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NCT06095661 · ClinicalTrials.gov registry record · NA
Virtual Reality as a Postoperative Pain Management Adjunct in Older Adults: An Acceptability and Feasibility Study
A NA study, sponsored by University of California, San Francisco.
- Completed
- Registry status
- NA
- Development phase
- 29
- Enrollment target
NCT06095661 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 29 participants.
The verdict
NCT06095661, a NA study, has completed, sponsored by University of California, San Francisco.
- COMPLETED
- Registry status
- NA
- Development phase
- 29 participants
- Enrollment target
Study Summary
This single-arm mixed methods study aims to determine potential differences in self-reported postoperative pain intensity levels, anxiety, and state of relaxation through immediate pre-post intervention evaluation among those aged 65 or older who receive immersive virtual reality during their hospitalization, up to three days following major elective surgery. In addition, the investigators will evaluate the feasibility and acceptability of virtual reality for use in this older adult population. This study will not evaluate the efficacy of VR. The main questions this study seeks to answer are: 1. What is the feasibility and acceptability of using immersive virtual reality to impact clinical outcomes such as pain, anxiety, and relaxation in older adults who have undergone major elective surgery? 2. What is the older adult's user experience with virtual reality during hospitalization up to the three days following major elective surgery?
Interventions
- OTHER REAL System i-Series VR head-mounted display (HMD) from Penumbra, Inc.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 29 participants |
| Start Date | 2023-10-26 |
| Est. Completion | 2024-06-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06095661
The ClinicalTrials.gov registry entry for NCT06095661 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 29 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which REAL System i-Series VR head-mounted display (HMD) from Penumbra, Inc. is the first listed.
NCT06095661 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06095661 about?
NCT06095661 is a clinical study titled "Virtual Reality as a Postoperative Pain Management Adjunct in Older Adults: An Acceptability and Feasibility Study". This single-arm mixed methods study aims to determine potential differences in self-reported postoperative pain intensity levels, anxiety, and state of relaxation through immediate pre-post intervention evaluation among those aged 65 or older who receive immersive virtual reality during their hospit...
What is the current status of trial NCT06095661?
This trial is currently completed. It is a NA study. The enrollment target is 29 participants. The study started on 2023-10-26. Estimated completion is 2024-06-01.
What interventions are being tested in trial NCT06095661?
The interventions under investigation include: REAL System i-Series VR head-mounted display (HMD) from Penumbra, Inc. (OTHER).
Who is sponsoring clinical trial NCT06095661?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
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