Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Effects of Different High-Intensity Interval Training Protocols on Physiological and Skeletal Muscle Adaptations in Healthy Young Men

This study investigated the effects of different high-intensity interval training protocols on physical fitness and physiological adaptations in healthy young men.

Participants underwent a two-week exercise training program consisting of six sessions performed three times per week. Four training protocols were investigated, differing in exercise intensity, duration of exercise bouts, and recovery periods.

The primary outcome was the change in maximal oxygen uptake (VO2max), an indicator of aerobic fitness. Additional assessments included cognitive performance, measured using tests of attention, processing speed, and inhibitory control, as well as selected physiological and skeletal muscle adaptations.

The study aimed to improve understanding of how different high-intensity interval training protocols influence aerobic fitness and other physiological responses over a short training period.

Studieöversikt

Detaljerad beskrivning

High-intensity interval training (HIIT) and sprint interval training (SIT) are exercise strategies characterized by repeated bouts of vigorous or maximal exercise interspersed with recovery periods. These training approaches may induce physiological adaptations within relatively short intervention periods. However, the effects of different combinations of exercise duration, intensity, and recovery time on aerobic fitness, cognitive performance, and skeletal muscle adaptations require further investigation.

This interventional study examined physiological responses to four cycling-based high-intensity training protocols in healthy young men. Participants completed six training sessions over two weeks, with three sessions performed each week.

The investigated protocols included:

SIT10:1: Repeated 10-second maximal cycling sprints separated by 60-second recovery periods.

SIT10:4: Repeated 10-second maximal cycling sprints separated by 240-second recovery periods.

HIIT90:180: Six 90-second cycling intervals performed at 80% of maximal aerobic power, separated by 180-second passive recovery periods.

Wingate-SIT: Repeated 30-second all-out cycling sprints using a Wingate-based protocol.

The primary outcome was the change in maximal oxygen uptake (VO2max), assessed using incremental exercise testing before and after the intervention. Additional assessments included cognitive performance using the Stroop Color-Word Test, Trail Making Test, and Digit Span Test, as well as selected measures of exercise performance and skeletal muscle metabolic adaptations.

Skeletal muscle biopsies were collected from subsets of participants before and after training to investigate exercise-induced adaptations in muscle tissue. Stored biopsy samples were subsequently used for exploratory proteomic analyses.

The study was designed to characterize short-term physiological and skeletal muscle responses to different high-intensity interval exercise protocols.

Studietyp

Interventionell

Inskrivning (Faktisk)

50

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Pomeranian
      • Gdansk, Pomeranian, Polen, 80-336
        • Gdansk University of Physical Education and Sport

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år till 35 år (Vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Manlig

Beskrivning

Inclusion Criteria:

Healthy adult males. Physically active individuals. Ability to perform high-intensity cycling exercise. Willingness to participate in the two-week training intervention and complete the required assessments.

Provision of written informed consent.

Exclusion Criteria:

Known cardiovascular, respiratory, metabolic, or neurological disorders that could affect exercise performance or participant safety.

Musculoskeletal injuries or conditions preventing participation in high-intensity cycling exercise.

Medical contraindications to maximal exercise testing or sprint interval training.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Grundläggande vetenskap
  • Tilldelning: Icke-randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: SIT10:1 - Short-Recovery Sprint Interval Training

Participants completed a two-week cycling sprint interval training program comprising six sessions (three sessions per week). The protocol involved repeated 10-second maximal cycling sprints separated by 60-second recovery intervals.

A two-week cycling sprint interval training intervention consisting of six sessions performed three times per week. Participants performed repeated 10-second maximal cycling sprints interspersed with 60-second recovery intervals.

Experimentell: SIT10:4 - Long-Recovery Sprint Interval Training

Participants completed a two-week cycling sprint interval training program comprising six sessions (three sessions per week). The protocol involved repeated 10-second maximal cycling sprints separated by 240-second recovery intervals.

A two-week cycling sprint interval training intervention consisting of six sessions performed three times per week. Participants performed repeated 10-second maximal cycling sprints interspersed with 240-second recovery intervals.

Experimentell: HIIT90:180 - High-Intensity Interval Training

Participants completed a two-week high-intensity interval cycling program consisting of six supervised training sessions (three sessions per week). Each session included six 90-second cycling bouts performed at 80% of maximal aerobic power, separated by 180-second passive recovery intervals. Exercise cadence was maintained at approximately 60 revolutions per minute.

A two-week cycling high-intensity interval training intervention comprising six supervised sessions performed three times per week. Each session consisted of six 90-second exercise bouts at 80% of maximal aerobic power, separated by 180-second passive recovery intervals. Cycling cadence was approximately 60 revolutions per minute.

Experimentell: Wingate-SIT - Wingate-Based Sprint Interval Training

Participants completed a two-week sprint interval training program comprising six cycling sessions (three sessions per week). The intervention consisted of repeated 30-second all-out cycling sprints performed using a Wingate-based protocol, with recovery periods between successive efforts.

A two-week cycling sprint interval training intervention comprising six sessions performed three times per week. Participants performed repeated 30-second all-out cycling sprints using a Wingate-based protocol, with recovery intervals between successive sprints.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Maximal Oxygen Uptake (VO2max)
Tidsram: Baseline and after the 2-week training intervention

Change in maximal oxygen uptake (VO2max), expressed in mL/kg/min, assessed using an incremental exercise test before and after the two-week training intervention.

Baseline and after the 2-week training intervention

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Cognitive Performance
Tidsram: Baseline and after the 2-week training intervention

Changes in cognitive performance assessed using the Stroop Color-Word Test (inhibitory control), Trail Making Test (processing speed and executive function), and Digit Span Test (working memory), before and after the two-week training intervention.

Baseline and after the 2-week training intervention
Change in Skeletal Muscle Oxidative Enzyme Activity
Tidsram: Baseline and after the 2-week training intervention

Changes in skeletal muscle oxidative enzyme activity assessed in biopsy samples collected before and after the two-week training intervention. Muscle biopsies were performed in a subset of participants who provided additional informed consent for the procedure.

Baseline and after the 2-week training intervention

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

10 februari 2013

Primärt slutförande (Faktisk)

17 april 2018

Avslutad studie (Faktisk)

30 december 2018

Studieregistreringsdatum

Först inskickad

4 november 2026

Först inskickad som uppfyllde QC-kriterierna

4 november 2026

Första postat (Faktisk)

9 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

9 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

4 november 2026

Senast verifierad

1 november 2026

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

IPD-planbeskrivning

Individual participant data will not be made publicly available due to participant confidentiality considerations and the absence of a data-sharing plan in the original study protocol.

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera