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Study identifier: NCT07430371 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Virtual Reality for Caregiver Assembly, Relief, Empowerment, and Support (VR-CARES)

Condition: Direct Care Workers · Dementia Caregiver · In-Home Care  ·  Sponsor: Rendever, Inc.

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

The VR-CARES project is an innovative, collaborative effort that invites dementia care professionals into the design process of a virtual reality platform seeking to mitigate their work-related burden and social isolation by cultivating a virtual community of support. The co-created, caregiver-specific VR platform will serve as a safe, communal space where caregivers can remotely connect with their peers, share fun experiences together, access support, learn self-care and build resilience within a supportive virtual network to enhance their social and mental health and job satisfaction. Central to VR-CARES in the principle of user-led innovation, ensuring that the technology not only serves but is informed and successfully adopted by the very individuals it intends to benefit, an important standard for empathetic and inclusive technology in healthcare.

This description comes directly from the study's public registry record.

Talk to the study team

Jennifer Stamps, PhD, PhD  ·  904-476-1350  ·  jennifer@rendever.com

Julia Bandini, PhD, PhD  ·  617-338-2059  ·  jbandini@rand.org

Always discuss trial participation with your own doctor first.

Locations (8)

Comfort Keepers Home CareSan Diego, California, United StatesRecruiting
Rendever, Inc.Boston, Massachusetts, United StatesRecruiting
Right at HomeSalem, Massachusetts, United StatesRecruiting
Right at HomeBrighton, Michigan, United StatesRecruiting
Right at HomeEast Lansing, Michigan, United StatesRecruiting
Right at HomeNovi, Michigan, United StatesRecruiting
Right at HomeOwosso, Michigan, United StatesRecruiting
Halcyon HomeAustin, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07430371