RECRUITING

Endurance Exercise & Virtual Reality for Optimizing Cortical Excitability and Neuroplasticity in PD

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study aims to determine the effects of aerobic exercise as a primer to add-on virtual reality (VR)-based rehabilitation on balance, postural control and neuroplasticity (ability of brain to adapt in structure and function) in individuals with Parkinson's disease (PD). This study will utilize two groups - one group will receive the exercise and VR, while the other group will receive stretching exercise and VR over eight weeks. The study team will administer outcomes at baseline, post-intervention (8 weeks) and follow-up (6 weeks after post-assessment).

Official Title

High Intensity Endurance Exercise as a Primer to Virtual Reality for Optimizing Cortical Excitability and Neuroplasticity in Parkinson's Disease (PD)

Quick Facts

Study Start:2024-02-09
Study Completion:2025-04-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06133283

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Diagnosis of idiopathic PD (ages 18 -85) in Hoehn and Yahr stages 2 - 3.
  2. 2. Subjects need to demonstrate a score of equal to or greater than 23 on the Mini Mental State Examination.
  3. 3. Subjects who have a score of ≤21.5 on the Mini Balance Evaluations Systems Test (miniBESTest).
  1. 1. Subjects with a history of other neurological diseases (i.e., stroke, multiple sclerosis).
  2. 2. Subjects with a history of severe cardiopulmonary disease, uncontrolled hypertension, orthostatic hypotension, uncontrolled diabetes, severe osteoporosis, severe arthritis affecting their lower extremity joints.
  3. 3. Subjects with a history of PD-specific surgical procedures such as deep brain stimulation etc.
  4. 4. Subjects with a history of head injury.
  5. 5. Subjects with a history of seizures or epilepsy.
  6. 6. Subjects who are currently pregnant.
  7. 7. Individuals who use of medications that could alter corticomotor excitability or increase risk of seizure.
  8. 8. Individuals with skull abnormalities, fractures or unexplained, recurring headaches.

Contacts and Locations

Study Contact

Anjali Sivaramakrishnan, PhD
CONTACT
210-567-8626
sivaramakris@uthscsa.edu

Principal Investigator

Anjali Sivaramakrishnan
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center at San Antonio

Study Locations (Sites)

UT Health San Antonio- Dept. of Physical Therapy
San Antonio, Texas, 78229
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center at San Antonio

  • Anjali Sivaramakrishnan, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center at San Antonio

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-09
Study Completion Date2025-04-30

Study Record Updates

Study Start Date2024-02-09
Study Completion Date2025-04-30

Terms related to this study

Keywords Provided by Researchers

  • Aerobic exercise
  • Virtual reality
  • Rehabilitation
  • Balance
  • Neurophysiology

Additional Relevant MeSH Terms

  • Parkinson Disease