Effectiveness of Immersive Virtual Reality (IVR) Combined With Task-Specific Training on Hemiplegic Arm Function Following Stroke: A Single Case Series Study.

Virginia Commonwealth University1 site in 1 country13 target enrollmentMarch 12, 2023

ConditionsStroke

InterventionsVR immersive therapy

Overview

Phase: Not Applicable
Intervention: VR immersive therapy
Conditions: Stroke
Sponsor: Virginia Commonwealth University
Enrollment: 13
Locations: 1
Primary Endpoint: Change in hemiplegic arm movements
Status: Completed
Last Updated: last month

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this research study is to understand the efficacy of using an immersive Virtual Reality (VR) environment, with task-specific training, to encourage arm movement following stroke.

Detailed Description

The study will investigate how people who have had a stroke use their weakened arm in everyday tasks, and how this relates to measurements of movement ability from standardized clinic tests. Results of this research will ultimately help develop more effective training approaches to be used with stroke survivors.

Registry

clinicaltrials.gov

Start Date

March 12, 2023

End Date

November 20, 2025

Last Updated

last month

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Virginia Commonwealth University

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Age 18 or older.
•Diagnosed as having an ischemic or hemorrhagic stroke (with documented confirmatory neuroimaging in the medical record) that occurred at least 6-months prior to study enrollment.
•Lack of full active range of motion in the involved shoulder, elbow, and wrist as the result of the injury.
•At the time of study enrollment, participant completed structured therapeutic interventions at least 2-months prior.
•Participants will not participate in Yoga, Tai-Chi, or other wellness lifestyle classes while participating in the study.
•Absence of significant cognitive impairment as determined by a Mini-Mental Status Examination score of greater than or equal to
•The absence of upper extremity injury limiting functional use of the arm prior to the incident stroke.

Exclusion Criteria

•Unable to provide informed consent.
•Sensory loss as determined by a score of 2 on the sensory item of the NIH Stroke Scale.
•Pain in the involved upper limb that could interfere with daily activities as evidenced by a pain score of 5 or greater on the Numeric Pain Rating Scale.
•History of greater than two strokes.
•Suffered a stroke less than 6-months prior to participating in the study.
•A history of, or being susceptible to, cyber-sickness (i.e., motion sickness).
•Unable to don/doff accelerometer independently, or the lack of support in the home to assist with donning/doffing device; and
•A history of seizures.