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

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

      • Kutahya, Turkey, 43000
        • Kütahya Health Science University

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
Neer test
Time Frame: 5 minutes
subacromial impingement test
5 minutes
Jobe Test
Time Frame: 5 minutes
lesions of the infraspinatus muscle
5 minutes
Constant Murley Score
Time Frame: 10 minutes
functional level of the patients' shoulder joint, higher scores mean a better outcome.
10 minutes
Tampa Kinesiophobia Scale
Time Frame: 10 minutes
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

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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