Impact of a Cueing Device on Upper Extremity Muscle Strength in Swimmers

April 7, 2026 updated by: Kevin Strehler, University of South Alabama

Impact of a Cueing Device on Upper Extremity Muscle Strength in Swimmers: A 6-Week Training Protocol Using Scapular Stabilization Exercises.

The goal of this study is to find out if a tool called an external cueing device (ECD) can help young swimmers improve their shoulder function. An ECD is a tool that limits arm movement and gives the swimmer a target to focus on while doing exercises. The main questions this study will answer are:

  • Does using an ECD during certain exercises improve muscle strength?
  • Does using an ECD while exercising help with shoulder stability?

Participants will:

  • Test their shoulder muscle strength and stability at the beginning of the study.
  • Complete 8 exercises as part of their regular dry-land training program for 6 weeks.
  • Repeat the same tests after 3 weeks and again at the end of the study.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

36

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

    • Alabama
      • Mobile, Alabama, United States, 36603
        • Fredericka G. Evans Cultural Centre

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

  • Child
  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Healthy Volunteer Adolescent Swimmers
  • Member of CMSA

Exclusion Criteria:

  • Swimmers under the age of 11 years of age.
  • Swimmers that are not registered as athletes through United States Swimming.
  • Swimmers that are not enrolled in Age Group III, Senior 1, Senior 2, or Senior 3
  • Swimmers not attending practice due to an injury (i.e., shoulder, back, etc.).
  • Swimmers currently not participating in a dryland program offered through CMSA.

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Shoulder Stabilization Exercise
Protocol contains 8 exercises ("I", "Y", "T", "i", "w", alternating arm "I"/"i", "n", and supine serratus punch) completed for 8 repetitions each for 3 weeks, and in weeks 4-6 completed at 2 sets of 8 repetitions each. Standard group coaching assistance will be provided.
Shoulder stabilization exercise protocol contains 8 exercises ("I", "Y", "T", "i", "w", alternating arm "I"/"i", "n", and supine serratus punch) completed for 8 repetitions each for 3 weeks, and in weeks 4-6 completed at 2 sets of 8 repetitions each.
Experimental: Shoulder Stabilization Exercise with External Cueing Device
Protocol contains 8 exercises ("I", "Y", "T", "i", "w", alternating arm "I"/"i", "n", and supine serratus punch) completed for 8 repetitions each for 3 weeks, and in weeks 4-6 completed at 2 sets of 8 repetitions each. External cueing device provides movement pattern constraint and an external target zone for the individual for each exercise. Standard group coaching assistance will be provided.
Shoulder stabilization exercise protocol contains 8 exercises ("I", "Y", "T", "i", "w", alternating arm "I"/"i", "n", and supine serratus punch) completed for 8 repetitions each for 3 weeks, and in weeks 4-6 completed at 2 sets of 8 repetitions each.
A portable product that provides movement pattern constraints to ensure improved exercise form, and provides a target zone for exercise effort

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline in isometric muscle torque production at 180 degrees shoulder abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Handheld dynamometer assessment of force production times lever arm distance (Newton.meters) of prone shoulder elevation in 180 degrees of abduction completed at baseline, after 3 and 6 weeks of the training program.
Baseline, 3 weeks, 6 weeks.
Change from baseline in isometric muscle torque production at 135 degrees shoulder abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Handheld dynamometer assessment of force production times lever arm distance (Newton.meters) of prone shoulder elevation in 135 degrees of abduction completed at baseline, after 3 and 6 weeks of the training program.
Baseline, 3 weeks, 6 weeks.
Change from baseline in isometric muscle torque production at 90 degrees shoulder abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Handheld dynamometer assessment of force production times lever arm distance (Newton.meters) of prone shoulder elevation in 90 degrees of abduction completed at baseline, after 3 and 6 weeks of the training program.
Baseline, 3 weeks, 6 weeks.
Change from baseline in modified Athletic Shoulder Test at 180 degrees shoulder abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Maximum isometric force production with lying prone into a handheld dynamometer at a given lever arm distance results in muscle torque (Newton.meters) reading. This portion of the test is conducted at 180 degrees of abduction.
Baseline, 3 weeks, 6 weeks.
Change from baseline in modified Athletic Shoulder Test at 135 degrees shoulder abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Maximum isometric force production with lying prone into a handheld dynamometer at a given lever arm distance results in muscle torque (Newton.meters) reading. This portion of the test is conducted at 135 degrees of abduction.
Baseline, 3 weeks, 6 weeks.
Change from baseline in modified Athletic Shoulder Test at 90 degrees shoulder abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Maximum isometric force production with lying prone into a handheld dynamometer at a given lever arm distance results in muscle torque (Newton.meters) reading. This portion of the test is conducted at 90 degrees of abduction.
Baseline, 3 weeks, 6 weeks.
Closed Kinetic Chain Upper Extremity Stability Test Power Score
Time Frame: Baseline, 6 weeks.
Two strips of tape are placed 36 inches apart. Participants assume a push up position (male) or pushup on knees (Female) and are instructed to reach across and touch the opposing hand alternating arms. Maximum number of touches in 15 seconds is recorded. Normalization is made by multiplying the raw touch score by 0.68 x Subject weight in Kg (representing the mass on the head arms and trunk) and dividing by the 15 seconds. Higher number indicates increased shoulder stability.
Baseline, 6 weeks.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Closed Kinetic Chain Upper Extremity Stability Test Raw Touch Score
Time Frame: Baseline, 6 weeks.
Two strips of tape are placed 36 inches apart. Participants assume a push up position (male) or pushup on knees (Female) and are instructed to reach across and touch the opposing hand alternating arms. Maximum number of touches in 15 seconds is recorded. Higher number of touches indicates increased shoulder stability
Baseline, 6 weeks.
Closed Kinetic Chain Upper Extremity Stability Test Touch Score
Time Frame: Baseline, 6 weeks.
Two strips of tape are placed 36 inches apart. Participants assume a push up position (male) or pushup on knees (Female) and are instructed to reach across and touch the opposing hand alternating arms. Maximum number of touches in 15 seconds is recorded. Touches are adjusted for subject height by dividing raw touch by subject height (in inches based on prior literature). Higher number of touches indicates increased shoulder stability
Baseline, 6 weeks.
Maximal Prone Arm Elevation at 180 degrees abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Distance from floor to wrist crease, measured in cm.
Baseline, 3 weeks, 6 weeks.
Maximal Prone Arm Elevation at 135 degrees abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Distance from floor to wrist crease, measured in cm.
Baseline, 3 weeks, 6 weeks.
Maximal Prone Arm Elevation at 90 degrees abduction
Time Frame: Baseline, 3 weeks, 6 weeks.
Distance from floor to wrist crease, measured in cm.
Baseline, 3 weeks, 6 weeks.

Collaborators and Investigators

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

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)

April 20, 2025

Primary Completion (Actual)

July 25, 2025

Study Completion (Actual)

July 25, 2025

Study Registration Dates

First Submitted

March 29, 2025

First Submitted That Met QC Criteria

April 4, 2025

First Posted (Actual)

April 11, 2025

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 7, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

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

product manufactured in and exported from the U.S.

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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