NCT05835557

Brief Summary

This research study revolves around the physiological outcomes of using post-exercise blood flow restriction (BFR) with high intensity short interval training (ST) The main aims of this study are to compare (i) aerobic performance outcomes, and (ii) anaerobic and muscular performance outcomes - between 2 groups of participants after either undergoing 3 weeks of ST + post-exercise BFR (BFR-ST) or traditional ST.

Trial Health

87
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
Completed

Started Jul 2023

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 5, 2023

Completed
23 days until next milestone

First Posted

Study publicly available on registry

April 28, 2023

Completed
2 months until next milestone

Study Start

First participant enrolled

July 1, 2023

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2024

Completed
Last Updated

April 13, 2025

Status Verified

April 1, 2025

Enrollment Period

1.3 years

First QC Date

April 5, 2023

Last Update Submit

April 10, 2025

Conditions

Outcome Measures

Primary Outcomes (3)

  • Maximum oxygen uptake and power

    Will be assessed at baseline (Day 0 - Pre) and the change in this outcome 24 hours after 9 sessions of training over 3 weeks (Post)

  • 20 km Cycling time trial

    Will be assessed at baseline (Day 0 - Pre) and the change in this outcome 24 hours after 9 sessions of training over 3 weeks (Post)

  • Wingate test of anaerobic power

    Peak and mean power and rate of fatigue

    Will be assessed at baseline (Day 0 - Pre) and the change in this outcome 24 hours after 9 sessions of training over 3 weeks (Post)

Secondary Outcomes (3)

  • Exercise economy

    Will be assessed at baseline (Day 0 - Pre) and the change in this outcome 24 hours after 9 sessions of training over 3 weeks (Post)

  • Isometric mid-thigh pull

    Will be assessed at baseline (Day 0 - Pre) and the change in this outcome 24 hours after 9 sessions of training over 3 weeks (Post)

  • Countermovement jump height

    Will be assessed at baseline (Day 0 - Pre) and the change in this outcome 24 hours after 9 sessions of training over 3 weeks (Post)

Study Arms (2)

Blood flow restriction with short interval training (BFR-ST)

EXPERIMENTAL

9 sessions of high intensity short interval training with blood flow restriction.

Other: BFR-ST

Sham altitude with short interval training (ST)

SHAM COMPARATOR

9 sessions of high intensity short interval training in an altitude chamber.

Other: ST

Interventions

BFR-STOTHER

Undergo 9 sessions of high intensity short interval training involving 3 sets of 8-10 repetitions of 30 secs interval cycling and 30 secs recovery at 100-110% of maximal aerobic power. In between sets there will be 3 mins of passive rest. Blood flow restriction will be applied for 2 mins during the passive rest at 80% of limb occlusion pressure.

Blood flow restriction with short interval training (BFR-ST)
STOTHER

Undergo 9 sessions of high intensity short interval training involving 3 sets of 8-10 repetitions of 30 secs interval cycling and 30 secs recovery at 100-110% of maximal aerobic power. In between sets there will be 3 mins of passive rest. Cycling will be conducted in an environmental chamber and participants informed that the altitude is set to 2500m - actual altitude will be sea level.

Sham altitude with short interval training (ST)

Eligibility Criteria

Age18 Years - 40 Years
Sexmale(Gender-based eligibility)
Gender Eligibility DetailsMales
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Male
  • years
  • Actively performing endurance exercise (running or cycling) for at least 2 sessions (1 - 1.5h) per week
  • Healthy (free from illnesses) and no musculoskeletal injuries for the past 6 months
  • No history of cardiometabolic, vascular diseases or similar conditions (e.g., high blood pressure, peripheral vascular diseases, heart diseases, metabolic syndrome, diabetes, stroke, etc.).
  • Pass the pre-participation health screening tests - Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) and Australian Institute of Sport Blood Flow Restriction (AIS BFR) pre-screening questionnaire (no history of any risk factors).
  • Achieve a maximum oxygen uptake (VO2max) of ≥40ml/kg/min during a maximal aerobic power cycling screening test.
  • Non-smoker
  • Drink alcohol less than 3 times each week and less than 3 drinks each time

You may not qualify if:

  • Persons with any form of illnesses and/or musculoskeletal injuries for the past 6 months
  • Any history of cardiometabolic, vascular diseases or similar conditions which may worsen with the use of blood flow restriction during exercise
  • Fail the pre-participation health screening tests
  • Below 40ml/kg/min VO2max during maximal aerobic power cycling test
  • Smoker
  • History of asthma or taking medication for asthma.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Human Bioenergetics Laboratory, National Institute of Education, Nanyang Technological University

Singapore, 637616, Singapore

Location

Related Publications (1)

  • Chua MT, Sim A, Aziz AR, Polglaze T, Burns SF. Blood Flow Restriction during Rest Periods of High-Intensity Interval Training Enhances Endurance Performance: A Randomized Placebo-Controlled Study. Med Sci Sports Exerc. 2026 Jan 1;58(1):86-98. doi: 10.1249/MSS.0000000000003834. Epub 2025 Aug 12.

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Masking Details
Sham treatment of altitude exposure in an environmental chamber.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Two groups exposed to 9 sessions of high intensity short interval training with or without blood flow restriction between sets of exercise.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

April 5, 2023

First Posted

April 28, 2023

Study Start

July 1, 2023

Primary Completion

September 30, 2024

Study Completion

September 30, 2024

Last Updated

April 13, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will share

All published data will be placed into the Data Repository of Nanyang Technological University National Institute of Education for public access upon publication.

Shared Documents
ANALYTIC CODE
Time Frame
Upon publication - permanent repository
Access Criteria
Public repository - exact web address available upon publication.
More information

Locations