- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06252025
Immersive VR Reminiscence System for Facilitating Memory Retrieval Among Nursing Home Older Adults
April 25, 2026 updated by: Zhu Dian
The Effect of an Immersive VR Reminiscence System for Facilitating Memory Retrieval Among Nursing Home Older Adults
A VR game "Memo-gration" was designed to assist elderly people in reminiscence therapy.
The ultimate scene design was crafted in a vintage Chinese aesthetic reminiscent of the previous century.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study tailored a variety of instructional material within each virtual scenario, taking into account various memory triggers.
Guidance is activated when the user is identified as making physical contact with an object or discussing a specific keyword.
This encompasses textual assistance provided within the virtual environment, the display of multimedia information, and the provision of organized voice guidance.
Following the system's instructions, users engaged in discussion with the caregiver, and had the freedom to terminate the conversation at their discretion and explore other topics by interacting with different items.
Study Type
Interventional
Enrollment (Actual)
36
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
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, China, 200140
- Dian Zhu
-
-
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:
- (i) absence of significant cognitive impairment, visual impairment, hearing impairment, and communication ability.
- (ii) Obtained the pre-test and watched the film while wearing a VR headgear without experiencing any notable discomfort.
Exclusion Criteria:
- (i) Older adults with cognitive impairments that prevent normal communication
- (ii) Visually impaired
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: VR reminiscence therapy system "Memo-gration"
This study tailored a variety of instructional material within each virtual scenario, taking into account various memory triggers.
Guidance is activated when the user is identified as making physical contact with an object or discussing a specific keyword.
This encompasses textual assistance provided within the virtual environment, the display of multimedia information, and the provision of organized voice guidance.
Following the system's instructions, users engaged in discussion with the caregiver, and had the freedom to terminate the conversation at their discretion and explore other topics by interacting with different items.
|
This study tailored a variety of instructional material within each virtual scenario, taking into account various memory triggers.
Guidance is activated when the user is identified as making physical contact with an object or discussing a specific keyword.
This encompasses textual assistance provided within the virtual environment, the display of multimedia information, and the provision of organized voice guidance.
Following the system's instructions, users engaged in discussion with the caregiver, and had the freedom to terminate the conversation at their discretion and explore other topics by interacting with different items.
|
|
Active Comparator: Picture reminiscence therapy
The picture reminiscence therapy group utilized a series of color images depicting screenshots of the Memo-gration, ensuring that the screenshots remained as consistent as feasible with the presented memory cues.
|
Picture reminiscence therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Profile of Mood States (POMS)
Time Frame: baseline and 1 day (study completion)
|
POMS is utilized to evaluate alterations in affective state and cognitive state induced by short-term psychotherapy, emotional stimuli, etc.Participants assessed their present mental state using a 5-point Likert scale, comprising 40 questions that encompassed 7 subscales measuring tension, despair, weariness, and self-esteem, etc.
A comprehensive mood disturbance score (TMD) was ultimately synthesized.
|
baseline and 1 day (study completion)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Questionnaire on VR Experience
Time Frame: 1 day (study completion)
|
The UMUX-Lite and Slater-Usoh-Steed Proximity Questionnaires are combined to investigate the user experience of older persons with Memo-gration.
Both assessments employ a 7-point Likert scale format.
|
1 day (study completion)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Dian Zhu, Dr, Shanghai Jiao Tong University School of Medicine
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)
July 1, 2023
Primary Completion (Actual)
July 1, 2024
Study Completion (Actual)
August 1, 2024
Study Registration Dates
First Submitted
January 24, 2024
First Submitted That Met QC Criteria
February 8, 2024
First Posted (Actual)
February 9, 2024
Study Record Updates
Last Update Posted (Actual)
April 28, 2026
Last Update Submitted That Met QC Criteria
April 25, 2026
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Sjtu0003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.
Clinical Trials on Emotional Regulation
-
University Rovira i VirgiliActive, not recruitingEmotional RegulationSpain
-
University of SurreyFrieslandCampinaCompletedEmotional RegulationUnited Kingdom
-
Babes-Bolyai UniversityThe Executive Agency for Higher Education, Research, Development and Innovation...CompletedEmotional RegulationRomania
-
Neuromotion LabsCompleted
-
Neuromotion LabsNot yet recruitingEmotional Regulation
-
King's College LondonGendered IntelligenceCompletedEmotional RegulationUnited Kingdom
-
Selcuk Universityaile ve sosyal hizmetler bakanlığıActive, not recruitingEmotion Regulation | Emotional Intelligence | Empathy SkillsTurkey (Türkiye)
-
Oklahoma State University Center for Health SciencesActive, not recruitingEmotional RegulationUnited States
-
Neuromotion LabsCompleted
Clinical Trials on Memo-gration
-
Asan Medical CenterRecruitingEmbolic Stroke of Undetermined SourceSouth Korea
-
HUINNO Co., LtdNot yet recruitingAtrial Fibrillation (AF)Korea, Republic of
-
OrygenNational Health and Medical Research Council, Australia; University of Melbourne and other collaboratorsCompleted
-
Innovation AlzheimerCentre Hospitalier Universitaire de Nice; Alzheimer's Association; Université...CompletedNeurocognitive DisordersFrance
-
Yonsei UniversityNot yet recruitingAtrial Fibrillation | Bradycardia | Ventricular Tachycardia | Supraventricular Tachycardia | Hospitalization | Arrhythmias | Patient Monitoring | TelemetrySouth Korea
-
Yonsei UniversityCompletedAtrial Fibrillation/Flutter in Patients With High Risk of StrokeSouth Korea
-
Sorin Group USA, Inc.CompletedMitral Valve RegurgitationUnited States, Canada
-
University Hospital, GhentLivaNovaCompleted
-
McGill University Health Centre/Research Institute...CompletedMild Cognitive ImpairmentCanada
-
University of California, San FranciscoTerminated