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NCT06249139Completed

Compass for Care: A Theory-driven Mobile Solution to Promote Well-being Among Caregivers of Individuals With ADRD

Caring4Caregivers: A Theory-driven Mobile Solution to Promote Self-care and Well-being Among Caregivers of Individuals With Alzheimer's and Related Dementias

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

In the US, the over 11 million Americans currently providing unpaid care to a family member, relative, or friend with Alzheimer's disease or a related dementia (ADRD) are over 6 times more likely than the general population to suffer from depression (33.9% vs. 5%), and nearly 60% rate their emotional distress as high or very high. The purpose of this Phase II research is to continue the successful work of the pilot development and testing by conducting a rigorous scientific study of the effects of Compass for Care, a digital program that customizes behavior change guidance for using five self-care behaviors critical to ADRD caregiver well-being: 1) taking time to recharge; 2) finding information about your loved one's diagnosis and needs; 3) discovering your strengths and limits; 4) exploring outside help; and 5) seeking emotional support.

Status (registry)
Completed
Study type
Interventional
Enrollment
278 (actual)
First submitted
31 Jan 2024
Start date
13 Nov 2023
Primary completion date
1 Aug 2025
Lead sponsor
Pro-Change Behavior Systems
NCT number
NCT06249139

What you commit to

  • Study type: Interventional
  • Participants enrolled: 278
  • From 13 Nov 2023 to the primary completion date, 1 Aug 2025
  • 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.

Other

  • 1\. Indicating suicidal ideation based upon the Patient Health Questionnaire (PHQ)-9 suicidality ideation item (i.e., Thoughts that you would be better off dead, or of hurting yourself)

Who the study is looking for

  • Able to read and speak English
  • Aged 18+
  • Residing in the U.S.
  • Regularly use the internet
  • Agree to receive daily messages by email or text during the 3-month intervention period
  • Currently providing at least 8 hours of unpaid care to a family member or friend diagnosed with Alzheimer's disease, Lewy body dementia, frontotemporal dementia, vascular dementia, dementia type not specified, or mixed dementia
  • Have been providing care for at least 3 months;
  • Score of 3 or higher on the Zarit burden item (Overall, how burdened do you feel in caring for your relative) OR a score of 2 on this item and a score of 2+ on the Patient Health Questionnaire (PHQ)-2 assessment (i.e., Little interest or pleasure in doing things; Feeling down, depressed, or hopeless)
  • Expecting to provide care to their family member or friend for at least three more months, or don't know how much longer they will be providing care

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Pro-Change Behavior Systems
Coordinator of this site? Confirm its status
NarragansettUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.