NCT06418971Recruiting
Testing & Refinement of CarePair: An Assessment and Referral Platform to Support Family Caregivers of Alzheimer's Disease and Related Dementias.
Source: ClinicalTrials.gov · Last updated 5 Mar 2026
Brief summary (registry, in English)
The purpose of this study is to develop and test CarePair, a mobile application-based needs assessment and service referral platform for family caregivers of persons with dementia designed to alleviate stress and promote psychosocial well being. The main aims of this study are: * To evaluate the feasibility and acceptability of the CarePair mobile application. * To explore the potential for CarePair to reduce feelings of depression and burden, and improve caregivers' feelings of self-efficacy. Caregiver participants will be asked to log in and use the CarePair application and complete study activities for a six-week duration. Researchers will compare the intervention group to an attention control comparator to see if application use is associated with improved psychosocial outcomes at follow-up.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 27 Feb 2024
- Start date
- 15 Sept 2025
- Primary completion date
- 31 Jul 2026
- Lead sponsor
- University of Southern California
- Diseases
- Alzheimer disease
- NCT number
- NCT06418971
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 15 Sept 2025 to the primary completion date, 31 Jul 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- Inclusion:
- Currently a primary caregiver of a community-dwelling PwD
- Provides at least 10 hours of care per week
- ≥18 years of age
- Fluent in English
- Both the caregiver and care-recipient reside in and/or can easily access one of the following cities/areas: New York City, New York (NY); Long Island, NY; Westchester County, NY; Seattle, Washington (WA); Los Angeles, California (CA)
- Provides at least 10 hours of care per week
- Has provided care for at least 6 months
- Able to use the internet and has internet access
- Owns and can operate a smartphone
- Able and willing to provide their informed consent to participate for the six-week study duration
- Does not self-report any cognitive impairments
- Exclusion:
- Not currently the primary caregiver of a community-dwelling person with dementia
- Care-recipient lives in residential care (e.g., assisted living, skilled nursing facility)
- ≤18 years of age
- Not fluent in English
- The caregiver and/or care-recipient resides outside of and/or cannot easily access any of the following cities: New York City (NY); Long Island (NY); Westchester County (NY); Seattle (WA); Los Angeles (CA)
- Provides less than 10 hours of care per week
- Has provided care for less than 6 months
- Unable to use the internet or does not have internet access
- Does not own and/or cannot operate a smartphone
- Unable or unwilling to provide informed consent to participate for the six-week study duration
- Self-reports having a cognitive impairment
Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Southern California Coordinator of this site? Confirm its status | Los Angeles | United States | Recruiting |
Related publications
This page is information, not medical advice. Discuss any trial with your doctor.