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Dementia / Compass for Care (Well-being intervention) / Mental Health · Interventional Study
ClinicalTrials.gov · August 11, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a Phase II interventional study of a mobile behavioral intervention (Compass for Care) designed to reduce caregiver burden among individuals caring for people with Alzheimer's disease or related dementia. Recruitment is complete but results have not yet been posted in this registry record, precluding assessment of efficacy.
Interventional, Randomized, Parallel, Single masking, Treatment purpose. Dementia, Mental Health; age from 18 Years; accepts healthy volunteers. Intervention: Compass for Care (Well-being intervention). Compared with: Compass for Care (Safety intervention) — Active Comparator. n = 278. 1 site: United States.
This is a Phase II interventional study of a mobile behavioral intervention (Compass for Care) designed to reduce caregiver burden among individuals caring for people with Alzheimer's disease or related dementia. Recruitment is complete but results have not yet been posted in this registry record, precluding assessment of efficacy.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
Results are not yet available in this registry record. Once published, findings will inform whether this digital self-care behavior intervention reduces caregiver burden, a critical outcome given that ADRD caregivers experience depression at rates 6–7 times higher than the general population.
Phase II interventional study with recruitment completed but no results posted in registry; design and outcomes are planned rather than observed.
As stated by the source record.
Quoted from the source exactly as published.
Results are not yet available in this registry record. Once published, findings will inform whether this digital self-care behavior intervention reduces caregiver burden, a critical outcome given that ADRD caregivers experience depression at rates 6–7 times higher than the general population.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT06249139). This is a study registration, not published results. Lead sponsor: Pro-Change Behavior Systems. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 278 participants (ACTUAL). Conditions: Dementia, Mental Health. Interventions: BEHAVIORAL: Compass for Care (Well-being intervention); BEHAVIORAL: Compass for Care (Safety intervention). Primary outcome measures: Zarit Burden Interview (ZBI) , Baseline, 3, 6, and 9 months' follow-up. Brief summary: 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.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.