A digital lifeline for dementia caregivers: can Self-Care modules ease the burden?
NCT ID NCT06249139
First seen Aug 11, 2026 · Last updated Aug 12, 2026 · Updated 1 time
Summary
This study tests a mobile program called Compass for Care, designed to help people caring for a loved one with Alzheimer's or related dementias. The program delivers 12 weekly modules and tailored messages focusing on five self-care behaviors, such as taking time to recharge and seeking emotional support. Researchers will measure whether the program reduces caregiver burden and depression compared to a safety-focused version. Participants are unpaid caregivers in the U.S. who provide at least 8 hours of care per week.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Compass for Care, a digital behavioral program with 12 weekly modules and tailored messages to support self-care behaviors
- What this could lead to
- If effective, this digital program could offer a scalable way to reduce stress and depression among the millions of unpaid dementia caregivers, improving their well-being.
- What could go wrong
- The trial is a mid-stage study, and results may not generalize to all caregivers. Success depends on engagement, and the program may not reduce burden for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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278 people
The number who actually took part.
- Started
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Nov 2023
- Finished
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Aug 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Able to read and speak English 2. Aged 18+ 3. Residing in the U.S. 4. Regularly use the internet 5. Agree to receive daily messages by email or text during the 3-month intervention period 6. 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 7. Have been providing care for at least 3 months; 8. 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) 9. 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 Exclusion Criteria: 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)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Pro-Change Behavior Systems
Narragansett, Rhode Island, 02882, United States
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