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NCT05728866Completed

Effectiveness of IVR Combined With Task-Specific Training on Hemiplegic Arm Function Following Stroke

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

Source: ClinicalTrials.gov · Last updated 19 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
13 (actual)
First submitted
6 Feb 2023
Start date
12 Mar 2023
Primary completion date
20 Nov 2025
Lead sponsor
Virginia Commonwealth University
Diseases
Stroke
NCT number
NCT05728866

What you commit to

  • Study type: Interventional
  • Participants enrolled: 13
  • From 12 Mar 2023 to the primary completion date, 20 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Suffered a stroke less than 6-months prior to participating in the study.

Other illness

  • Sensory loss as determined by a score of 2 on the sensory item of the NIH Stroke Scale.
  • History of greater than two strokes.
  • A history of, or being susceptible to, cyber-sickness (i.e., motion sickness).
  • A history of seizures.

Other

  • Unable to provide informed consent.
  • 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.
  • Unable to don/doff accelerometer independently, or the lack of support in the home to assist with donning/doffing device; and

Who the study is looking for

  • 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 24.
  • The absence of upper extremity injury limiting functional use of the arm prior to the incident stroke.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Virginia Commonwealth University
Coordinator of this site? Confirm its status
RichmondUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.