Interpretation: the higher the score the higher the usability.

    2. SYSTEM USABILITY SCALE (SUS) [Week 12]

      Content: 10 questions about system satisfaction, usability and learnability. Scoring: 5 response options ranging from strongly disagree (1) to strongly agree (5). Interpretation: A score above 68 (/100) is considered above average, while a score lower than 68 is considered a below average score.

    3. SINGLE EASE QUESTION (SEQ) [Week 12]

      Content: 1 question to assess how difficult users find a task. Scoring: 7-point rating scale ranging from very difficult (1) to very easy (7). Interpretation: The average SEQ score is 5.5 (between 5.3 and 5.6). It is advised to ask a more detailed information/ explanation if a score <5 is given.

    4. AGE [Pre-surgery]

      Content: specify age of participant

    5. GENDER [Pre-surgery]

      Content: specify gender of participant

    6. DIAGNOSTICS [Pre-surgery]

      Content: specify why patient needed a shoulder arthroplasty

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 60 years and older

    • primary total shoulder arthroplasty (anatomical and reverse)

    • osteoarthritis, cuff tear arthropathy, pseudoparalysis

    • return home after discharge from hospital

    • no brace after surgery

    • sufficient verbal and written comprehension

    • hospitalization insurance

    Exclusion Criteria:
    • revision arthroplasty

    • arthroplasty for fracture or tumor

    • neurological disease (parkinson, stroke, ...)

    • no access to smartphone, tablet or internet connectivity

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University Hospital, Ghent
    • University Ghent

    Investigators

    • Principal Investigator: Alexander Van Tongel, PhD, University Ghent, University Hospital Ghent
    • Study Chair: Ann Cools, PhD, University Ghent

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Ghent
    ClinicalTrials.gov Identifier:
    NCT05699031
    Other Study ID Numbers:
    • ONZ-2022-0357
    First Posted:
    Jan 26, 2023
    Last Update Posted:
    Jan 26, 2023
    Last Verified:
    Jan 1, 2023
    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:
    No
    Keywords provided by University Hospital, Ghent

    Study Results

    No Results Posted as of Jan 26, 2023