CompletedNot Applicable

The Feasibility, Usability, and Acceptability of Using the Oculus™ Virtual Reality Gaming Technology in Stroke Survivors for Upper Extremity and Cognitive Rehabilitation

United States32 participantsStarted 2023-03-05

Plain-language summary

The purpose of this study is to test the (a) feasibility, (b) usability, and (c) acceptability of using the Oculus Virtual Reality (VR) for chronic stroke survivors who have mild-moderate cognitive and unilateral arm impairment to administer upper extremity and cognitive rehabilitation, to calculate the change in upper extremity and cognition scores on standardized measurements per standard of care and to qualitatively explore the impact of engaging caregivers in supporting the stroke survivor's rehabilitation and the impact of this engagement on the stroke survivor and caregiver dyad using semi-structured interviews.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Ischemic or hemorrhagic stroke diagnosis within 6 months to 2 years of enrollment * can read, write, comprehend, speak English * willing and able to provide informed consent * Caregivers must live in the home with the stroke survivor Exclusion Criteria: * do not have score ranges that indicate mild to moderate severity on the Montreal Cognitive Assessment (MoCA )(15-25) or other appropriate cognitive screening test selected by the speech language pathologist * has aphasia, hemiopsia, and other neurological deficits that prevents the participant from being examined using MoCA or a modified MoCA, Fugl-Meyer Assessment - Upper Extremity (FM) (20-50) * unstable while standing unassisted * have a history of motion sickness/ vertigo/ dizziness/seizures, claustrophobia, blind/deaf, and cannot hold the controller in their affected arm.

What they're measuring

Feasibility as Assessed by the Number of Sessions Attended

Timeframe: end of intervention( about 4 weeks from baseline)

Feasibility as Assessed by the Time Spent Using the Oculus VR

Timeframe: end of intervention( about 4 weeks from baseline)

Usability as Assessed by the Score on the System Usability Scale (SUS)

Timeframe: end of intervention( about 4 weeks from baseline)

Usability as Assessed by the Score on the Presence Questionnaire (PQ)

Timeframe: end of intervention( about 4 weeks from baseline)

Cognition as Assessed by the Montreal Cognitive Assessment (MoCA)

Timeframe: Baseline

Cognition as Assessed by the Montreal Cognitive Assessment (MoCA)

Timeframe: end of intervention (about 4 weeks from baseline)

Limb Function as Assessed by the Action Research Arm Test (ARAT)

Timeframe: Baseline

Trial details

NCT IDNCT05672628

SponsorThe University of Texas Health Science Center, Houston

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-07-17

Results submitted2025-07-30

View on ClinicalTrials.gov More Stroke trials