- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06923930
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
Conditions
Intervention / Treatment
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.
Sponsor
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.
General Publications
- de Oliveira VM, Pitangui AC, Nascimento VY, da Silva HA, Dos Passos MH, de Araujo RC. TEST-RETEST RELIABILITY OF THE CLOSED KINETIC CHAIN UPPER EXTREMITY STABILITY TEST (CKCUEST) IN ADOLESCENTS: RELIABILITY OF CKCUEST IN ADOLESCENTS. Int J Sports Phys Ther. 2017 Feb;12(1):125-132.
- Tooth C, Forthomme B, Croisier JL, Gofflot A, Bornheim S, Schwartz C. The Modified-Athletic Shoulder Test: Reliability and validity of a new on-field assessment tool. Phys Ther Sport. 2022 Nov;58:8-15. doi: 10.1016/j.ptsp.2022.08.003. Epub 2022 Aug 30.
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2305310-1/2304240-1
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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