In-Home Technology for Caregivers of People With Dementia and Mild Cognitive Impairment
NCT04206670 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 216
Last updated 2022-05-10
Summary
This study aims to develop and evaluate new in-home supportive technology that is designed to alleviate anxiety, burden, and loneliness in spousal and familial caregivers of individuals with Alzheimer's disease, other dementias, or mild cognitive impairment.
Conditions
- Dementia
- Mild Cognitive Impairment
- Alzheimer Disease
Interventions
- DEVICE
-
In-Home Technology System and Questionnaires
Participants self-install the in-home technology system in their homes after enrollment in the study (i.e., consent procedures and initial questionnaire). Intelligent bots monitor the in-home sensors, learn typical patterns, and provide caregivers with text messages via cell phone and alerts via the tablet when worrisome behaviors occur. Social contact is encouraged using caregiver resources and a trusted circle of friends and family who are encouraged to stay in contact with the caregiver and person with dementia or mild cognitive impairment.
- DEVICE
-
Waiting Control In-Home Technology System and Questionnaires
Participants self-install the in-home technology system in their homes six months after their enrollment in the study (i.e., consent procedures and initial questionnaire). Intelligent bots monitor the in-home sensors, learn typical patterns, and provide caregivers with text messages via cell phone and alerts via the tablet when worrisome behaviors occur. Social contact is encouraged using caregiver resources and a trusted circle of friends and family who are encouraged to stay in contact with the caregiver and person with dementia or mild cognitive impairment.
Sponsors & Collaborators
-
People Power Company
collaborator INDUSTRY -
National Institute on Aging (NIA)
collaborator NIH -
University of California, San Francisco
collaborator OTHER -
University of California, Berkeley
lead OTHER
Principal Investigators
-
Robert W Levenson, Ph.D. · University of California, Berkeley
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-03-10
- Primary Completion
- 2021-12-08
- Completion
- 2021-12-08
Countries
- United States
Study Locations
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