- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07183839
- Original Trial
The Effect of Immersive VR Distraction on Memory: Study 2
September 19, 2025 updated by: Hunter Hoffman, University of Washington
Immersive Virtual Reality Induces Procedural Analgesia, Anxiolysis and Anterograde Amnesia:A Randomized Controlled Study 2
This study measures how many words people can recall.
Some words are studied/heard/learned while in immersive Virtual Reality, and some are studied/heard/learned while in a plausible control distraction.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In this Study (n=20), participants recalled word lists during a plausible semi-immersive control condition (passive Apple Vision Pro see-through mode) versus during interactive immersive VR.
Participants also later received brief heat pain stimuli during No VR versus immersive VR and provided pain and anxiety and distraction ratings on 0-10 graphic rating scales.
Study Type
Interventional
Enrollment (Actual)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Washington
-
Seattle, Washington, United States, 98195
- University of Washington
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Currently enrolled in a course at the University of Washington Psychology Dept., participating in the UW Psychology subject pool
- Able to read, write and comprehend English
- Able to complete study measures
- Willing to follow our UW approved instructions
- 18 years of age or older
Exclusion Criteria:
- People who have already previously participated in this same study (e.g., last quarter) are not eligible to participate again.
- Not enrolled in a course at the University of Washington Psychology Dept., not participating in the UW Psychology subject pool
- Not be able to read, write and comprehend English
- Younger than 18 years of age.
- Not capable of completing measures
- Not capable of indicating pain intensity,
- Not capable of filling out study measures,
- Extreme susceptibility to motion sickness,
- Seizure history,
- Unusual sensitivity or lack of sensitivity to pain,
- Sensitive skin,
- Sensitive feet
- Migraines
- Diabetes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High Tech virtual reality
Participants used their cyberhands to interact with virtual objects while in immersive virtual reality, while they listen to and memorize a list of 15 study words rea to them from the real world.
|
While wearing an immersive VR helmet, participants grabbed virtual objects andd put them into a bowl of virtual water, while memorizing a list of words from the real world.
|
|
Sham Comparator: Low Tech VR
Participants wore an Apple Vision Pro VR goggles that allowed them to see the real world in their VR goggles, via video streaming from cameras mounted on the VR helmet, while memorizing a list of words they heard from the real world.
|
Participant passively viewed the laboratory room they saw while wearing Apple Vision Pro goggles, while memorizing a list of words read to them from the real world.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Word Recall accuracy
Time Frame: begin 15 seconds after the last word
|
Number of study words recalled during an immediate recall task
|
begin 15 seconds after the last word
|
|
Subjective ratings of Distraction
Time Frame: Measured immediately after the free recall of each word list.
|
Participants rated how distracted they were in each treatment condition
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Measured immediately after the free recall of each word list.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
During Phase 2, VR pain reduction was measured
Time Frame: subjective pain ratings measured immediately after each brief thermal stimulus
|
graphic ratings of worst pain intensity and other GRS pain ratings during brief thermal stimulation
|
subjective pain ratings measured immediately after each brief thermal stimulus
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: HUNTER HOFFMAN, PhD, University of Washington
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 31, 2024
Primary Completion (Actual)
February 11, 2025
Study Completion (Actual)
February 11, 2025
Study Registration Dates
First Submitted
September 10, 2025
First Submitted That Met QC Criteria
September 14, 2025
First Posted (Estimated)
September 19, 2025
Study Record Updates
Last Update Posted (Estimated)
September 24, 2025
Last Update Submitted That Met QC Criteria
September 19, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- VRAnalgesia2025b
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
De-identified summarized aggregated data will be available upon reasonable request.
IPD Sharing Time Frame
De-identified summarized aggregated data will be available upon publication in a peer reviewed journal until 2030
IPD Sharing Access Criteria
summarized aggregate data will be made available upon reasonable request by e-mailing the primary contact.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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