NCT07582718

Brief Summary

This study aims to evaluate the effects of a supervised whole-body high-intensity interval training (WB-HIIT) program on physical fitness and health outcomes in adults with overweight and obesity. WB-HIIT is a practical and time-efficient training modality based on body-weight exercises performed at high intensity with short recovery intervals. It may offer an accessible approach for improving health in individuals with excess body weight. Participants aged 18 to 55 years with a body mass index (BMI) between 25 and 35 kg/m² will take part in a supervised 10-week WB-HIIT program, performed in small groups and led by trained exercise professionals. Before and after the intervention, participants will undergo assessments including DXA-based body composition analysis, fasting blood sampling, muscular strength testing, a Chester step test, a maximal graded treadmill exercise test with gas-exchange analysis to determine VO₂peak, and functional evaluations (chair-stand, arm-curl, and 6-minute walk test). Physical activity and dietary intake will also be recorded. The primary objective of the study is to assess whether WB-HIIT improves cardiorespiratory fitness (VO₂peak) in adults with overweight. Secondary objectives include evaluating changes in muscular strength, body composition, metabolic markers, and functional capacity. The results may help determine whether an equipment-free WB-HIIT program can serve as an effective and accessible training approach for improving health and physical fitness in adults with overweight and obesity.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
0mo left

Started Nov 2022

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress99%
Nov 2022Jun 2026

Study Start

First participant enrolled

November 9, 2022

Completed
3.3 years until next milestone

First Submitted

Initial submission to the registry

February 19, 2026

Completed
3 months until next milestone

First Posted

Study publicly available on registry

May 13, 2026

Completed
19 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Last Updated

May 13, 2026

Status Verified

May 1, 2026

Enrollment Period

3.6 years

First QC Date

February 19, 2026

Last Update Submit

May 11, 2026

Conditions

Keywords

OverweightCardiorespiratory FitnessBody CompositionMuscular StrengthWhole-Body HIITBody-Weight ExerciseMetabolic health

Outcome Measures

Primary Outcomes (2)

  • Peak oxygen consumption (VO₂peak)

    Peak oxygen consumption (VO₂peak) will be measured during a maximal graded treadmill exercise test with gas analysis to assess changes in cardiorespiratory fitness following the 10-week WB-HIIT program. VO₂peak will be expressed in mL·kg-¹·min-¹.

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

  • Muscular strength

    Maximal dynamic strength will be assessed using 3-repetition maximum (3-RM) tests on the leg press and bench press.

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

Secondary Outcomes (13)

  • Estimated VO₂max from the Chester Step Test

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

  • Body composition

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

  • Muscular endurance (fatigue tests at 60% 1-RM)

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

  • Functional performance (chair-stand test)

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

  • Upper-body functional performance (arm-curl test)

    The outcome will be assessed once at baseline and within 72 hours after the last session of the whole-body high-intensity interval training intervention.

  • +8 more secondary outcomes

Study Arms (2)

WB-HIIT Intervention

EXPERIMENTAL

A supervised whole-body high-intensity interval training (WB-HIIT) program performed in small groups. Participants complete 2 to 3 sessions per week for 10 weeks. Each session includes a warm-up followed by 8 to 12 whole-body exercises performed at high intensity for 20-60 seconds with recovery periods of 20-60 seconds. Progression is applied by adjusting exercise complexity, number of sets, and work-to-rest ratio. Heart rate and perceived exertion (Borg CR-10 scale) are monitored.

Behavioral: Whole-Body High-Intensity Interval Training (WB-HIIT)

Control Group

NO INTERVENTION

Participants in the control group do not receive structured exercise training. They maintain their usual lifestyle and complete the same pre- and post-intervention assessments as the intervention group.

Interventions

A structured WB-HIIT program using body-weight exercises such as squats, lunges, mountain climbers, and similar multi-joint movements. Sessions last 35-50 minutes and include 3 to 4 sets of interval blocks performed at high intensity. The training is supervised by qualified exercise professionals.

WB-HIIT Intervention

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Adults aged 18 to 55 years.
  • Body mass index (BMI) between 25 and 35 kg/m².
  • Able to provide written informed consent.
  • Able to safely participate in high-intensity interval training.
  • For participants with BMI \> 30 kg/m²: medical clearance from their general practitioner.

You may not qualify if:

  • BMI \< 25 or \> 35 kg/m².
  • Presence of any chronic medical condition other than overweight/obesity.
  • Known cardiovascular, metabolic, respiratory, or musculoskeletal disease that contraindicates high-intensity exercise.
  • Pregnancy.
  • Inability to perform exercise testing or complete the WB-HIIT program.
  • Any condition judged by investigators to interfere with participation or data interpretation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Université libre de Bruxelles (ULB)

Brussels, Belgium

RECRUITING

Related Publications (2)

  • Scoubeau C, Bonnechere B, Cnop M, Faoro V, Klass M. Effectiveness of Whole-Body High-Intensity Interval Training on Health-Related Fitness: A Systematic Review and Meta-Analysis. Int J Environ Res Public Health. 2022 Aug 3;19(15):9559. doi: 10.3390/ijerph19159559.

    PMID: 35954911BACKGROUND
  • Scoubeau C, Carpentier J, Baudry S, Faoro V, Klass M. Body composition, cardiorespiratory fitness, and neuromuscular adaptations induced by a home-based whole-body high intensity interval training. J Exerc Sci Fit. 2023 Apr;21(2):226-236. doi: 10.1016/j.jesf.2023.02.004. Epub 2023 Mar 10.

    PMID: 36970125BACKGROUND

MeSH Terms

Conditions

Overweight

Condition Hierarchy (Ancestors)

OvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Malgorzata Klass, PhD; Prof.

    Université libre de Bruxelles (ULB), Research Unit in Cardio-respiratory Physiology, Exercise & Nutrition

    STUDY DIRECTOR

Central Study Contacts

Julie Carpentier, PhD

CONTACT

Malgorzata Klass, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: Participants are allocated into two parallel groups (intervention vs. control) using semi-stratified assignment based on age, BMI, and sex to balance baseline characteristics. The intervention group completes a supervised 10-week WB-HIIT program, while the control group maintains usual lifestyle habits. All participants undergo identical pre- and post-intervention assessments.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 19, 2026

First Posted

May 13, 2026

Study Start

November 9, 2022

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

May 13, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared due to confidentiality requirements and restrictions imposed by the ethics committee.

Locations