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Tandem Virtual Reality Experience for Palliative Care

N/A
Recruiting
Led By Joshua K Pope
Research Sponsored by Prisma Health-Upstate
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Cognitively intact (has sufficient judgment, planning, organization, and self-control)
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 12 months
Awards & highlights

Study Summary

This trial is looking at how virtual reality and other outdoor experiences can help patients and their caregivers during end-of-life transitions. The researchers want to find strategies to support patients and caregivers during this difficult time.

Who is the study for?
This trial is for hospice patients experiencing end-of-life transitions and their caregivers. It aims to help with anxiety, pain, and psychological distress using a non-drug approach.Check my eligibility
What is being tested?
The study tests Tandem Virtual Reality experiences that simulate nature settings. Patients and caregivers use VR headsets together to see if it helps ease the emotional challenges of end-of-life care.See study design
What are the potential side effects?
Since this intervention uses virtual reality, side effects may include dizziness, nausea or motion sickness. Emotional responses to VR content can vary widely among individuals.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am mentally sharp and can make decisions for myself.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acceptance of Tandem VR
Fear of Death
Perceived benefits and value of Tandem VR
+2 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Tandem Virtual Reality ExperienceExperimental Treatment1 Intervention
Tandem VR Intervention After the surveys are completed, the researchers will share a personalized library of immersive, nature-based, 360-degree VR experiences for the participant-caregiver dyads to choose from based on their VR Intake Form. Once the dyad has determined their desired Tandem VR experience from the library, the researchers will assist the dyads in donning the VR head mounted display (HMD). The researchers will ensure the safety of both dyads while using the HMDs. The researchers will then initiate the Tandem VR experience. The duration of the Tandem VR experience will be 5-15 minutes.

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Who is running the clinical trial?

Prisma Health-UpstateLead Sponsor
83 Previous Clinical Trials
42,988 Total Patients Enrolled
Clemson UniversityOTHER
34 Previous Clinical Trials
5,943 Total Patients Enrolled
Joshua K PopePrincipal InvestigatorPrisma Health Hospice of the Foothills

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the current size of the patient cohort being observed in this clinical investigation?

"Indeed, the information available on clinicaltrials.gov confirms that this specific clinical trial is actively seeking eligible participants. The initial posting of the trial was made on January 1st, 2024 and it underwent its most recent update on December 15th, 2023. The study aims to recruit a total of 40 patients from one designated location."

Answered by AI

Are there any ongoing efforts to enroll participants in this research study?

"Indeed, as reported on clinicaltrials.gov, this ongoing clinical trial is currently seeking eligible patients. The trial was initially posted on January 1st, 2024 and has been recently updated on December 15th, 2023."

Answered by AI
~27 spots leftby Dec 2024