Testing & Refinement of CarePair: An Assessment and Referral Platform to Support Family Caregivers of Alzheimer's Disease and Related Dementias.
Recruiting · NCT06418971 · Interventional (participants receive a specific treatment) · Lead sponsor:
University of Southern California
View the official record on ClinicalTrials.gov →
Interventions studied
CarePair
What this trial is about
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.
Who can take part
Age range
18 Years and older
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Eligibility criteria (as published)
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
Where it is running
1 location listed across 1 US state.
Read the full protocol, contacts and eligibility on ClinicalTrials.gov →