- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06070909
Selective Activation of the Infraspinatus During External Rotation Exercises in Participants With Rounded Shoulder Posture
October 1, 2023 updated by: Ankara Yildirim Beyazıt University
Selective Activation of the Infraspinatus During External Rotation Exercises in Participants With Rounded Shoulder Posture: Comparison of 3 Common Exercises and Muscle Architecture-Based Exercise
The purpose of this prospective, cross-sectional study was to evaluate the selective activation of the infraspinatus during external rotation exercises in participants with rounded shoulder postures and compare the different exercise positions.
The fifteen (7 males and 8 females) participants with rounded shoulder posture were recruited for this study.
The EMG activations of the middle trapezius, posterior deltoid and infraspinatus muscles in the dominant limb were recorded during exercises in standing external rotation (SER), side-lying position (SDER), scapular plane (SPER) and muscle architecture-based (MABER) positions.
Study Overview
Study Type
Observational
Enrollment (Actual)
15
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Etlik
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Ankara, Etlik, Turkey, 06010
- Ankara Yıldırım Beyazıt University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation
-
-
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
Yes
Sampling Method
Probability Sample
Study Population
Fifteen (7 males and 8 females) participants without shoulder pain, totally able to perform overhead activities with no pain or discomfort, without a history of shoulder injuries, and with rounded shoulder posture were recruited for this study.
Description
Inclusion Criteria:
- without shoulder pain,
- totally able to perform overhead activities with no pain or discomfort,
- without a history of shoulder injuries
- with rounded shoulder posture
Exclusion Criteria:
- a history of shoulder muscle injury
- bone fractures in shoulder region
- luxation or subluxation
- cervical dysfunction radiating to upper limbs
- neurologic or musculoskeletal disorders that would prevent shoulder external rotation in the testing postures.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The EMG activations of the middle trapezius, posterior deltoid and infraspinatus muscles in the dominant limb
Time Frame: 4 weeks
|
The EMG activations of the middle trapezius, posterior deltoid and infraspinatus muscles in the dominant limb were recorded during exercises in standing external rotation (SER), side-lying position (SDER), scapular plane (SPER) and muscle architecture-based (MABER) positions
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
July 15, 2023
Primary Completion (Actual)
July 20, 2023
Study Completion (Actual)
July 30, 2023
Study Registration Dates
First Submitted
October 1, 2023
First Submitted That Met QC Criteria
October 1, 2023
First Posted (Actual)
October 6, 2023
Study Record Updates
Last Update Posted (Actual)
October 6, 2023
Last Update Submitted That Met QC Criteria
October 1, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 38b5558f4bdd45f8
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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