Predictors of Affective Responses to Sprint Interval Exercise

NCT05260905 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2026-04-29

No results posted yet for this study

Summary

Regular exercise is needed to ensure good general health and wellbeing. How exercise makes you feel (pleasant / unpleasant) is thought to be important for whether people will stick with a given exercise routine. Sprint interval training (SIT) has been shown be a time-efficient exercise strategy for improving health, but some researchers suggest that SIT may be experienced as unpleasant and therefore unsuitable as an exercise routine for improving general health and wellbeing. However, SIT protocols are diverse, and it has previously been shown that very short SIT protocols such as 'reduced-exertion high-intensity interval training' (REHIT) are not perceived as unpleasant, at least on average. Interestingly, how REHIT is perceived appears to be highly variable between individuals. This individual variability may have important implications for whether people stick with REHIT and/or SIT in real-world settings, and therefore it is important to characterise it and better understand why some people find this exercise unpleasant while others do not. This study aims to characterise the within-participant and between-participant variability in how people perceive REHIT. Furthermore, potential relationships between psychological characteristics and how people perceive REHIT will be explored.

Conditions

  • General Health

Interventions

BEHAVIORAL

REHIT

REHIt involves 10 minutes of unloaded cycling on a stationary bike, interspersed with two 20-s 'all-out' cycle sprints against a resistance equivalent to 7.5% of body mass.

Sponsors & Collaborators

  • Swansea University

    collaborator OTHER
  • University of Worcester

    collaborator OTHER
  • University of Edinburgh

    collaborator OTHER
  • California State University, San Marcos

    collaborator OTHER
  • University of Stirling

    lead OTHER

Principal Investigators

  • Niels Vollaard, PhD · University of Stirling

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-01
Primary Completion
2025-05-30
Completion
2025-08-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05260905 on ClinicalTrials.gov