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
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

  • Virtual Reality (VR) sessions — DEVICE
    Participants will complete 3 supervised virtual reality (VR) sessions per week for 6 weeks for a total of 18 sessions using either the Real System VR headset or the Oculus Quest 2 VR headset. 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 virtual reality (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

First listed
Jun 10, 2026
Start date
Jun 18, 2026
Status verified
Aug 2026
Primary completion
Nov 13, 2026
Completion
Nov 13, 2026

Study Design

Enrollment
10 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY

Arms

  • Experimental: Virtual Reality (VR) sessions

Primary Outcome Measure

Feasibility as assessed by the recruitment rate [ Time Frame: from baseline to end of intervention (6 weeks) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The University of Texas Health Science Center at HoustonHoustonTexas77030
Seema Aggarwal, PhD, APRN, AGNP-C
[email protected]
(713) 500-9946
Tela Todd
[email protected]
(713) 500-7039

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The University of Texas Health Science Center at Houston· Houston, TX

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