Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06401564

Virtual Reality Based Rehabilitation After Ischemic Stroke

Led by Stony Brook University · Updated on 2024-05-06

15

Participants Needed

1

Research Sites

189 weeks

Total Duration

On this page

Sponsors

S

Stony Brook University

Lead Sponsor

G

Good Samaritan Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Virtual Reality Based Rehabilitation After Ischemic Stroke

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18
  • Ischemic stroke confirmed by MRI or CT imaging
  • Able to follow multistep commands
Not Eligible

You will not qualify if you...

  • Paralysis in both arms
  • History of vertigo or inner ear dysfunction
  • Epilepsy
  • Unable to start therapy during hospital admission
  • Pregnancy
  • Pre-existing conditions affecting virtual reality use, such as visual impairment or limitations in upper extremity or neck

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

Stony Brook University Hospital

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

Actively Recruiting

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Research Team

C

Christine Pol, PhD

CONTACT

R

Ruth Reinsel, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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