RECRUITING

Virtual Reality Based Rehabilitation After Ischemic Stroke

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

Use the template below as a guide to write a brief study description in plain language. Tailor the text that appears in brackets and yellow to your research study. To finalize, delete the text in italics. The goal of this single-arm study is to explore the use of early virtual reality-based rehabilitation as an adjunct to conventional physical/occupational therapy in adult patients with acute ischemic stroke. The main question it aims to answer is: Feasibility and tolerability of using immersive Virtual Reality technology-based therapy for patients suffering from acute ischemic stroke in an inpatient hospital setting Participants will receive 1 or 2 virtual reality therapy sessions and complete surveys at the end of each session.

Official Title

Improving Functional and Cognitive Outcomes After Ischemic Stroke Using Virtual Reality Based Rehabilitation

Quick Facts

Study Start:2023-04-17
Study Completion:2026-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06401564

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age \> 18
  2. * MRI or CT imaging confirmed ischemic stroke
  3. * Able to follow multistep commands
  1. * Plegia in both arms
  2. * Previous reported history of vertigo or inner ear dysfunction
  3. * Patients with epilepsy
  4. * Patients who cannot begin therapy during admission
  5. * Patients who are pregnant
  6. * Patients with a pre-existing condition that interferes with virtual reality usage (e.g., visual impairment, limitation of either upper extremity or neck).

Contacts and Locations

Study Contact

Christine Pol, PhD
CONTACT
(631) 444-9083
christiana.pol@stonybrookmedicine.edu
Ruth Reinsel, PhD
CONTACT
(631) 638-2087
ruth.reinsel@stonybrookmedicine.edu

Principal Investigator

Jason Mathew, DO
PRINCIPAL_INVESTIGATOR
Stony Brook University Hospital

Study Locations (Sites)

Stony Brook University Hospital
Stony Brook, New York, 11794-8121
United States

Collaborators and Investigators

Sponsor: Stony Brook University

  • Jason Mathew, DO, PRINCIPAL_INVESTIGATOR, Stony Brook University Hospital

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 Date2023-04-17
Study Completion Date2026-12

Study Record Updates

Study Start Date2023-04-17
Study Completion Date2026-12

Terms related to this study

Keywords Provided by Researchers

  • virtual reality
  • stroke rehabilitation
  • quality of life
  • upper extremity

Additional Relevant MeSH Terms

  • Ischemic Stroke