Thrive at Home: A Virtual Reality Social Intervention for Older Adults
- NCT ID
- NCT07835568
- Registry status
- Not yet recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- University of California, Santa Barbara
- Conditions
- Alzheimer Dementia (AD), Caregiver Burden, Caregiver Wellbeing, Dementia, Loneliness, Mental Health (Depression), Mental Health and General Well-being, Mild Cognitive Impairment(MCI), Well Being
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Official title: Improving Mental Health and Social Connectivity for Older Adults Through Virtual Reality-Based Social Interventions
Enrollment: 250 participants (Estimated).
What is being studied
- Behavioral: Abbreviated Virtual Reality Social Intervention
- Behavioral: Full Virtual Reality Social Intervention
Who may be eligible
- Ages
- 65 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- Yes
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
PRIMARY PARTICIPANTS (OLDER ADULTS):
* Aged 65 years or older.
* Living in a private residence and receiving home care services from a participating provider, with services expected to continue for the duration of the study (approximately 4 months).
* Montreal Cognitive Assessment (MoCA) score of 12 or above.
* Fluent in English, sufficient to participate in group virtual reality (VR) sessions and complete verbal surveys.
* Adequate vision and hearing to complete surveys and engage with VR experiences (mild impairments acceptable if corrected).
* Has a family caregiver or home care professional available to support them at every VR session if the MoCA score is below 18 or the participant cannot physically manipulate the headset independently.
FAMILY CAREGIVERS (OPTIONAL SUBSTUDY):
* Aged 18 years or older.
* Identifies as the primary family caregiver for an enrolled primary participant (living with or visiting the primary participant at least twice per week).
* Fluent in English and able to complete online surveys on a personal digital device (e.g., smartphone, laptop, tablet, or computer).
Exclusion Criteria:
PRIMARY PARTICIPANTS (OLDER ADULTS):
* History of severe motion sickness or vertigo.
* History of seizures or epilepsy.
* Frequent and distressing hallucinations.
* Aphasia or other communication barriers preventing verbal participation.
* Severe disorientation or delirium.
* Frequent and severe outbursts or emotional dyscontrol, or frequent and severe aggressive tendencies. (Typical sundowning is not exclusionary.)
* Total vision loss not overcome by VR, or uncorrected hearing impairment that makes group conversation impracticable.
* Residence in a senior living community or other congregate housing.
* Presence of a harmful, aggressive, or abusive relationship with a family caregiver living in the home.
FAMILY CAREGIVERS (OPTIONAL SUBSTUDY):
* Presence of an aggressive or abusive relationship with the enrolled primary participant.
Study locations
No study locations are listed in the registry data.
Study details
- Start date
- October 1, 2026
- Primary completion date
- May 1, 2028
- Completion date
- May 1, 2028
- First posted
- September 23, 2026
- Collaborators
- National Institute on Aging (NIA), National Institutes of Health (NIH), Rendever, Inc.
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07835568
- Registry last updated
- September 25, 2026
- QualifiedStudies registry data refreshed
- September 28, 2026
- QualifiedStudies record fetched
- September 28, 2026
View NCT07835568 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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