- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06890000
Effectiveness of Scapular Exercises Compared to Conventional Treatment in Shoulder Pain
Effectiveness of Scapular Exercises Compared to Conventional Treatment in People with Shoulder Pain: a Randomized Controlled Study
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mehmet DELEN, PhD
- Phone Number: +905548258720
- Email: mehmetdelen@aybu.edu.tr
Study Locations
-
-
-
Ankara, Turkey, 06010
- Recruiting
- Universtiy of Health Sciences - Gülhane Faculty of Physiotherapy and Rehabilitation
-
Contact:
- Mehmet Delen, PhD
- Phone Number: +905548258720
- Email: mehmetdelen@yabu.edu.tr
-
Contact:
- Mehmet DELEN, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having shoulder pain for at least 1 month
- Having obvious scapular dyskinesia
- Having a shoulder ROM (range of motion) at least 120º
- Being 18 years of age or older
Exclusion Criteria:
- Having received any shoulder treatment in the last 6 months
- Having an acromioclavicular joint problem
- Having a diagnosis of frozen shoulder
- Having a fracture in the shoulder area
- Having a major rotator cuff muscle tear
- Having a diagnosis of calcific rotator cuff tendinopathy
- Having a neurological or rheumatological disease
Study Plan
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 |
|---|---|
|
Experimental: Scapular Exercises
Scapular exercise includes scapular clock exercise, rowing exercise, resisted external rotation, resisted punching exercise. The group program also includes conventional treatment. |
Scapular exercise includes scapular clock exercise (3 sets of 10 repetitions), rowing exercise (3 sets of 10 repetitions), resisted external rotation (3 sets of 10 repetitions), resisted punching exercise (3 sets of 10 repetitions). The rowing, external rotation and punching exercises will do with theraband. When participants complete the elastic band exercises easily and do not report any muscle fatigue, they will move on to the next level of difficulty. The color order of the bands is yellow, red, green and blue. The exercises will begin with the yellow elastic band, which provides the least resistance. The intervention will last for 6 weeks, with 2 training sessions per week and each training session lasting 15-20 minutes. Conventional Treatment includes TENS (100 Hz) with hotpack (20 minutes), Stretching exercises (posterior capsule and pectoral muscle), resisted flexion and abduction exercises. The rowing, external rotation and punching exercises will do with theraband. When participants complete the elastic band exercises easily and do not report any muscle fatigue, they will move on to the next level of difficulty. The color order of the bands is yellow, red, green and blue. The exercises will begin with the yellow elastic band, which provides the least resistance. The intervention will last for 6 weeks, with 2 training sessions per week and each training session lasting 30-45 minutes. |
|
Active Comparator: Conventional Treatment
Conventional treatment includes TENS, hotpack, Stretching exercises (posterior capsule and pectoral muscle), resisted flexion and abduction exercises
|
Conventional Treatment includes TENS (100 Hz) with hotpack (20 minutes), Stretching exercises (posterior capsule and pectoral muscle), resisted flexion and abduction exercises. The rowing, external rotation and punching exercises will do with theraband. When participants complete the elastic band exercises easily and do not report any muscle fatigue, they will move on to the next level of difficulty. The color order of the bands is yellow, red, green and blue. The exercises will begin with the yellow elastic band, which provides the least resistance. The intervention will last for 6 weeks, with 2 training sessions per week and each training session lasting 30-45 minutes. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
shoulder pain and disability index (SPADI)
Time Frame: Baseline and at 6 week
|
SPADI is a self reported outcome for shoulder disorders.
SPADI includes 13 questions.
Scores range from 0 to 100.
The higher a patient scores on the SPADI, the greater the level of pain/disability.
|
Baseline and at 6 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Global Rate of Change
Time Frame: Baseline and at 6 week
|
GRoC is a reliable assessment method with 11 levels, frequently used to track changes in a participant's condition.
Participants who selected the top two categories (much better and very much better) were considered recovered.
|
Baseline and at 6 week
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 09/972
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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