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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02286310
Other study ID # GO14-189
Secondary ID
Status Recruiting
Phase N/A
First received November 2, 2014
Last updated November 6, 2014
Start date February 2014
Est. completion date February 2016

Study information

Verified date November 2014
Source Hacettepe University
Contact Elif Turgut, MSc
Phone 00903123052525
Email elifcamci@hacettepe.edu.tr
Is FDA regulated No
Health authority Turkey: Ethics CommitteeTurkey: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the effect of exercise program on 3-dimensional scapular kinematics, disability and pain on shoulder impingement with scapular dyskinesia.


Recruitment information / eligibility

Status Recruiting
Enrollment 36
Est. completion date February 2016
Est. primary completion date February 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Subacromial impingement with scapular dyskinesia

Exclusion Criteria:

- Additional muscular and skeletal or systemic diseases

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Kinetic Chain Exercises
Exercises include kinetic chain segments.
Traditional Exercises
Stretching, strengthening exercises.

Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 3-Dimensional Scapular Kinematics measured by electromagnetic tracking system Scapular rotations and orientations in degrees Change from Baseline in Angular Data at 1 year No
Secondary Pain and Disability Status measured by Shoulder Pain and Disability Index (SPADI) Scoring with patient-reported outcome measure Change from Baseline in Scor at 1 year No
Secondary Pain Severity measured by Visual Analogue Scale (in millimeters) Scale is in millimeters Change from Baseline in Pain Severity at 1 year No
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