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Clinical Trials/NCT03540147
NCT03540147
Terminated
Not Applicable

The Impact of Blood Flow Restriction (BFR) on Exercise and Hemodynamic Responses

University of Texas at Austin1 site in 1 country20 target enrollmentJanuary 26, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Exercise Training
Sponsor
University of Texas at Austin
Enrollment
20
Locations
1
Primary Endpoint
Flow-mediated Dilation
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

The impact of blood flow restriction (BFR) on exercise and hemodynamic responses will be studied. The use of BFR will be studied during yoga and low-intensity aerobic exercise in healthy subjects with no history of chronic illness ranging from 18-40 years of age. This study will evaluate several conditions related to cardiovascular physiology in order to determine the safety and efficacy of this type of exercise training. First, the effects of two distinct types of BFR cuffs (BStrong and Hokanson) will be studied during low-intensity aerobic exercise on vascular function. Second, the effect of yoga will be studied with and without the use of BStrong bands on vascular function. Outcome measures include acute effects on endothelial function i.e. flow-mediated dilation, arterial stiffness, beat-by-beat blood pressure, heart rate, RPE (rate of perceived exertion), and blood lactate. For this intervention, the BFR cuffs will be used during exercise to evaluate its safety and efficacy. Since BFR is becoming a widely popular method of exercise, it is important to study its safety and hemodynamic effects.

Detailed Description

Participants will be tested a total of 5 times; twice for the yoga portion and thrice for the aerobic exercise (walking) portion. Outcome measures will be consistent across the five visits and will take approximately 2.5 hours to complete. The order of the five separate sessions will be randomized such that the participant cannot expect which condition they will be performing.

Registry
clinicaltrials.gov
Start Date
January 26, 2018
End Date
May 26, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hirofumi Tanaka

Professor

University of Texas at Austin

Eligibility Criteria

Inclusion Criteria

  • Healthy adults

Exclusion Criteria

  • Pregnancy
  • A recent illness, recent surgery, or any medical intervention
  • history of diabetes, heart disease, or other cardiovascular problems

Outcomes

Primary Outcomes

Flow-mediated Dilation

Time Frame: Before (baseline) and after the exercise interventions

After 20 minutes of supine rest, endothelial function was measured via flow-mediated dilation (FMD) technique by measuring the brachial artery's diameter increase following a brief period of occlusion using an automated diagnostic ultrasound system. A blood pressure cuff was placed on the forearm with the proximal edge of the cuff above with the participant's antecubital fossa. Two cross-sectional images of the artery were acquired utilizing the automated ultrasound probe proximal to the antecubital fossa. Following baseline metrics, the cuff was inflated to 50 mmHg above resting systolic blood pressure for 5 minutes to occlude blood flow. After 5 minutes of occlusion, the cuff was deflated, and both brachial artery diameter and blood flow velocity were measured simultaneously and continuously for two-minutes immediately post occlusion. FMD was calculated as a percent increase in brachial artery diameter at the post-blood flow occlusion compared with the pre-blood flow occlusion.

Systolic Blood Pressure

Time Frame: Measurements were taken at Baseline (before Experimental Arm Participation) and immediately after Experimental Arm Participation.

Arterial blood pressure was measured using the automatic oscillometric methods.

Study Sites (1)

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