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CompletedNCT07926451Updated Nov 9, 2026

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

An interventional study of Sprint Interval Training with 60-Second Recovery (SIT10:1) and Sprint Interval Training with 240-Second Recovery (SIT10:4) in Exercise-Induced Physiological Adaptations, sponsored by Gdansk University of Physical Education and Sport. Completed at 1 site in Poland. Open to male participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-09.

Sponsored by Gdansk University of Physical Education and Sport · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 13 years 8 months after the study started (first participant enrolled Feb 2013, registered Nov 2026).
Updated Nov 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Non-randomized
Ages
18 Years to 35 Years
Sex
Male
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Exercise-Induced Physiological Adaptations

Keywords

  • High-Intensity Interval Training
  • Sprint Interval Training
  • Aerobic Fitness
  • Skeletal Muscle Adaptations
  • Cognitive Function
03

In context

Lead sponsor

Gdansk University of Physical Education and Sport is the lead sponsor of 37 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Male
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

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 .

Exclusion criteria

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 to maximal exercise testing or sprint interval training.

Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    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.

    Behavioral: Sprint Interval Training with 60-Second Recovery (SIT10:1)

  • Experimental
    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.

    Behavioral: Sprint Interval Training with 240-Second Recovery (SIT10:4)

  • Experimental
    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.

    Behavioral: High-Intensity Interval Training (HIIT90:180)

  • Experimental
    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.

    Behavioral: Wingate-Based Sprint Interval Training (Wingate-SIT)

Interventions

  • BehavioralSprint Interval Training with 60-Second Recovery (SIT10:1)

    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.

  • BehavioralSprint Interval Training with 240-Second Recovery (SIT10:4)

    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.

  • BehavioralHigh-Intensity Interval Training (HIIT90:180)

    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.

  • BehavioralWingate-Based Sprint Interval Training (Wingate-SIT)

    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.

06

What researchers measure

Primary outcomes

  1. Change in Maximal Oxygen Uptake (VO2max)

    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.

    Time frame: Baseline and after the 2-week training intervention

Secondary outcomes

  1. Change in Cognitive Performance

    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.

    Time frame: Baseline and after the 2-week training intervention

  2. Change in Skeletal Muscle Oxidative Enzyme Activity

    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.

    Time frame: Baseline and after the 2-week training intervention

07

Study locations

1 site
  • Gdansk University of Physical Education and Sport
    Gdansk, Pomeranian 80-336, Poland
08

References and documents

Individual participant data

Plan to share: No — 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.

No publications or documents are linked to this record.

09

Timeline

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

Ran from Feb 2013 to primary completion in Apr 2018, 62 months.

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

Registered
Nov 4, 2026
First posted
Nov 9, 2026
StartActual
Feb 10, 2013
Primary completionActual
Apr 17, 2018
CompletionActual
Dec 30, 2018
Last update
Nov 9, 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
Nov 9, 2026
Show all 1 update
  1. Nov 9, 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
NCT07926451
Lead sponsor
Gdansk University of Physical Education and Sport
Responsible party
Sponsor
First posted
Nov 9, 2026
Start date
Feb 10, 2013
Primary completion
Apr 17, 2018
Completion
Dec 30, 2018
Last update
Nov 9, 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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This study is completed, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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