Mirror Therapy for Impingement Syndrome

Sponsor
Kutahya Health Sciences University (Other)
Overall Status
Completed
CT.gov ID
NCT05188157
Collaborator
(none)
62
1
2
1.5
41

Study Details

Study Description

Brief 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).

Condition or Disease Intervention/Treatment Phase
  • Other: mirror therapy
  • Other: conventional physiotherapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
62 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Mirror Therapy is an Adjuvant Treatment Option Based on Shoulder Impingement Syndrome.
Actual Study Start Date :
Jan 14, 2022
Actual Primary Completion Date :
Feb 15, 2022
Actual Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: control group

conventional physiotherapy

Other: 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

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.

Other: 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.

Outcome Measures

Primary Outcome Measures

  1. goniometer [10 minutes]

    shoulder range of motion and will be measured

  2. Hawkins test [5 minutes]

    impingement tests; forced internal rotation was performed while the arm and elbow were in 90° flexion

  3. Neer test [5 minutes]

    subacromial impingement test

  4. Jobe Test [5 minutes]

    lesions of the infraspinatus muscle

  5. Constant Murley Score [10 minutes]

    functional level of the patients' shoulder joint, higher scores mean a better outcome.

  6. Tampa Kinesiophobia Scale [10 minutes]

    will be used to evaluate kinesiophobia, higher scores mean worse outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kutahya Health Science University Kutahya Turkey 43000

Sponsors and Collaborators

  • Kutahya Health Sciences University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kutahya Health Sciences University
ClinicalTrials.gov Identifier:
NCT05188157
Other Study ID Numbers:
  • MLeblebicier2
First Posted:
Jan 12, 2022
Last Update Posted:
Jun 1, 2022
Last Verified:
Dec 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Kutahya Health Sciences University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 1, 2022