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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05188157
Other study ID # MLeblebicier2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 14, 2022
Est. completion date March 1, 2022

Study information

Verified date December 2021
Source Kutahya Health Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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).


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date March 1, 2022
Est. primary completion date February 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
mirror therapy
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.
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.

Locations

Country Name City State
Turkey Kutahya Health Science University Kutahya

Sponsors (1)

Lead Sponsor Collaborator
Kutahya Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary goniometer shoulder range of motion and will be measured 10 minutes
Primary Hawkins test impingement tests; forced internal rotation was performed while the arm and elbow were in 90° flexion 5 minutes
Primary Neer test subacromial impingement test 5 minutes
Primary Jobe Test lesions of the infraspinatus muscle 5 minutes
Primary Constant Murley Score functional level of the patients' shoulder joint, higher scores mean a better outcome. 10 minutes
Primary Tampa Kinesiophobia Scale will be used to evaluate kinesiophobia, higher scores mean worse outcome. 10 minutes
See also
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Completed NCT04579003 - Mobilization and Mobilization With Movement Effect on Sub Acromial Space in Impingement Syndrome. N/A