Effects of Blood Flow Restriction Training on Body Composition and Maximal Strength in Military Personnel

June 4, 2026 updated by: Yang Liu

Effects of Blood Flow Restriction Training on Body Composition and Maximal Strength in Military Personnel: A Prospective Randomized Controlled Trial

This study aims to compare the effects of low-intensity blood flow restriction training combined with resistance training versus traditional high-intensity resistance training on body composition (skeletal muscle mass, body fat mass) and maximal strength (isometric mid-thigh pull, vertical jump, isometric squat pull) in male military academy cadets. The study lasts for 6 weeks and adopts a randomized parallel-group design.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

36

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Changsha
      • Changsha, Changsha, China, 410073
        • Recruiting
        • Physical Training Hall
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male cadets from military academy;
  • No contraindications to blood flow restriction training (no circulatory diseases, skin allergies);
  • Healthy and capable of high-intensity exercise;
  • Signed informed consent

Exclusion Criteria:

  • Major sports injury within 2 years (fracture, ligament tear, muscle/tendon rupture, habitual joint dislocation);
  • Cardiovascular or visceral organ diseases;
  • Other conditions unsuitable for training

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Low-Load Blood Flow Restistance Training (LL-BFR)
Participants perform low-load resistance training (30% 1RM) combined with blood flow restriction. Lower extremity exercises include squat, deadlift, weighted lunge, and resisted running. Pneumatic cuffs (KAATSU Master) are applied at the proximal thigh at 200 mmHg during exercise and rest intervals. Training: 1 set of 30 reps, followed by 3 sets of 15 reps; 60-second rest between sets; 3 days/week for 6 weeks.
Pneumatic pressure cuffs applied to the proximal thigh at 200 mmHg to achieve partial blood flow restriction during low-load resistance training (30% 1RM). Initial warm-up at 40 mmHg.
Active Comparator: Traditional High-Load Resistance Training (HL-RT)
Participants perform traditional high-load resistance training at 70% 1RM. Same exercises as experimental group: squat, deadlift, weighted lunge, and resisted running. 4 sets of 8-12 reps; 3-minute rest between sets; 3 days/week for 6 weeks.
Traditional resistance training at 70% of one-repetition maximum (1RM) without blood flow restriction.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Peak Force in Isometric Mid-Thigh Pull (IMTP)
Time Frame: Baseline (T1), Week 3 (T2), Week 6 (T3)
Maximal vertical ground reaction force during isometric mid-thigh pull measured on ELIGA portable force plate. Participants pull a fixed bar with knee angle 125°-135° for 3-5 seconds. Best of 2 trials recorded in Newtons (N).
Baseline (T1), Week 3 (T2), Week 6 (T3)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Countermovement Jump Height (CMJ)
Time Frame: Baseline (T1), Week 6 (T3)
Vertical jump height calculated from flight time measured on ELIGA portable force plate. Formula: height = g × t²/8, where g = 9.81 m/s². Hands on hips, self-selected countermovement depth. Best of 3 trials in centimeters (cm).
Baseline (T1), Week 6 (T3)
Body Fat Mass
Time Frame: Baseline (T1), Week 6 (T3)
Total body fat mass measured by bioelectrical impedance analysis (InBody). Expressed in kilograms (kg).
Baseline (T1), Week 6 (T3)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

July 20, 2026

Study Completion (Estimated)

July 28, 2026

Study Registration Dates

First Submitted

May 29, 2026

First Submitted That Met QC Criteria

June 4, 2026

First Posted (Actual)

June 5, 2026

Study Record Updates

Last Update Posted (Actual)

June 5, 2026

Last Update Submitted That Met QC Criteria

June 4, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 2026069

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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