- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05188157
Mirror Therapy for Impingement Syndrome
May 30, 2022 updated by: Kutahya Health Sciences University
Mirror Therapy is an Adjuvant Treatment Option Based on Shoulder Impingement Syndrome.
Background: Mirror therapy is an adjuvant treatment option based on shoulder impingement Syndrome Objective:To investigate the effect of mirror theraphy on shoulder impingement Syndrome Methods: The study included 62 participants, including cases in the intervention group (IG) (± years) and 20 cases in the control group (CG) (years) who met the selection criteria.
IG received mirror theraphy with regular physiotherapy while CG received only regular physiotherapy.
The patients were evaluated with the before treatment, immediately after treatment (post-treatment).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
62
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Kutahya, Turkey, 43000
- Kütahya Health Science University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being aged 18-75 years
- Being diagnosed with shoulder impingement syndrome
Exclusion Criteria:
- Being uncooperative
- Having an additional systemic disease
- Having uncontrolled hypertension
- Presence of heart failure
- Having hearing or vision problems
- Having a balance disorder
- Diagnosis of heart disease and lung disease so advanced that exercise is contraindicated
- History of shoulder surgery
- Have any pathology that may cause referred pain (eg, cervical radiculopathy)
- Shoulder trauma, previous humeral fracture history
- Steroid injection to the shoulder joint or subacromial bursa in the last 6 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: control group
conventional physiotherapy
|
The conventional physiotherapy program included, wand exercises for shoulder abduction, flexion, hyperextension and internal and external rotation, Codman exercises and isometric and resistive exercises of the shoulder girdle.
The exercise program is performed under the supervision of an experienced physiotherapist.
The isometric exercises will be used during the painful period, and the resistance exercises will be added after the pain began to relieve.under the supervision of a physician in the first 30 minutes of their exercise.
|
Experimental: mirror therapy group
conventional physiotherapy and mirror therapy
|
The conventional physiotherapy program included, wand exercises for shoulder abduction, flexion, hyperextension and internal and external rotation, Codman exercises and isometric and resistive exercises of the shoulder girdle.
The exercise program is performed under the supervision of an experienced physiotherapist.
The isometric exercises will be used during the painful period, and the resistance exercises will be added after the pain began to relieve.under the supervision of a physician in the first 30 minutes of their exercise.
The patients in IG will receive exercise program before mirror theraphy.
The patient will continue to do the exercises in front of the mirror for the remaining 20 minutes of the exercise.
While doing the exercise with the healthy side in front of the mirror, the patient will try to do the same movement with the shoulder diagnosed with impingement syndrome on the other side of the mirror.
The patient will try to do the movement correctly with the reflection in the mirror.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
goniometer
Time Frame: 10 minutes
|
shoulder range of motion and will be measured
|
10 minutes
|
Hawkins test
Time Frame: 5 minutes
|
impingement tests; forced internal rotation was performed while the arm and elbow were in 90° flexion
|
5 minutes
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Neer test
Time Frame: 5 minutes
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subacromial impingement test
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5 minutes
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Jobe Test
Time Frame: 5 minutes
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lesions of the infraspinatus muscle
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5 minutes
|
Constant Murley Score
Time Frame: 10 minutes
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functional level of the patients' shoulder joint, higher scores mean a better outcome.
|
10 minutes
|
Tampa Kinesiophobia Scale
Time Frame: 10 minutes
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will be used to evaluate kinesiophobia, higher scores mean worse outcome.
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 14, 2022
Primary Completion (Actual)
February 15, 2022
Study Completion (Actual)
March 1, 2022
Study Registration Dates
First Submitted
December 27, 2021
First Submitted That Met QC Criteria
December 27, 2021
First Posted (Actual)
January 12, 2022
Study Record Updates
Last Update Posted (Actual)
June 1, 2022
Last Update Submitted That Met QC Criteria
May 30, 2022
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MLeblebicier2
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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