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Effect of Virtual Reality on Agitation in Acute Stroke

NCT07787910 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2026-08-26

No results posted yet for this study

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.

Conditions

  • Acute Stroke
  • Psychomotor Agitation

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.

Sponsors & Collaborators

  • Çankırı Karatekin University

    collaborator OTHER

  • Ankara Etlik City Hospital

    lead OTHER_GOV

Principal Investigators

  • Seher Gönen Şentürk, PhD · Çankırı Karatekin University, Faculty of Health Sciences

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-08
Primary Completion
2026-06-16
Completion
2026-06-20

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07787910 on ClinicalTrials.gov