Is There an Immediate Effect on Pectoralis Minor Length After Performing a Prone Scapular Retraction Exercise

April 2, 2024 updated by: Andrews University

Is There an Immediate Effect on Pectoralis Minor Length After Performing a Prone Scapular Retraction Exercise Using Typical Sets and Repetitions in Pain Free Participants

The goal of this clinical trial is to test normal participants.

The main question it aims to answer is:

• Do the participant's pectoralis minor muscles change length immediately after performing an exercise that recruits the scapular retractor muscles? Participants will have their pectoralis minor muscle measured, then perform an exercise recruiting the scapular retractor muscles, and then have their pectoralis muscle measured again.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The participants will have their standing height measured in centimeters with a tape measure fixed against a wall. Participants will then step away from the wall and will be asked to stand in their normal resting position. A mark will be placed on the most medial-inferior aspect of the coracoid process and a second mark on the anterior-inferior edge of the third rib, one index finger's width lateral to the sternum. A caliper will then be used to measure the distance between these marks as the participant holds a normal exhalation.

Participants will then lay prone on a treatment plinth with a small towel roll under their forehead. The participants will form both fists and place them on the plinth just superior to their head, with bilateral thumbs up and the ulnar side of the hands resting on the plinth, and their arms relaxed so their elbows remain on the plinth. The participants will then lift their elbows off the plinth as high as possible while keeping their hands on the plinth. The participants will repeat this motion for 10 repetitions, performing three sets of this exercise with 30 seconds of rest in between each set.

After the third set, the participants will stand up and a second caliper will be used to once again measure PM length by the same tester using the same marks. This will conclude the testing procedure and the participant's involvement in the study.

Study Type

Interventional

Enrollment (Actual)

50

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 Locations

    • Idaho
      • Hayden, Idaho, United States, 83835
        • North Idaho Physical Therapy

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18 years of age or older. At least 130 degrees of shoulder elevation. None of the exclusion criteria.

Exclusion Criteria:

  • Current shoulder pathology and or pain, prior shoulder surgery, any neurological impairment, any upper quarter deformity, a fracture of the upper extremity, or systemic inflammatory disease.

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention arm
Participants who underwent intervention.
Participant lies prone with hands superior to the head on a treatment plinth and lifts their elbows 10 repetitions for three sets with 30 seconds of rest between each set.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pectoralis Minor Length
Time Frame: Measured before and immediately after intervention
Length of the Pectoralis Muscle length in millimeters
Measured before and immediately after intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jeremy Dye, MPT, North Idaho Physical Therapy

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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, 2021

Primary Completion (Actual)

January 10, 2022

Study Completion (Actual)

January 10, 2022

Study Registration Dates

First Submitted

February 28, 2024

First Submitted That Met QC Criteria

April 2, 2024

First Posted (Actual)

April 4, 2024

Study Record Updates

Last Update Posted (Actual)

April 4, 2024

Last Update Submitted That Met QC Criteria

April 2, 2024

Last Verified

November 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 12241976

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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