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Effect of Virtual Reality on Agitation in Acute Stroke
Sponsor: Ankara Etlik City Hospital
Summary
This randomized controlled, single-blind study evaluates the effect of a Virtual Reality (VR) application on agitation levels and physiological vital signs in patients with acute stroke. Participants are randomly assigned to an intervention group receiving standard clinical care plus structured VR sessions, or a control group receiving standard clinical care alone. Agitation scores and vital signs (heart rate, blood pressure, respiratory rate, and oxygen saturation) are measured pre- and post-intervention to evaluate the outcomes of VR therapy.
Official title: The Effect of Virtual Reality Application on Agitation in Individuals With Acute Stroke: A Randomized Controlled Single-Blind Study
Key Details
Gender
All
Age Range
18 Years - 90 Years
Study Type
INTERVENTIONAL
Enrollment
68
Start Date
2025-09-08
Completion Date
2026-06-20
Last Updated
2026-08-26
Healthy Volunteers
No
Conditions
Interventions
Virtual Reality Application
Participants receive structured Virtual Reality (VR) relaxation and distraction sessions in addition to standard clinical stroke care to manage post-stroke agitation.
Standard Care (in control arm)
Participants receive routine standard clinical stroke care and monitoring alone without any Virtual Reality intervention.
Locations (1)
Çankırı Karatekin University
Ankara, Turkey (Türkiye)