- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06202391
Autogenic Inhibition Versus Reciprocal Inhibition Muscle Energy Techniques Effect on Swimming Performance on Swimmers With Scapular Dyskinesis
January 1, 2024 updated by: Foundation University Islamabad
Swimming can cause shoulder pain due to scapular dyskinesis.
Proper scapula movement is necessary for efficient swimming strokes and to avoid injury.
Studying the effects of autogenic and reciprocal inhibition muscle energy techniques on swimmers with scapular dyskinesis can lead to effective interventions and reduce shoulder injuries
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Efficient swimming strokes require proper positioning of the scapula.
Scapular dyskinesis (SD) is a condition where normal scapular kinematics are altered due to injury or changes in muscle activation.
Swimmers, who are considered overhead athletes, have risk of developing SD.
Even individuals who do not experience symptoms can have SD, and it may lead to future shoulder injuries.
Early diagnosis and treatment of this condition can prevent it from progressing and minimize the risk of injury.
Additionally, using autogenic and reciprocal inhibition muscle energy techniques can enhance the activation of the appropriate muscles responsible for scapular movement, which can lead to more effective interventions, improved swimming performance, and reduced injury risk. he intervention protocol (Muscle energy techniques to the upper fibers of the Trapezius, Levator Scapulae, Pectoralis Major, Latissimus Dorsi) will be conducted for 8-14 minutes over 3 weeks with 12 sessions/4 times a week.
Outcomes measure will be assessed after the intervention period and data will be analyzed.
Study Type
Interventional
Enrollment (Estimated)
34
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 Contact
- Name: Ayesha Sameen, MS-MSKPT*
- Phone Number: 03394016858
- Email: ayessha.sameen@gmail.com
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Recruiting
- Foundation University College of Physical Therapy
-
Contact:
- Sana Bashir, DPT, MS-CPPT,PHD*
- Phone Number: 03218529475
- Email: Sana.bashir65@gmail.com
-
-
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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Swimmers with at least four times training per week
- Does not have any shoulder pain or injury or operation to the shoulders
- Positive Scapular Dyskinesis diagnosis test
- Freestyle (also known as a front crawl) swimming stroke
Exclusion criteria:
- Shoulder pain in the last six months
- History of shoulder surgery or fracture within the last six months
- Frequent practice of physical activity in any other sport
- Negative result of the Scapular Dyskinesis test
- Other swimming strokes
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 |
---|---|
Experimental: Group A (Autogenic inhibition muscle energy technique)
12 sessions will be conducted over a period of 4 weeks with 3 days per week Frequency: 12 sessions, four times a week for 3 consecutive weeks Time duration: apporx.
8 to 10 minutes
|
Autogenic Inhibition-MET protocol: 3-5 repetitions of post isometric relaxation (PIR) (30- 50% isometric contraction of the muscle to be stretched for 5-10 seconds, followed by rest period of 5 seconds and then a stretch of 20-30 seconds' hold.
A total of 12 sessions, four times a week, for three consecutive weeks.
|
Experimental: Group B (Reciprocal inhibition muscle energy technique)
12 sessions will be conducted over a period of 3 weeks with 4 days per week Frequency: 12 sessions, four times a week for 3 consecutive weeks Time duration: apporx. 8 to 10 minutes |
Reciprocal Inhibition-MET protocol: 3-5 repetitions of Reciprocal Inhibition (RI) MET (30- 50% isometric contraction of the muscle opposite to the muscle to be stretched for 5-10 seconds, followed by rest period of 5 seconds and then a stretch of 20-30 seconds' hold A total of 12 sessions, four times a week, for three consecutive weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stroke velocity
Time Frame: 3 weeks
|
Stroke velocity will be assessed using KINOVEA
|
3 weeks
|
Stroke rate
Time Frame: 3 weeks
|
Stroke rate will be assessed using KINOVEA
|
3 weeks
|
stroke length
Time Frame: 3 weeks
|
Stroke length will be assessed using KINOVEA
|
3 weeks
|
Total strokes
Time Frame: 03 Week
|
Total strokes will be assessed using KINOVEA
|
03 Week
|
Stroke time
Time Frame: 03 Week
|
Stroke time will be assessed using KINOVEA
|
03 Week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
August 30, 2023
Primary Completion (Estimated)
January 15, 2024
Study Completion (Estimated)
February 1, 2024
Study Registration Dates
First Submitted
January 1, 2024
First Submitted That Met QC Criteria
January 1, 2024
First Posted (Estimated)
January 11, 2024
Study Record Updates
Last Update Posted (Estimated)
January 11, 2024
Last Update Submitted That Met QC Criteria
January 1, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2023/27
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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