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COMPLETED
NCT07787910
NA

Effect of Virtual Reality on Agitation in Acute Stroke

Sponsor: Ankara Etlik City Hospital

View on ClinicalTrials.gov

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

Interventions

BEHAVIORAL

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.

OTHER

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)