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

6 novembre 2026 mis à jour par: APOSTOLOS PAPANDREOU, National and Kapodistrian University of Athens

Physiological and Molecular Responses to Different Intensities of High-Intensity Interval Training and Continuous Training in National-Level Kayak Athletes

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 This interventional study investigated physiological, systemic biomarker, and performance responses to different training modalities in national-level flatwater kayak athletes. Thirty-two athletes (24 males and 8 females) were randomly allocated within sex strata to four parallel groups: high-intensity interval training (HIIT), sprint interval training (SIT), combined training (COMB), and control (CON), with eight participants per group (six males and two females).

The study included an initial six-week detraining period, baseline (PRE) assessments, a six-week training intervention, and post-intervention (POST) assessments. POST venous blood samples were collected 48-72 hours after the final training session, following a recovery period. Physiological and performance assessments were conducted during the POST testing period.

Following the intervention, participants underwent a further six-week detraining period. Kayak performance over 500 m was assessed at PRE and POST and reassessed 15 and 30 days after the beginning of the post-intervention detraining period.

The study aimed to compare the effects of different training modalities on physiological responses, circulating systemic biomarkers, and 500-m kayak performance, as well as performance changes during detraining.

Aperçu de l'étude

Description détaillée

This study employed a sex-stratified randomized, four-parallel-group interventional design to investigate physiological, systemic biomarker, and performance responses to different training modalities in national-level flatwater kayak athletes.

Thirty-two athletes (24 males and 8 females), each with at least four years of kayaking experience, participated in the study. Participants were initially stratified according to sex and subsequently randomly allocated by drawing lots to four parallel groups: high-intensity interval training (HIIT), sprint interval training (SIT), combined training (COMB), and control (CON). Each group comprised eight athletes (six males and two females). Baseline 500-m performance, maximal oxygen uptake (VO2max), body mass, and training experience were not used as matching or allocation criteria. Participants were not reassigned after randomization to achieve baseline equivalence.

Before baseline (PRE) assessments, participants completed a six-week detraining period. PRE assessments were conducted between December 20 and 23, 2024. The six-week training intervention commenced on December 26, 2024, with three scheduled sessions per week.

The HIIT group performed six 30-second intervals at a power output corresponding to 110% of the power output associated with VO2max, separated by 60-second recovery periods. The SIT group performed six 15-second intervals at approximately 140% of the power output associated with VO2max, separated by 150-second recovery periods. The COMB group completed one HIIT session, one SIT session, and one 45-minute continuous training session at 80% of the power output associated with VO2max per week. The CON group performed three 60-minute walking sessions per week.

Physiological assessments were performed before (PRE) and after (POST) the intervention and included maximal oxygen uptake (VO2max), power output associated with maximal oxygen uptake (POVO2max), power output at the second ventilatory threshold (POVT2), blood lactate concentration, and maximal heart rate (HRmax). Additional physiological outcomes, including power output corresponding to 75% of VO2max, were assessed as specified in the original study protocol.

Venous blood samples were collected at PRE and POST to assess circulating biomarkers 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).

Importantly, POST venous blood sampling was performed 48-72 hours after the final training session of the six-week intervention, following a recovery period without additional training sessions. The POST physiological assessments were conducted subsequently, during the post-intervention testing period. Therefore, the POST blood samples were not collected immediately after the final exercise session.

A maximal-effort 500-m kayak ergometer performance test was conducted at PRE and POST. Following completion of the intervention and POST assessments, participants underwent a further six-week detraining period. Additional 500-m performance assessments were conducted 15 and 30 days after the beginning of this subsequent detraining period to evaluate the retention of training-induced performance adaptations.

The original intervention involved all 32 athletes. A subsequent secondary analysis restricted to the 24 male athletes (six per group) examined circulating systemic biomarker responses and their associations with physiological adaptations to the different training modalities.

Type d'étude

Interventionnel

Inscription (Réel)

32

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Attica
      • Athens, Attica, Grèce, 17237
        • National and Kapodistrian University of Athens

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

16 ans à 28 ans (Enfant, Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

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:

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.

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.

Autres noms:
  • HIIT
Expérimental: 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.

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.

Autres noms:
  • S'ASSEOIR
Expérimental: 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.

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.

Autres noms:
  • PEIGNE
Comparateur actif: 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.

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

Autres noms:
  • CONTRE

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in maximal oxygen uptake (VO₂max)
Délai: Baseline (PRE) and during the post-intervention (POST) assessment period following the 6-week training intervention.

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.

Baseline (PRE) and during the post-intervention (POST) assessment period following the 6-week training intervention.
500-m kayak performance
Délai: Baseline (PRE), post-intervention (POST), and 15 and 30 days after the start of the subsequent 6-week detraining period.

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

Baseline (PRE), post-intervention (POST), and 15 and 30 days after the start of the subsequent 6-week detraining period.
Change in power output at VO₂max (POVO₂max)
Délai: Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.

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.

Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.
Change in power output at the second ventilatory threshold (POVT₂)
Délai: Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.

Power output at the second ventilatory threshold (POVT₂) was determined during an incremental kayak ergometer test conducted before (PRE) and after (POST) the 6-week training intervention. VT₂ was identified from ventilatory and gas-exchange responses, and the corresponding power output was expressed in watts (W). Changes in POVT₂ were used to evaluate submaximal aerobic adaptations to the different training interventions.

Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.
Change in power output at 75% of VO₂max (PO75%VO₂max)
Délai: Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.

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).

Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.
Change in blood lactate concentration
Délai: Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.

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.

Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.
Change in maximal heart rate (HRmax)
Délai: Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.

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).

Baseline (PRE) and during the POST testing period, following venous blood sampling performed 48-72 hours after the final training session.
Change in circulating interleukin-6 (IL-6)
Délai: Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.

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.

Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.
Change in circulating vascular endothelial growth factor A (VEGF-A)
Délai: Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.

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.

Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.
Change in circulating hypoxia-inducible factor-1 alpha (HIF-1α)
Délai: Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.

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.

Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.
Change in total antioxidant capacity (TAC)
Délai: Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.

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.

Baseline (PRE) and 48-72 hours after the final training session (POST), following the 6-week intervention.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

8 novembre 2024

Achèvement primaire (Réel)

23 avril 2025

Achèvement de l'étude (Réel)

23 avril 2025

Dates d'inscription aux études

Première soumission

30 septembre 2026

Première soumission répondant aux critères de contrôle qualité

6 octobre 2026

Première publication (Réel)

7 octobre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 novembre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Individual participant data (IPD) will not be shared because participant consent did not include provisions for public or unrestricted sharing of individual-level data.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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