Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Using virtual reality to help recover from ischemic stroke

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

Run by Stony Brook University · NCT06401564 · Data updated 2026-11-12

This study is testing whether virtual reality therapy can help adults recovering from a stroke feel better when combined with regular physical and occupational therapy.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment15 (estimated)
SponsorStony Brook University
Academic / other
Locations1 site (Stony Brook, New York)
StatusRecruiting
StartedApril 17, 2023
Main results expectedDecember 2025
Study endsDecember 2026
Registry record updatedMay 6, 2024
Trial IDNCT06401564 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults over 18 who have experienced an ischemic stroke and can follow multistep commands.

Probably not a fit

Patients with plegia in both arms, severe pre-existing conditions, or those unable to start therapy during admission may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study explores the use of virtual reality-based rehabilitation as an additional therapy for adults recovering from acute ischemic stroke. Participants will engage in one or two virtual reality therapy sessions while receiving conventional physical and occupational therapy. The study aims to assess the feasibility and tolerability of this immersive technology in an inpatient hospital setting, with participants completing surveys after each session to provide feedback on their experience.

Why it matters

Potential benefit: If successful, this approach could enhance recovery outcomes and improve the quality of life for stroke patients.

How similar studies have gone: Other studies have shown promise in using virtual reality for rehabilitation, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age \> 18
* MRI or CT imaging confirmed ischemic stroke
* Able to follow multistep commands

Exclusion Criteria:

* Plegia in both arms
* Previous reported history of vertigo or inner ear dysfunction
* Patients with epilepsy
* Patients who cannot begin therapy during admission
* Patients who are pregnant
* Patients with a pre-existing condition that interferes with virtual reality usage (e.g., visual impairment, limitation of either upper extremity or neck).

Where it's running

  • Stony Brook University Hospital
    Stony Brook, New York, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Remote ischemic conditioning for post-stroke insomnia

    A 136-person, randomized study will test whether a non-invasive arm-cuff procedure done twice daily for 90 days can improve sleep after a first ischemic stroke in adults 18–80.

    Recruiting Sichuan Academy of Medical Sciences · Chengdu, Sichuan · NCT07874594

  • Ear-based nerve stimulation to help sleep after a stroke

    A device that delivers vagal nerve stimulation through the ear is tested to see if it helps stroke patients in rehab sleep better.

    Recruiting Casa Colina Hospital and Centers for Healthcare · Pomona, California · NCT07858656

  • Theta Burst Stimulation to Help Stroke Recovery (Upper and Lower Limbs)

    This trial tests whether applying theta burst stimulation to the motor cortex, in combination with standard rehabilitation, helps people over 45 who recently had a first ischemic stroke recover arm and leg movement.

    Recruiting Ankara Etlik City Hospital · Ankara, Yenimahalle · NCT07834333

  • Preventing another ischemic stroke with a smart bracelet and app

    This study tests whether a digital prevention program using a wearable and a mobile app can help people who recently had an ischemic stroke reduce the chance of another stroke and improve risk-factor control.

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  • Photon-counting CT to check intracranial stents

    This study tests whether ultra-high-resolution photon-counting CT can reliably visualize intracranial stents and detect in-stent restenosis during follow-up of patients with prior stents.

    Recruiting Chinese PLA General Hospital · Beijing, Beijing Municipality · NCT07769814

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.