Feasibility, Usability, and Acceptability of Virtual Reality-Based Cognitive and Physical Rehabilitation in Individuals With Mild Cognitive Impairment
Part of paid clinical trials in Houston, Texas.
- Sponsor
- The University of Texas Health Science Center, Houston
- Study ID
- NCT07638748
- Status
- Not Yet Recruiting
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Conditions
- Mild Cognitive Impairment
- Subjective Cognitive Decline (SCD)
Eligibility Criteria
- Sex
- ALL
- Age
- 55 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- VR sessions — DEVICEParticipants will complete 3 supervised VR sessions using the Real System™ VR headset, per week for 6 weeks, for a total of 18 sessions. Each session will last approximately 60 minutes, with time allocated for setup and brief symptom checks
Study Details
The purpose of this study is to demonstrate feasibility, usability, and acceptability of VR-based cognitive and physical rehabilitation, evaluate adherence, tolerability, and fidelity to the VR intervention and explore preliminary effectiveness of VR-based rehabilitation on cognitive, physical, and functional outcomes
Key Dates
- Start date
- Jun 12, 2026
- Status verified
- Jun 2026
- Primary completion
- Oct 15, 2026
- Completion
- Nov 30, 2026
Study Design
- Enrollment
- 10 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DEVICE_FEASIBILITY
Arms
- Experimental: VR sessions
Primary Outcome Measure
Feasibility as assessed by the recruitment rate [ Time Frame: from baseline to end of intervention (6 weeks) ]
Central Contacts
- Seema S Aggarwal, PhD, APRN, AGNP-C(713) 500-9946
- Tela Todd(713) 500-7039
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Texas Health Science Center at Houston | Houston | Texas | 77030 |
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