ClinicalTrials.Veeva

Menu

Blood Flow Restriction for Optimizing Balance in Parkinson's Disease

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Enrolling

Conditions

Parkinson's Disease and Parkinsonism

Treatments

Other: Instability Resistance Training
Other: Blood flow restriction training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06508801
P30AG044271
STUDY00000472BFR

Details and patient eligibility

About

This study is being done to understand how reducing blood flow (BRT) during balance-challenging strengthening exercises (instability resistance training, or IRT) can help improve symptoms of Parkinson's disease.

Full description

Parkinson's disease (PD) is a disease of the nervous system that attacks the nerve cells in the brain responsible for controlling movement in the arms, legs and face. It is a progressive condition that gets worse with time. The purpose of this study is to determine the effects of blood flow restriction (BFR) in combination with strengthening exercises that challenge balance (instability resistance training (IRT)) to improve the symptoms of the participant's condition. This research is being done to understand the effects of BFR with IRT on symptoms of PD such as balance, mobility, walking and endurance. There will be two groups 1 and 2; group 1 will perform IRT with BFR and group 2 will perform IRT only. Each session with either intervention will last approximately 45 minutes. Researchers will test the effects of the intervention on the participant's walking ability, balance function and endurance. The researchers hope to learn whether low resistance exercises using these tight cuffs around the thighs are well tolerated by individuals with PD and determine whether there is an improvement in muscle strength, balance, and physical function. In addition, researchers will also use peripheral nerve stimulation techniques which are non-invasive (does not go inside the body). These techniques will be used to measure spinal excitability (i.e., nerve stimulator for testing strength of the pathway between spinal cord and muscles) in individuals with PD.

Enrollment

20 estimated patients

Sex

All

Ages

40 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Males and females between the ages 40 - 85 with a diagnosis of idiopathic Parkinson's Disease (PD) consistent with the United Kingdom PD society brain bank criteria,
  2. in Hoehn and Yahr stage 2-4,
  3. a score of ≥23 on the mini-Mental Scale Examination.

Exclusion criteria

  1. History of cardiovascular disease, uncontrolled hypertension (blood pressure ≥140/90 mmHg), orthostatic hypotension, deep-vein thrombosis, varicose veins, or rhabdomyolysis;
  2. Ankle branchial index ≤ 0.9 or > 1.3.
  3. History of other neurological disorders affecting the central nervous system such as stroke, multiple sclerosis, tumors, amyotrophic lateral sclerosis or muscle disease such as muscular dystrophy, myopathy.
  4. History of uncontrolled diabetes, severe osteoporosis, or cognitive impairment.
  5. Body mass index above 40; such individuals are more likely to have poorer muscle function and more pain.
  6. Absolute contraindications to exercise as per the American College of Sports Medicine (uncontrolled arrhythmias, third-degree heart block, recent electrocardiogram (EKG) changes, unstable angina, acute myocardial infarction, or acute congestive heart failure
  7. Had surgery in the lower extremities within the past 6 months.
  8. Pre-menopausal and not on birth control
  9. Pregnant or planning to become pregnant within the course of the study
  10. Plan to have major surgery within 2 months.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 2 patient groups

BFR plus IRT Group
Experimental group
Description:
Blood Flow Restriction plus Instability Resistance Training group. Participants will receive 2 sessions per week over 6 weeks.
Treatment:
Other: Blood flow restriction training
Other: Instability Resistance Training
IRT Only Control Group
Other group
Description:
Instability Resistance Training only group. Participants will receive 2 sessions per week over 6 weeks.
Treatment:
Other: Instability Resistance Training

Trial contacts and locations

1

Loading...

Central trial contact

Alyssa Main; Anjali Sivaramakrishnan, PhD, PT

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems