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TerminatedNCT05249205Updated May 5, 2026

The Effect of Training Frequency on Improvements in VO2max With REHIT

An interventional study of REHIT1 and REHIT2 in General Health, sponsored by University of Stirling. Terminated at 3 sites in United Kingdom. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-05.

Sponsored by University of Stirling · Not applicable, Interventional, and Prevention

Why this study was terminated
Insufficient recruitment
Phase
Not applicable
Study type
Interventional
Enrollment
15
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

Many people do not manage to do the recommended amount of physical activity for improving general health and wellbeing, and a common reason for this is lack of time. Sprint interval training (SIT) has been suggested to be a time-efficient alternative to current exercise recommendations, but most SIT protocols are not actually as time-efficient as claimed. However, it has previously been shown that the training time commitment of common SIT protocols can be substantially reduced while remaining effective at improving key health markers such as aerobic fitness, insulin function and blood pressure. For example, the reduced-exertion high-intensity interval training (REHIT) protocol consists of two 20-second 'all-out' cycle sprints within a 10-minute low-intensity exercise session. There is some evidence that REHIT is just as effective at improving aerobic fitness with 2 exercise sessions per week compared to 3 or 4 sessions. However, it remains unknown if improvements in aerobic fitness are reduced if just a single REHIT session is performed each week. Therefore, the aim of the present study is to compare improvements in aerobic fitness levels between a control group (no training intervention), a group performing a single REHIT session per week, and a group performing 2 REHIT sessions per week.

Read the detailed description

Up to 45 apparently healthy participants will be recruited at multiple sites. Eligible participants will complete a fitness test to measure pre-training maximal aerobic capacity (V̇O2max). Participants will start cycling on a stationary bike at a low intensity (30 W). The intensity will increase by 1 W every 3 seconds until volitional exhaustion or an inability to maintain a pedalling frequency of >60 rpm. Expired O2 and CO2 will be continuously measured breath-by-breath using an online gas analyser. V̇O2max will be determined as the highest value for a 15-breath rolling average of V̇O2. V̇O2max will be accepted if at least 2 of the following criteria are met: volitional exhaustion / inability to maintain a pedal frequency of 60 rpm, RER>1.10, a plateau in V̇O2, and/or heart rate within 10 bpm of the age predicted maximum (220-age).

Participants will then be randomised into one of 3 groups, performing either 1 or 2 REHIT training sessions per week, or no training intervention (control group). Randomisation will be performed using the sealed envelope method. Participants in the control group will be asked to maintain their regular lifestyle for 6 weeks. Participants in the training groups will perform 6 weeks of REHIT. Each REHIT session involves 10 min of unloaded pedalling interspersed with 2 all-out cycle sprints against a resistance equivalent to 7.5% of the participant's body weight. Sprint duration will be 10 s in week 1, 15 s in week 2, and 20 s in the remaining 4 weeks. The first sprint will finish at 2 min and the second sprint will finish at 6 min. Participants will be instructed to start pedalling as fast as they can \~2-3 s before applying the sprint resistance, and to keep pedalling as fast as they can during the sprint. Verbal encouragement will be provided. Heart rate and power output will be measured throughout each 10-minute exercise session. The post-training V̇O2max test will be scheduled 3 days following the last training session.

02

Conditions studied

  • General Health

Keywords

  • Reduced-exertion high-intensity interval training
  • REHIT
  • Training frequency
  • Fitness
03

In context

Lead sponsor

University of Stirling is the lead sponsor of 23 studies on the registry; 2 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 40 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

  • Apparently healthy
  • Sedentary or recreationally active

Exclusion criteria

Exclusion Criteria:

  • Classified as highly physically active on the International Physical Activity Questionnaire (IPAQ)
  • Answering 'Yes' to any of the questions of a standard Physical Activity Readiness Questionnaire (PAR-Q)
  • Resting heart rate >100 bpm
  • Resting blood pressure > 140/90 mm Hg
  • > 35 kg/m2
  • Testing positive for Covid-19
  • Pregnant women
Terms in these criteria, in plain language(1)

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.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

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

Study arms

  • No intervention
    Control

    Participants in the control group will be asked to maintain their regular lifestyle for the duration of the study. They will not receive an intervention.

  • Experimental
    REHIT1

    Participants in the REHIT1 group will perform a single REHIT session per week for 6 weeks.

    Behavioral: REHIT1

  • Experimental
    REHIT2

    Participants in the REHIT2 group will perform 2 REHIT sessions per week for 6 weeks.

    Behavioral: REHIT2

Interventions

  • BehavioralREHIT1

    This intervention involves a single REHIT exercise session per week. REHIT involves 10 minutes of unloaded cycling on a stationary bike interspersed with two 20-second 'all-out' cycle sprints against a resistance equivalent to 7.5% of body mass.

    Also known as: Reduced-exertion high-intensity interval training / single session per week

  • BehavioralREHIT2

    This intervention is the same as that for the REHIT1 intervention, but with 2 sessions per week instead of 1.

    Also known as: Reduced-exertion high-intensity interval training / 2 sessions per week

06

What researchers measure

Primary outcomes

  1. Change in maximal aerobic capacity (VO2max)

    VO2max is the greatest volume of oxygen an individual can consume per minute. It is a key health marker.

    Time frame: Pre-intervention and 3 days following completion of the intervention.

07

Study locations

3 sites
  • University of Stirling
    Stirling, Stirlingshire FK9 4LA, United Kingdom
  • University of Worcester
    Worcester, Worcestershire, United Kingdom
  • Swansea University
    Swansea, SA1 8EN, United Kingdom
08

References and documents

Individual participant data

Plan to share: Yes — Anonymised IPD can be provided to other researchers on request, if the data are of use to answer a valid research question.

Supporting information: Study protocol, Statistical analysis plan

Time frame: After completion of data collection.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05249205
Lead sponsor
University of Stirling
Collaborators
Swansea University, University of Worcester
Responsible party
Niels Vollaard (Principal investigator, University of Stirling) — Principal investigator
First posted
Feb 21, 2022
Start date
Feb 21, 2022
Primary completion
May 30, 2025
Completion
Aug 30, 2025
Last update
May 5, 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 terminated, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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