MedPath

Virtual Reality in End Stage Kidney Disease

Not Applicable
Not yet recruiting
Conditions
End Stage Kidney Disease
Interventions
Behavioral: Individual Virtual Reality
Behavioral: Social Virtual Reality
Registration Number
NCT06356168
Lead Sponsor
University of Pennsylvania
Brief Summary

The goal of this clinical trial to compare the social virtual reality and individual virtual reality in patients with end stage kidney disease who are hemodialysis. The main aim is to determine if there are differences in symptoms between the groups. Participants will use virtual reality glasses for 30-45 minutes during dialysis sessions for 4 weeks.

Detailed Description

In a single site, 2-arm (Social Virtual Reality group; Individual Virtual Reality Group), parallel, randomized controlled trial we will enroll 60 subjects (n=30 per group) to assess the effects of Social Virtual Reality to Individual Virtual Reality on symptoms in participants with end stage kidney disease who are receiving hemodialysis.

To compare the effects of social virtual reality to individual virtual reality on loneliness To explore the effects of social virtual reality to individual virtual reality on anxiety and depression.

To compare the effects social virtual reality to individual virtual reality on quality of life.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Individual Virtual RealityIndividual Virtual RealityIndividual Virtual Reality will be delivered using virtual reality glasses for 30-45 minutes during dialysis sessions. Those randomized to this arm will watch a movie or program alone through the glasses.
Social Virtual RealitySocial Virtual RealitySocial Virtual Reality will be delivered using virtual reality glasses for 30-45 minutes during dialysis sessions. Groups of 3 participants will watch a movie or program together through the glasses. They will be able to talk and interact during the session.
Primary Outcome Measures
NameTimeMethod
De Jong Gierveld ScaleBaseline and 4 Weeks

Measures how bad or severe a person's loneliness is. Score range from 11-44; higher scores indicate more loneliness.

Secondary Outcome Measures
NameTimeMethod
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