ClinicalTrials.gg
CompletedNCT07862036Updated Oct 7, 2026

HIIT Versus High-Volume Training in Competitive Para Swimmers

An interventional study of Reduced-Volume High-Intensity Interval Swimming Training and Higher-Volume Moderate-Intensity Swimming Training in Physical Disability, Intellectual Impairment and Athletic Performance, sponsored by National and Kapodistrian University of Athens. Completed at 1 site in Greece. Open to participants aged 12 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-07.

Sponsored by National and Kapodistrian University of Athens · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 4 years after the study started (first participant enrolled Sep 2022, registered Sep 2026).
Updated Oct 7, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
12 Years and older
Sex
All
01

Study summary

This study compared the effects of four weeks of reduced-volume high-intensity interval training and higher-volume moderate-intensity swimming training on repeated-sprint ability, physiological responses, and body composition in competitive para swimmers. Twenty-four national-level swimmers representing World Para Swimming sport classes S5-S10 and S14 were randomly allocated to one of the two training interventions by drawing sealed group assignments. Both groups completed two supervised sessions per week for four weeks. Repeated-sprint ability was assessed before and after the intervention using eight maximal 15-m freestyle sprints.

Read the detailed description

Competitive para swimmers with physical or intellectual impairments were purposively recruited to provide representation across the included World Para Swimming sport classes. After enrollment and baseline assessment, participants were randomly allocated to reduced-volume high-intensity interval training or higher-volume moderate-intensity training by drawing sealed group assignments. The study used a two-arm, randomized, parallel-group, active-comparator design.

Both interventions lasted four weeks and included two supervised swimming sessions per week. The high-intensity intervention used lower-volume maximal and near-maximal swimming efforts, whereas the active-comparator intervention used a higher volume of moderate-intensity swimming.

Repeated-sprint ability was evaluated using eight maximal 15-m freestyle sprints separated by a standardized 30-s interval. The interval began when the swimmer crossed the 15-m timing marker and included a controlled low-intensity 6-m return to the wall followed by stationary in-water recovery. Repeated-sprint outcomes included ideal sprint time, total sprint time, and performance decrement. Physiological responses and body-composition measures were also obtained before and after the training intervention.

02

Conditions studied

  • Physical Disability
  • Intellectual Impairment
  • Athletic Performance
  • Exercise Training

Keywords

  • para swimming
  • para swimmers
  • Repeated-sprint ability
  • High-intensity interval training
  • HIIT
  • High-volume training
  • Swimming performance
  • Disability sport
  • Exercise training
  • Performance decrement
03

In context

Lead sponsor

National and Kapodistrian University of Athens is the lead sponsor of 172 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Classified in Para Swimming sport class S5, S6, S7, S8, S9, S10, or S14. At least 12 years of age. Active competitive swimmer participating at the national level. Had won at least one national championship medal during the preceding two competitive seasons.

Regularly participating in organized swimming training. Able to understand and complete the adapted repeated-sprint swimming protocol. Provided written informed consent; for minors, consent was provided by a parent or legal guardian, and assent was obtained where applicable.

Exclusion criteria

Exclusion Criteria:

Medical contraindication to maximal-intensity swimming exercise. Acute illness or injury preventing participation in testing or training. Change in medication or health status expected to influence exercise responses. Failure to complete the required familiarization, baseline testing, or intervention sessions.

Participation in another intervention likely to affect the study outcomes.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
24 participants (actual)

Study arms

  • Experimental
    Reduced-Volume High-Intensity Interval Training

    Participants completed two supervised sessions per week for four weeks. The main training sets incorporated high-intensity or maximal swimming efforts and had approximately 50% less training volume than the main sets completed by the higher-volume group.

    Behavioral: Reduced-Volume High-Intensity Interval Swimming Training

  • Other
    Higher-Volume Moderate-Intensity Swimming Training

    The active-comparator intervention lasted four weeks and included two supervised sessions per week. Participants completed 50-, 100-, and 200-m freestyle intervals at moderate intensity using the predefined work-to-recovery structure. Intensity was monitored using heart rate and rating of perceived exertion, targeting approximately 60%-75% of estimated maximum heart rate and ratings of 3-4 on the Borg CR10 scale. Main-set volume was approximately 50% greater than in the high-intensity intervention.

    Behavioral: Higher-Volume Moderate-Intensity Swimming Training

Interventions

  • BehavioralReduced-Volume High-Intensity Interval Swimming Training

    The intervention lasted four weeks and included two supervised sessions per week. Main-set activities included intermittent 50-m swims with short recovery intervals, 25-m all-out sprints using a 1:1 work-to-recovery ratio, and five 30-s tethered maximal efforts with 2 min 30 s of recovery between efforts. The precise session content progressed according to the predefined training schedule.

  • BehavioralHigher-Volume Moderate-Intensity Swimming Training

    The active-comparator intervention lasted four weeks and included two supervised sessions per week. Participants completed 50-, 100-, and 200-m freestyle intervals at moderate intensity using the predefined work-to-recovery structure. Intensity was monitored using heart rate and rating of perceived exertion, targeting approximately 60%-75% of estimated maximum heart rate and moderate intensity ratings (e.g., 3-4) on the Borg CR10 scale. Main-set volume was approximately 50% greater than in the high-intensity intervention.

06

What researchers measure

Primary outcomes

  1. Change in Total Sprint Time

    Total sprint time, measured in seconds, was calculated as the sum of the eight 15-m maximal freestyle sprint times. Lower values indicate better overall repeated-sprint performance.

    Time frame: Baseline and two days after the final training session at four weeks

  2. Change in Ideal Sprint Time

    Ideal sprint time, measured in seconds, was calculated as the fastest single 15-m sprint time multiplied by eight. Lower values indicate better performance.

    Time frame: Βaseline and two days after the final training session at four weeks

  3. Change in Performance Decrement

    Performance decrement was calculated as \[(total sprint time / ideal sprint time) × 100\] - 100 and expressed as a percentage. Lower values indicate less performance loss across the eight sprint repetitions

    Time frame: Βaseline and two days after the final training session at four weeks

  4. Change in 50-m and 200-m Freestyle Performance

    Swimming performance is evaluated by the time (in seconds) required to complete 50-m and 200-m maximal freestyle tests. Lower values indicate better performance.

    Time frame: Baseline and two days after the final training session at four weeks

  5. Change in Stroke Rate

    Stroke Rate (cycles/min) was assessed via video analysis during the swimming efforts.

    Time frame: Baseline and two days after the final training session at four weeks

  6. Changes in Stroke Length

    Stroke Length (m/cycle) was assessed via video analysis during the swimming efforts.

    Time frame: Βaseline and two days after the final training session at four weeks

  7. Change in heart rate

    Physiological markers were assessed pre- and post-exercise, including heart rate (beats/min).

    Time frame: Baseline and two days after the final training session at four weeks

  8. Change in blood lactate concentration

    Physiological markers were assessed pre- and post-exercise, including blood lactate concentration (mmol/L).

    Time frame: Βaseline and two days after the final training session at four weeks

  9. Change in oxygen saturation

    Physiological markers were assessed pre- and post-exercise, including oxygen saturation (%).

    Time frame: Βaseline and two days after the final training session at four weeks

  10. Change in fatigue index

    Physiological markers were assessed pre- and post-exercise, including the fatigue index.

    Time frame: Βaseline and two days after the final training session at four weeks

  11. Change in VO2peak

    Physiological markers were assessed pre- and post-exercise, including VO2peak.

    Time frame: Βaseline and two days after the final training session at four weeks

Secondary outcomes

  1. Change in body mass

    Body composition changes, including body mass (kg).

    Time frame: Baseline and two days after the final training session at four weeks

  2. Change in body-fat percentage

    Body composition changes, body-fat percentage (%).

    Time frame: Baseline and two days after the final training session at four weeks

07

Study locations

1 site
  • Athens Olympic Aquatic Centre (OAKA)
    Athens, Attica 15123, Greece
08

References and documents

Publications

  • Mavropoulos A, Bersimis F, Ploumidou V, Koutsouki D, Kourtessis T, Soultanakis H. Effects of High-Intensity vs. High-Volume Training on Repeated Sprint Ability in Competitive Paraswimmers. Research Square. 2025. https://doi.org/10.21203/rs.3.rs-7419128/v1

Individual participant data

Plan to share: No — Individual participant data are not planned for public release because the small sample size and detailed sport-class information may create a risk of participant re-identification. De-identified aggregate data and additional study information may be available from the corresponding author upon reasonable request and subject to ethical and institutional approval.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Sep 2022 to primary completion in Nov 2022, 2 months.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 24, 2026
First posted
Oct 7, 2026
StartActual
Sep 1, 2022
Primary completionActual
Nov 30, 2022
CompletionActual
Dec 15, 2022
Last update
Oct 7, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 7, 2026
Show all 1 update
  1. Oct 7, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07862036
Responsible party
Aris Mavropoulos (Principal Investigator, PhD Candidate, National and Kapodistrian University of Athens) — Principal investigator
First posted
Oct 7, 2026
Start date
Sep 1, 2022
Primary completion
Nov 30, 2022
Completion
Dec 15, 2022
Last update
Oct 7, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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