- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07628478
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Pangfeng Liu Liu
- Phone Number: 18569427353
- Email: 965004077@qq.com
Study Locations
-
-
Changsha
-
Changsha, Changsha, China, 410073
- Recruiting
- Physical Training Hall
-
Contact:
- Pangfeng Liu Liu
- Phone Number: 18569427353
- Email: 965004077@qq.com
-
-
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.
Clinical Trials on Body Composition
-
Efforia, IncRecruiting
-
Dynamical Business and Science Society - DBSS International...Universidad de Córdoba; CES University; ARTHROS Centro de Fisioterapia y EjercicioRecruiting
-
Nova Southeastern UniversityCompleted
-
Centro Universitario de Ciencias de la Salud, MexicoCompleted
-
University of Southern CaliforniaCompleted
-
University of California, San FranciscoHologic, Inc.Completed
-
University of SurreyUnknownBody Composition
-
Texas Woman's UniversityCompleted
-
Efforia, IncRecruiting
-
Efforia, IncRecruiting
Clinical Trials on KAATSU Master Pneumatic Cuff
-
Seoul National University HospitalAsan Medical CenterCompletedCardiac Surgical Procedures | Myocardium; InjuryKorea, Republic of
-
Seoul National University HospitalCompletedIschemic Heart DiseaseKorea, Republic of
-
Poitiers University HospitalCompletedVentilation-associated Pneumonia | Severe Trauma PatientFrance
-
University Hospital, LilleCompletedContinuous Control of Polyurethane Tracheal-cuff Pressure: Efficiency of a Pneumatic Device (Nosten)Mechanical Ventilation Complication | Tracheal Intubation MorbidityFrance
-
University GhentFund for Scientific Research, Flanders, BelgiumCompleted
-
University Hospital, GhentFund for Scientific Research, Flanders, BelgiumCompletedBlood Flow RestrictionBelgium
-
University Hospital, GhentRecruitingAchilles Tendon Rupture | Blood Flow Restriction TherapyBelgium
-
The University of Texas Medical Branch, GalvestonNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)Completed
-
Riphah International UniversityNot yet recruiting