The Effect of Mirror Therapy in Patients With Frozen Shoulder

Sponsor
Marmara University (Other)
Overall Status
Completed
CT.gov ID
NCT04454632
Collaborator
(none)
36
1
3
16.3
2.2

Study Details

Study Description

Brief Summary

The aim of this study compares mirror therapy and visual feedback treatment with the control group in frozen shoulder patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Mirror therapy
  • Other: Visual feedback
N/A

Detailed Description

Thirty-six individuals divided three groups as mirror therapy, visual feedback, and control groups were included in the study for 15 sessions of treatment. All individuals received basic treatment as ultrasound, transcutaneous electrical nerve stimulation, cold pack, stretching exercises, glenohumeral range of motion exercises, scapulothoracic exercises. The mirror group bilateral exercised with an affected arm behind the mirror; visual feedback group bilateral exercised by seeing both arms in the mirror; control group bilateral exercised without a mirror for 10 minutes after every session. Pain severity was evaluated with the "Visual Analogue Scale (VAS)", ROM and proprioception were measured with a universal goniometer, and functional status was evaluated with "shoulder pain and disability index (SPADI)" and "Modified Constant Score". Evaluations were made before, day after the treatment and 4 weeks after the treatment by the same researcher. Data analysis was performed with SPSS.23.

Study Design

Study Type:
Interventional
Actual Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Examination of the Effectiveness of Mirror Therapy in the Treatment of Patients With Frozen Shoulder: A Prospective Randomized Controlled Study
Actual Study Start Date :
Feb 15, 2018
Actual Primary Completion Date :
May 29, 2019
Actual Study Completion Date :
Jun 27, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mirror therapy group

The number of participants in this group is anticipated to be 12. In addition to basic treatment, the mirror therapy group bilateral exercised with the affected arm behind the mirror for 10 minutes after every session. Participants in this group perform three exercises as glenohumeral flexion, abduction, and rotation.

Other: Mirror therapy
affected arm stay behind the mirror while exercising

Experimental: Visual feedback group

The number of participants in this group is anticipated to be 12. In addition to basic treatment, the visual feedback group bilateral exercised by seeing both arms in the mirror for 10 minutes after every session. Participants in this group perform three exercises as glenohumeral flexion, abduction, and rotation while seeing both arms in the mirror.

Other: Visual feedback
visual feedback from mirror

No Intervention: Control group

The number of participants in this group is anticipated to be 12. In addition to basic treatment, the control group bilateral exercised without a mirror for 10 minutes after every session. Participants in this group perform three exercises as glenohumeral flexion, abduction, and rotation while seeing both arms in the mirror.

Outcome Measures

Primary Outcome Measures

  1. Visual Analog Scale (VAS) [Change from Baseline, 6 weeks and 10 weeks]

    Pain intensity was obtained using a Visual Analog Scale (VAS). VAS is usually a horizontal line, 10 cm in length, anchored by word descriptors at each end with "No Pain" (score of zero) on the left side up to "severe pain" on the right side. The patient was asked to mark the line point that represented his or her worst pain in the past week during daily rutine.

  2. Range of Motion (ROM) [Change from Baseline, 6 weeks and 10 weeks]

    Range of motion is the measurement of the amount of movement around a joint as a flexion, abduction, external rotation and internal rotation (degree). Measurement performed with universal goniometer.

  3. Proprioception [Change from Baseline, 6 weeks and 10 weeks]

    Proprioception is the sense of self-movement and body position. A joint position error test (JPET) was used for proprioception measurement. JPET is a deviation of the ability to reposition the joint to the target position which fifty percent of active flexion ROM.

  4. Shoulder Pain and Disability Index (SPADI) [Change from Baseline, 6 weeks and 10 weeks]

    The shoulder pain and disability index is a self-administered questionnaire that consists of two dimensions, one for pain and the other one for functional activities on the shoulder. The total score is defining as a percent. 0 for best score 100 for worst score.

  5. Modified Constant-Murley Score (CMS) [Change from Baseline, 6 weeks and 10 weeks]

    The modified Constant-Murley score is a questionnaire for shoulder injuries that consists of four dimensions, pain, activities of daily living, range of movement, and power. Pain and activities of daily living are considered subjective scores therefore the range of movement and power considered objective score. 100 for best score 0 for worst score.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Individuals who were diagnosed with "Unilateral Frozen Shoulder" by the specialist;

  • Normal radiological imaging;

  • Aged between 18-75 years old;

  • Symptoms persist for 2-12 months.

Exclusion Criteria:
  • If patients had following comorbidities: rotator cuff injury, cervical radiculopathy, romatological diseases, neurological diseases, fracture, tumour, congenital deformities, dislocation or sublocation, surgery in the shoulder, uncontrolled hypertension or diabetes mellitus;

  • Pregnancy;

  • Patients who had previously received physical therapy;

  • Patients having problems in the perception of tests and exercises were excluded from this study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dr. Lutfi Kirdar City Hospital Istanbul Kartal Turkey 34865

Sponsors and Collaborators

  • Marmara University

Investigators

  • Study Director: TUGBA KURU ÇOLAK, Assoc. Prof., Marmara University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Marmara University
ClinicalTrials.gov Identifier:
NCT04454632
Other Study ID Numbers:
  • Dr. Lutfi Kirdar Hospital
First Posted:
Jul 1, 2020
Last Update Posted:
Jun 10, 2021
Last Verified:
Jun 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Marmara University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 10, 2021