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Cardiovascular Response to Isometric BFR Exercise

Blood Pressure Responses to Isometric Blood Flow Restriction Exercise

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06529068
Enrollment
21
Registered
2024-07-31
Start date
2024-12-02
Completion date
2025-05-30
Last updated
2026-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure

Brief summary

The goal of this interventional study is to evaluate the acute impact of isometric blood flow restriction (BFR) exercise on blood pressure and other cardiovascular functions in healthy young adult volunteers. The main question it aims to answer is: The investigators hypothesize that isometric BFR exercise with a wide-rigid cuff would lead to greater blood pressure and other cardiovascular responses and that these cardiovascular responses would be greater under isometric BFR exercise with narrow-elastic bands compared with the control condition (no cuff). Participants will perform isometric exercises in 3 laboratory visits with different exercise conditions) no cuff control 2) BFR with wide-rigid cuff 3) BFR with narrow-elastic band.

Interventions

The participants will perform isometric handgrip exercises without blood flow restriction.

BEHAVIORALIsometric handgrip exercise with a narrow-elastic band

The participants will perform isometric handgrip exercises with blood flow restriction using a narrow-elastic band.

BEHAVIORALIsometric handgrip exercise with a wide-rigid cuff

The participants will perform isometric handgrip exercises with blood flow restriction using a wide-rigid cuff.

Sponsors

Hirofumi Tanaka
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

\- Apparently healthy young adults aged between 18 - 40 years old and signed the informed consent.

Exclusion criteria

* Abnormal clotting times * Acid-base imbalance/acidosis * Arterial calcification * Atherosclerotic vessels * Cardiopulmonary conditions * Diabetes * Dialysis/central venous access * General/local infection * High intracranial pressure * Hip, pelvis, or femur fracture * History of venous thromboembolism * Hypertension * Immobility for greater than 48 hours in the past month * Immobilizing cast * Implanted medical device * Lymphectomies * Obesity * Open fracture * Open or unhealed soft tissue injuries * Paralysis * Peripheral vascular disease * Pregnancy/postpartum * Prior revascularization * Renal compromise * Severe crush injuries * Sickle cell trait/anemia * Skin grafts * Stroke * Temporary nerve damage * Thrombophilia * Tumor/cancer * Varicose veins * Vascular grafting

Design outcomes

Primary

MeasureTime frameDescription
Systolic blood pressure and diastolic blood pressure20 minutesBeat-by-beat (both systolic and diastolic blood pressure) blood pressure before, during, and after exercise
Brachial artery diameter evaluated by an ultrasound machineBefore and 20 minutes after exerciseBrachial artery diameter will be measured by an ultrasound machine to calculate flow-mediated dilation (FMD)
Heart rate20 minutesMonitor heart rate continuously before, during, and after exercise

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 11, 2026