- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07691723
Low-Volume High-Intensity Race-Pace Training in Finswimmers (LVHI-FS-TdeA)
Individual Responses to a Low-Volume, High-Intensity Race-Pace Training Block in Finswimmers From the Antioquia Underwater Activities League: A Prospective Single-Group Case Series
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Finswimming is a high-speed aquatic sport in which performance in short and middle-distance events depends on the ability to produce and sustain race-specific velocity. Traditional aquatic training models often emphasise high training volume; however, for events lasting from seconds to a few minutes, race-pace work, neuromuscular quality, and individualised load monitoring may be particularly relevant.
This study will prospectively follow approximately seven finswimmers from the Antioquia Underwater Activities League (LASA) during a 9-week low-volume, high-intensity training block. All participants will receive the same general training approach, but training distances, repetitions, target times, and race-pace references will be individualised according to each athlete's main competitive event.
Before the intervention, athletes will complete a basic characterisation and a baseline performance assessment using either an official competition result or a standardised control test. Training target times will be estimated from the baseline performance. During the 9-week block, the investigators will record external load variables, including distance, repetitions, weekly volume, target time, and actual time for each relevant repetition. Internal load will be monitored using heart rate and rating of perceived exertion. Pace stability will be estimated from repeated times in event-specific distances using descriptive indicators such as mean time, standard deviation, and coefficient of variation.
After the intervention, performance will be reassessed in the athlete's main event through an official competition or a comparable standardised control test. Data analysis will focus on individual responses, weekly trends, and descriptive changes from baseline to post-intervention. The study will not include a control group or randomisation; therefore, findings will be interpreted as exploratory and non-causal.
Study Type
Enrollment (Estimated)
Phase
- Early Phase 1
Contacts and Locations
Study Contact
- Name: Samuel Jose Gaviria Alzate, PhD
- Phone Number: +573192772912
- Email: samuel.gaviria@tdea.edu.co
Study Locations
-
-
Antioquia
-
Guarne, Antioquia, Colombia, 054080
- Tecnológico de Antioquia
-
Contact:
- Samuel Jose Gaviria Alzate, PhD
- Phone Number: 00573192772912
- Email: samuel.gaviria@tdea.edu.co
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Finswimmers affiliated with the Antioquia Underwater Activities League (LASA).
- Regular participation in finswimming training.
- A defined main competitive event.
- Availability to complete the 9-week follow-up period.
- Ability to complete high-intensity swimming training according to the regular sport programme.
- Written informed consent from adult participants.
- For participants under 18 years of age, written informed consent from a parent or legal guardian and written assent from the participant.
Exclusion Criteria:
- Active musculoskeletal injury.
- Relevant pain or acute illness at baseline.
- Medical restriction for high-intensity swimming exercise.
- Inability to complete the planned follow-up.
- Withdrawal of consent or assent.
- Insufficient attendance or incomplete records for the main study variables.
- Any condition judged by the research team or coaching staff to compromise participant safety during high-intensity swimming.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Low-volume high-intensity race-pace finswimming training
Participants will complete a 9-week finswimming training block focused on low-volume, high-intensity, race-pace swimming.
Training will be individualised according to each athlete's main competitive event and monitored using external load, heart rate, rating of perceived exertion, and repetition times.
|
The intervention will consist of a 9-week finswimming training block oriented towards race-specific pace.
Participants will perform repeated swimming efforts prescribed according to individual target times derived from baseline performance.
Training sessions will include event-specific distances, repetitions, recovery periods, and target intensities.
External load will be monitored through distance, repetitions, weekly volume, target time, and actual time.
Internal load will be monitored using heart rate and rating of perceived exertion.
Training volume will be adjusted according to the athlete's event profile and reduced towards the final phase when tapering is required.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in main-event finswimming performance time
Time Frame: Baseline and week 9
|
Performance time, in seconds, will be recorded for each participant's main competitive event.
The baseline value will be obtained from an official competition result or a standardised control test before the training block.
The post-intervention value will be obtained from an official competition result or a comparable standardised control test after the 9-week block.
A lower time will indicate better performance.
|
Baseline and week 9
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline in mean swimming velocity
Time Frame: Baseline and week 9
|
Mean swimming velocity will be calculated from the performance distance and time in each participant's main event.
Velocity will be expressed in metres per second.
A higher value will indicate better performance.
|
Baseline and week 9
|
|
Weekly external training volume
Time Frame: Weekly from baseline to week 9
|
External training volume will be quantified as the total metres completed per week during recorded race-pace or event-specific swimming repetitions.
|
Weekly from baseline to week 9
|
|
Weekly mean heart rate during recorded swimming repetitions
Time Frame: Weekly from baseline to week 9
|
Heart rate will be recorded during training sessions using a heart rate monitor, sport watch, or equivalent device.
Weekly mean heart rate will be reported in beats per minute.
|
Weekly from baseline to week 9
|
|
Weekly rating of perceived exertion
Time Frame: Weekly from baseline to week 9
|
Rating of perceived exertion will be recorded using a numerical perceived exertion scale after relevant sets or at the end of the session, according to the predefined monitoring protocol.
Weekly mean values will be described for each participant.
|
Weekly from baseline to week 9
|
|
Pace stability during event-specific swimming repetitions
Time Frame: Repeated training sessions from baseline to week 9
|
Pace stability will be estimated from repeated swimming times in event-specific distances.
The coefficient of variation will be calculated for each participant and distance when repeated measurements are available.
Lower values will indicate greater pace stability.
|
Repeated training sessions from baseline to week 9
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- LVHI-Finswimmers-TdeA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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