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CompletedNCT07864012Updated Oct 7, 2026

Physiological and Molecular Adaptations to Different Training Modalities in National-level Kayak Athletes

An interventional study of High-Intensity Interval Training and Sprint Interval Training in Exercise Training Adaptation, sponsored by National and Kapodistrian University of Athens. Completed at 1 site in Greece. Open to participants aged 16 Years to 28 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-07.

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

From the registry’s dates

  • Registered 1 year 10 months after the study started (first participant enrolled Nov 2024, registered Sep 2026).
Updated Oct 7, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
16 Years to 28 Years
Sex
All
01

Study summary

This interventional study evaluated physiological, molecular, and performance adaptations to different high-intensity training modalities in national-level kayak athletes. Thirty-two athletes were allocated to four parallel groups: high-intensity interval training (HIIT), sprint interval training (SIT), combined training (COMB), or a control condition (CON). The study protocol included a six-week detraining period before baseline (PRE) assessments, followed by a six-week training intervention and a subsequent six-week detraining period. Physiological assessments and blood sampling were performed at PRE and immediately after the training intervention (POST) to evaluate training-related changes. Sprint kayak performance over 500 m was assessed at PRE and POST, with additional assessments conducted 15 and 30 days after completion of the subsequent six-week detraining period. The study aimed to examine the effects of different training modalities on physiological responses, circulating molecular markers, and 500-m kayak performance, as well as changes in performance following detraining.

Read the detailed description

This study used a matched randomized, four-parallel-group interventional design to investigate physiological, molecular, and performance adaptations to different training modalities in national-level kayak athletes. Thirty-two athletes (24 males and 8 females), each with at least four years of kayaking experience, participated in the study.

Before baseline (PRE) assessments, participants completed a six-week detraining period. Participants were subsequently matched according to sex and baseline 500-m performance and allocated by randomization to one of four parallel groups: high-intensity interval training (HIIT), sprint interval training (SIT), combined training (COMB), or control (CON). Each group consisted of eight athletes (six males and two females).

The training intervention lasted six weeks, with three scheduled sessions per week. The HIIT group performed 6 x 30-s intervals at 110% of VO2max with 60-s recovery periods. The SIT group performed 6 x 15-s intervals at approximately 140% of VO2max with 150-s recovery periods. The COMB group performed one HIIT session, one SIT session, and one 45-min continuous training session at 80% of VO2max per week. The CON group performed three 1-h walking sessions per week.

Physiological assessments were performed before (PRE) and immediately after (POST) the training intervention and included maximal oxygen uptake (VO2max), power output associated with maximal oxygen uptake (POVO2max), power output at the second ventilatory threshold (POVT2), power output corresponding to 75% of VO2max, blood lactate concentration, and maximal heart rate.

Blood samples were collected at PRE and POST to assess circulating markers related to inflammatory, angiogenic, hypoxia-related, and antioxidant responses, including interleukin-6 (IL-6), vascular endothelial growth factor A (VEGF-A), hypoxia-inducible factor-1 alpha (HIF-1 alpha), and total antioxidant capacity (TAC).

A 500-m kayak performance test was conducted at PRE and POST. Following completion of the POST assessments, participants completed a subsequent six-week detraining period. Additional 500-m performance assessments were conducted 15 and 30 days after completion of the six-week detraining period to assess changes in 500-m performance following detraining.

02

Conditions studied

  • Exercise Training Adaptation

Keywords

  • sprint kayaking
  • High-Intensity Interval Training
  • Sprint Interval Training
  • Exercise Physiology
  • Physiological Adaptations
  • Molecular Adaptations
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
16 Years to 28 Years
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

  • National-level flatwater kayak athlete.
  • At least 4 years of systematic kayak training experience.
  • Active participation in kayak training and competition.
  • Able to complete the prescribed training interventions and physiological and performance testing procedures.

Exclusion criteria

Exclusion Criteria:

  • Injury or illness that prevented participation in the training intervention or testing procedures.
  • Inability to complete the prescribed intervention or required study assessments.
05

Study design

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

Study arms

  • Experimental
    High-Intensity Interval Training (HIIT)

    Participants performed high-intensity interval training three times per week for six weeks. Each session included 6 × 30-s intervals at 110% of VO₂max with 60-s passive recovery periods.

    Behavioral: High-Intensity Interval Training

  • Experimental
    Sprint Interval Training (SIT)

    Participants performed sprint interval training three times per week for six weeks. Each session included 6 × 15-s intervals at approximately 140% of VO₂max with 150-s passive recovery periods.

    Behavioral: Sprint Interval Training

  • Experimental
    Combined Training (COMB)

    Participants performed combined training for six weeks, consisting of one HIIT session, one SIT session, and one 45-min continuous training session at 80% of VO₂max per week.

    Behavioral: Combined High-Intensity and Continuous Training

  • Active comparator
    Control (CON)

    Participants performed three 1-h walking sessions per week for six weeks and did not participate in the experimental high-intensity training protocols.

    Behavioral: Control

Interventions

  • BehavioralHigh-Intensity Interval Training

    Participants performed high-intensity interval training three times per week for six weeks. Each training session consisted of 6 × 30-second intervals at 110% of VO₂max, with 60-second recovery periods between intervals.

    Also known as: HIIT

  • BehavioralSprint Interval Training

    Participants performed sprint interval training three times per week for six weeks. Each training session consisted of 6 × 15-second intervals at approximately 140% of VO₂max, with 150-second recovery periods between intervals.

    Also known as: SIT

  • BehavioralCombined High-Intensity and Continuous Training

    Participants performed combined training for six weeks, with three training sessions per week. The weekly program consisted of one high-intensity interval training session (6 × 30-second intervals at 110% of VO₂max with 60-second recovery periods), one sprint interval training session (6 × 15-second intervals at approximately 140% of VO₂max with 150-second recovery periods), and one 45-minute continuous training session at 80% of VO₂max.

    Also known as: COMB

  • BehavioralControl

    Participants performed three 1-hour walking sessions per week for six weeks and did not participate in the experimental high-intensity training protocols.

    Also known as: CON

06

What researchers measure

Primary outcomes

  1. Change in maximal oxygen uptake (VO₂max)

    Maximal oxygen uptake (VO₂max) was assessed using an incremental kayak ergometer test before (PRE) and after (POST) the 6-week intervention. VO₂max was used to evaluate changes in aerobic physiological capacity following the different training interventions.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  2. 500-m kayak performance

    Time required to complete a 500-m maximal-effort kayak ergometer performance test, recorded in seconds. Lower values indicate faster performance.

    Time frame: Baseline (PRE), immediately after the 6-week intervention (POST), and 15 and 30 days after completion of the 6-week detraining period

  3. Change in power output at VO₂max (POVO₂max)

    Power output at VO₂max (POVO₂max) was assessed during the incremental kayak ergometer test before (PRE) and after (POST) the 6-week intervention. The outcome was expressed in watts (W) and used to evaluate changes in maximal aerobic power.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  4. Change in power output at the second ventilatory threshold (POVT₂)

    Power output at the second ventilatory threshold (POVT₂) was determined during the incremental kayak ergometer test before (PRE) and after (POST) the 6-week intervention. The outcome was expressed in watts (W) and used to evaluate changes in submaximal aerobic performance.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  5. Change in power output at 75% of VO₂max (PO75%VO₂max)

    Power output corresponding to 75% of VO₂max was determined from the oxygen uptake-power relationship obtained during the incremental kayak ergometer test before (PRE) and after (POST) the 6-week intervention. The outcome was expressed in watts (W).

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  6. Change in blood lactate concentration

    Blood lactate concentration was measured 3 minutes after completion of the incremental kayak ergometer test before (PRE) and after (POST) the 6-week intervention. The outcome was expressed in mmol/L.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  7. Change in maximal heart rate (HRmax)

    Maximal heart rate (HRmax) was recorded during the incremental kayak ergometer test before (PRE) and after (POST) the 6-week intervention. The outcome was expressed in beats per minute (bpm).

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  8. Change in circulating interleukin-6 (IL-6)

    Serum interleukin-6 (IL-6) concentration was assessed from venous blood samples collected before (PRE) and after (POST) the 6-week intervention to evaluate changes in the circulating inflammatory response.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  9. Change in circulating vascular endothelial growth factor A (VEGF-A)

    Serum vascular endothelial growth factor A (VEGF-A) concentration was assessed from venous blood samples collected before (PRE) and after (POST) the 6-week intervention to evaluate changes in the circulating angiogenic response.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  10. Change in circulating hypoxia-inducible factor-1 alpha (HIF-1α)

    Serum hypoxia-inducible factor-1 alpha (HIF-1α) concentration was assessed from venous blood samples collected before (PRE) and after (POST) the 6-week intervention to evaluate changes in the circulating hypoxia-related response.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

  11. Change in total antioxidant capacity (TAC)

    Serum total antioxidant capacity (TAC) was assessed from venous blood samples collected before (PRE) and after (POST) the 6-week intervention to evaluate changes in systemic antioxidant capacity.

    Time frame: Baseline (PRE) and immediately after the 6-week intervention (POST)

07

Study locations

1 site
  • National and Kapodistrian University of Athens
    Athens, Attica 17237, Greece
08

References and documents

Publications

  • Papandreou A, Paradisis G, Philippou A, Zacharogiannis E. Contribution of Aerobic Physiological Variables to 500 m Sprint Kayak Performance in National-Level Athletes: A Hierarchical Regression Analysis. Sports (Basel). 2026 Aug 20;14(8):363. doi: 10.3390/sports14080363. PubMed 42646900 ↗

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared because participant consent did not include provisions for public or unrestricted sharing of individual-level data.

09

Timeline

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

Ran from Nov 2024 to primary completion in Apr 2025, 5 months.

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

Registered
Sep 30, 2026
First posted
Oct 7, 2026
StartActual
Nov 8, 2024
Primary completionActual
Apr 23, 2025
CompletionActual
Apr 23, 2025
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
NCT07864012
Responsible party
APOSTOLOS PAPANDREOU (Doctoral Candidate, National and Kapodistrian University of Athens) — Principal investigator
First posted
Oct 7, 2026
Start date
Nov 8, 2024
Primary completion
Apr 23, 2025
Completion
Apr 23, 2025
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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