- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07554248
Effects of Low-Intensity Technical Tethered Swimming on Front Crawl Kinematics in Adolescent Swimmers
April 23, 2026 updated by: Józef Piłsudski University of Physical Education
Effect of Low-Intensity Technical Tethered Swimming Training on Front Crawl Kinematics in Adolescent Swimmers
This study evaluated the acute effects of two low-intensity front crawl training conditions on swimming kinematics in adolescent swimmers.
After a standardized warm-up, participants performed either low-intensity tethered front crawl or low-intensity free-swimming front crawl.
Kinematic measurements were obtained immediately after task completion using an accelerometer.
One week later, the final exercise condition was rotated between groups so that both groups completed both training conditions.
Study Overview
Status
Completed
Detailed Description
This study investigated the effects of two low-intensity front crawl training conditions on swimming kinematics in adolescent swimmers.
All participants completed the same standardized warm-up protocol.
After the warm-up, Group A performed 6 × 10 cycles of low-intensity tethered front crawl with 10-second rest intervals between sets, while Group B performed 6 × 50 m of low-intensity front crawl starting every 60 seconds.
During both exercise conditions, participants were instructed to focus on stroke length and correct body position in the water.
Study Type
Interventional
Enrollment (Actual)
32
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
-
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Masovian Voivodeship
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Warsaw, Masovian Voivodeship, Poland, 02-785
- Swimming Pool at Koncertowa 4
-
-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Competitive adolescent swimmers from a local sports club
- Regular swimming training history since approximately 9-10 years of age
- Current training frequency of approximately 7-8 sessions per week
- Regular participation in national-level swimming competitions
- At least 2 years of regular swimming training experience
- Ability to complete the study procedures, including low-intensity front crawl conditions and accelerometer-based measurement
Exclusion Criteria:
- Current injury or musculoskeletal condition preventing participation
- Failure to meet the required age criteria
- Less than 2 years of regular swimming training experience
- Inability to complete the study procedures
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: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Sequence A
Participants completed low-intensity tethered front crawl in the first session and low-intensity free front crawl in the second session, one week later.
|
Participants performed 6 × 10 cycles of low-intensity front crawl while tethered, with 10-second rest intervals between sets.
During the exercise, participants were instructed to focus on stroke length and correct body position in the water.
Participants performed 6 × 50 m of low-intensity front crawl, starting every 60 seconds.
During the exercise, participants were instructed to focus on stroke length and correct body position in the water.
|
|
Experimental: Sequence B
Participants completed low-intensity free front crawl in the first session and low-intensity tethered front crawl in the second session, one week later.
|
Participants performed 6 × 10 cycles of low-intensity front crawl while tethered, with 10-second rest intervals between sets.
During the exercise, participants were instructed to focus on stroke length and correct body position in the water.
Participants performed 6 × 50 m of low-intensity front crawl, starting every 60 seconds.
During the exercise, participants were instructed to focus on stroke length and correct body position in the water.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Front Crawl Kinematic Variables Measured by Accelerometer
Time Frame: Baseline and 1 week
|
ront crawl kinematic variables were assessed with an accelerometer during each 50 m front crawl trial performed after the assigned exercise condition.
Variables included body roll (maximum angular velocity around the vertical axis [ωmaxR] and maximum pelvic tilt angle around the vertical axis [AmaxR]), yaw rotation (maximum angular velocity around the sagittal axis [ωmaxY] and acceleration along the transverse axis [atmax]), pitch rotation (maximum angular velocity around the transverse axis [ωmaxP] and acceleration along the sagittal axis [asmax]), and progressive movement (maximum acceleration along the vertical axis [avmax]).
|
Baseline and 1 week
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time to Achieve 50 m
Time Frame: Baseline and 1 week
|
Time required to complete 50 m front crawl, expressed in seconds.
|
Baseline and 1 week
|
|
Stroke Length
Time Frame: Baseline and 1 week
|
Stroke length during front crawl, expressed in meters.
|
Baseline and 1 week
|
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)
June 14, 2024
Primary Completion (Actual)
June 21, 2024
Study Completion (Actual)
June 21, 2024
Study Registration Dates
First Submitted
April 17, 2026
First Submitted That Met QC Criteria
April 23, 2026
First Posted (Actual)
April 28, 2026
Study Record Updates
Last Update Posted (Actual)
April 28, 2026
Last Update Submitted That Met QC Criteria
April 23, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- SKE 01-31/2023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be shared.
Processed and aggregated research data used for analysis may be shared separately in a public repository.
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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