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

Status

Completed

Conditions

Intervention / Treatment

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
      • 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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