Physiological Outcomes of High-intensity Interval Training With Post-exercise Blood Flow Restriction

Sponsor
Nanyang Technological University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05835557
Collaborator
(none)
34
1
2
16
2.1

Study Details

Study Description

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.
Condition or Disease Intervention/Treatment Phase
  • Other: BFR-ST
  • Other: ST
N/A

Detailed Description

This research study revolves around the physiological outcomes of using post-exercise blood flow restriction (BFR) with high-intensity interval exercise training (HIIT), specifically high intensity short interval training (ST) protocol of 30s work, 30s rest, for the recreational endurance athlete. In previous research, it has been shown that using BFR during rest intervals of a ST protocol would elicit greater physiological stresses in terms of higher heart rate, greater muscle activation, reduced oxygenation within the muscle tissue during exercise, and increased blood lactate post-exercise as compared with the control condition. However, the physiological outcomes of this type of training method over a longer-term (9 sessions over 3 weeks) have not been explored. The main aims of this study is to compare the physiological outcomes, - (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 . The hypotheses for this study are: the BFR-ST group would experience a (i) greater improvement in maximal aerobic capacity, function and time trial performance and, (ii) greater improvement in anaerobic power and capacity as well as muscular strength and power, as compared with the ST group.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
34 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups exposed to 9 sessions of high intensity short interval training with or without blood flow restriction between sets of exercise.Two groups exposed to 9 sessions of high intensity short interval training with or without blood flow restriction between sets of exercise.
Masking:
Single (Participant)
Masking Description:
Sham treatment of altitude exposure in an environmental chamber.
Primary Purpose:
Other
Official Title:
Physiological Outcomes of High-intensity Interval Training With Post-exercise Blood Flow
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Sep 30, 2024
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Blood flow restriction with short interval training (BFR-ST)

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

Other: BFR-ST
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.

Sham Comparator: Sham altitude with short interval training (ST)

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

Other: ST
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.

Outcome Measures

Primary Outcome Measures

  1. 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)]

  2. 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)]

  3. Wingate test of anaerobic 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)]

    Peak and mean power and rate of fatigue

Secondary Outcome Measures

  1. 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)]

    Oxygen uptake at a fixed load of 50% of maximum aerobic power

  2. 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)]

    Maximal strength assessment of lower body

  3. 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)]

    Vertical jump height assessment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male

  • 18-40 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

Exclusion Criteria:
  • 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

  • Consumption of alcohol beyond that stated in the inclusion criteria.

  • History of asthma or taking medication for asthma.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Human Bioenergetics Laboratory, National Institute of Education, Nanyang Technological University Singapore Singapore 637616

Sponsors and Collaborators

  • Nanyang Technological University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Stephen Burns, Associate Professor, Nanyang Technological University
ClinicalTrials.gov Identifier:
NCT05835557
Other Study ID Numbers:
  • IRB-2023-235
First Posted:
Apr 28, 2023
Last Update Posted:
Apr 28, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 28, 2023