MedPath

The Influences of Single Chamber vs. Multi-chamber Blood Flow Restriction Cuffs

Not Applicable
Active, not recruiting
Conditions
Blood Vessel Disease
Muscle Edema
Registration Number
NCT06276673
Lead Sponsor
Salisbury University
Brief Summary

The purpose of this study is to investigate the use of single (SC) and multi-chamber (MC) blood flow restriction (BFR) cuff exercise on indices of arterial stiffness, muscle morphology, and participant perception.

Detailed Description

Thirty adults aged 18-40 years old will undergo three treatment sessions (control (no BFR), SC BFR, and MC BFR) in a randomized order separated by one week. A familiarization session will also occur one week before starting the treatment period. Each subject will undergo a series of tests including anthropometry, ultrasonography of the carotid artery, applanation tonometry, ultrasonography of the vastus lateralis, blood pressure acquisition, body composition, and maximal strength assessments (1RM). The exercise trial will consist of sets of dumbbell wall squats performed to failure with a 2-seconds concentric and 2-seconds eccentric cadence, at 20% of their 1RM using 60% of the supine limb occlusion pressure (LOP) with 1-minute rest intervals. Assessments will be performed immediately before and after the exercise bout during each treatment session. Two-way ANOVAs will be used to examine the main effects of treatment and treatment-order interaction on pulse wave velocity, muscle cross-sectional area, and perceptual response.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
35
Inclusion Criteria
  1. Physically active (> 1,000 MET/min/wk) for at least six months.
  2. Weight stable for previous 6 months (+/-2.5 kg)
  3. Female subjects only- reported regular menstrual cycles for the last 2 years
Exclusion Criteria
  1. BP>140/90 mmHg
  2. BMI>40 kg/m2
  3. Diabetes
  4. Familial hypercholesterolemia
  5. Past or current history of CHD, stroke or major CVD events. Respiratory diseases (not including asthma), endocrine or metabolic, neurological, or hematological disorders that would compromise the study or the health of the subject.
  6. Women must not be pregnant, plan to become pregnant during the study, or be nursing
  7. Active renal or liver disease
  8. All medications and supplements that influence dependent variables*
  9. Recent surgery < 2 months
  10. Alcohol abuse
  11. Sleep apnea
  12. Claustrophobia

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Muscle MorphologyPrior to and immediately after the exercise intervention

A measurement of vastus lateralis cross sectional area

Arterial StiffnessPrior to and 10-minutes after the exercise intervention

A measurement of vascular health.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Salisbury University

🇺🇸

Salisbury, Maryland, United States

Salisbury University
🇺🇸Salisbury, Maryland, United States

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.