- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06552585
Effect of Two Preventive Exercise Programs for Swimmer's Shoulder on the Torque of Shoulder Rotator Muscles in Competitive Swimmers
August 10, 2024 updated by: Nuno Tavares, School of Allied Health Sciences of Porto (ESTSP) - Polytechnic Institute of Porto (IPP)
Effect of Two Preventive Exercise Programs for Swimmer's Shoulder on the Torque of Shoulder Rotator Muscles in Competitive Swimmers: a Randomized Controlled Trial
The purpose of this study was to verify the effectiveness of two 12-week preventive exercise programs for swimmer's shoulder with monitoring and progression over time, on the peak torque and respective conventional concentric ratio and functional ratio.
One of these programs was performed with weights and the other with an elastic band.
This study hypothesized that the two preventive exercise programs minimize shoulder rotators imbalanced during the swimming season.
The study design is a care provider and participants blinded, parallel, randomized controlled trial
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
30
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
-
-
-
Coimbra, Portugal, 3045-093
- Instituto Politécnico de Coimbra - RoboCorp
-
-
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
Yes
Description
Inclusion Criteria:
- Competitve swimmer in the current season.
- Aged between 16-35 years old.
- Have a minimum of 5 years of experience in national competitions.
- Performed a minimum of 8 hours of weekly swimming training.
Exclusion Criteria:
- Subjects who had performed at least 6 weeks of treatment such as physical therapy, injections, and medication.
- Clinical situations such as a history of significant shoulder pain in the last 6 months, a history of traumatic shoulder injuries such as fractures, subluxations, cervical or thoracic conditions, previous shoulder surgeries, shoulder range of motion deficits, or neurological injuries.
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Sham Comparator: Control
|
The control group performed a sham intervention, twice a week, for 12-weeks.
This intervention consisted of 2 sets of 10 repetitions of 5 shoulder mobility exercises, without preventive aim, normally carried out in warm-up before training: shoulder maximum flexion and extension, horizontal abduction and adduction starting from 90º of shoulder abduction, maximum internal/external rotation starting from 90º of shoulder abduction, circumduction of the shoulder in a clockwise direction and circumduction of the shoulder in a counterclockwise direction.
There was no progression after 6-weeks of this sham intervention.
The coach of the respective team checked the execution of the exercises, but there was no individualized monitoring with a regular exercise technique correction by a physiotherapist.
|
|
Experimental: Weight program group
|
Twice a week, over 12-weeks, the weight program group carried out a strength program with the 5 open kinetic chain exercises most often reported in the literature to prevent swimmer's shoulder - internal rotation at 90°, external rotation at 90°, scapular punches, T's, and Y's - with two weights Domyos with 1, 2, 3, 4, or 5 kg.The load used to perform the programs with weights were previously assessed and adjusted for each swimmer, corresponding to 75% of one repetition maximum.
After 6 weeks of program execution, each swimmer carried out another one repetition maximum test assessment, to verify the possibility of a load instrument progression.
|
|
Experimental: Elastic band program group
|
Twice a week, over 12-weeks, the elastic band program group carried out a strength program with the 5 open kinetic chain exercises most often reported in the literature to prevent swimmer's shoulder - internal rotation at 90°, external rotation at 90°, scapular punches, T's, and Y's - with an elastic band Bodytone Power Band with 10, 15, 20, 25, or 30 kg weights Domyos.The load used to perform the programs with weights were previously assessed and adjusted for each swimmer, corresponding to 75% of one repetition maximum.
After 6 weeks of program execution, each swimmer carried out another one repetition maximum test assessment, to verify the possibility of a load instrument progression.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peak torque
Time Frame: 12 weeks
|
The concentric and eccentric peak torque of internal and external rotators of the dominant and non-dominant shoulders at 60°/s, 120°/s and 180°/s, evaluated through an isokinetic dynamometer Biodex System 3 (Biodex Medical Systems, New York).
|
12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Conventional concentric external/internal shoulder rotators ratio
Time Frame: 12 weeks
|
The quotient between peak torque values of the concentric external and internal rotators of the shoulder multiplied by 100.
|
12 weeks
|
|
Functional eccentric external/concentric internal shoulder rotators ratio
Time Frame: 12 weeks
|
The quotient between peak torque values of the eccentric external rotators of the shoulder and concentric internal rotators of the shoulder multiplied by 100.
|
12 weeks
|
|
Time to peak torque
Time Frame: 12 weeks
|
The time between the beginning of the torque caption and the peak torque previously described.
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Maria António Castro, PhD, Instituto Politécnico de Leiria
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)
September 1, 2022
Primary Completion (Actual)
November 1, 2022
Study Completion (Actual)
April 30, 2023
Study Registration Dates
First Submitted
August 7, 2024
First Submitted That Met QC Criteria
August 10, 2024
First Posted (Actual)
August 14, 2024
Study Record Updates
Last Update Posted (Actual)
August 14, 2024
Last Update Submitted That Met QC Criteria
August 10, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SchoolAHSP
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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