Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06441422

Blood Flow Restriction Training for People With Disabilities

Led by Medical College of Wisconsin · Updated on 2026-05-01

24

Participants Needed

1

Research Sites

159 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A large portion of the American population live with disabilities. People with disabilities can find it difficult to perform standard exercise routines. Regular exercise is necessary to be healthy, especially as people age. Lack of exercise can lead to secondary health concerns, like loss of muscle mass, diabetes, heart attack or stroke, to name a few. For exercise to be most beneficial, a certain degree of intensity must be achieved. Low load blood flow restriction training may be able to mimic the intensity of beneficial exercise without actually exercising hard. It may be a good option for people with disabilities who find it difficult to exercise.

CONDITIONS

Official Title

Blood Flow Restriction Training for People With Disabilities

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • Age �3E= 18
  • English speaking
  • Able to understand and perform upper extremity exercises
Not Eligible

You will not qualify if you...

  • Pregnant
  • Body mass index >40 kg�b7m-2
  • Uncontrolled hypertension (>150/90 mmHg)
  • Presence of neuromuscular junction and other muscle diseases
  • Myocardial infarction in the past 6 months
  • Unstable cardiovascular disease
  • History of an upper limb deep vein thrombosis
  • History of autonomic dysreflexia
  • Upper extremity fracture within the last 6 months

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical College of Wisconsin

Milwaukee, Wisconsin, United States, 53226

Actively Recruiting

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Research Team

B

Beth Weinman, DO

CONTACT

M

Meghann Sytsma

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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