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Life sciences · Interventional Study
ClinicalTrials.gov · October 2, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07631247). This is a study registration, not published results. Lead sponsor: Dartmouth-Hitchcock Medical Center. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 15 participants (ESTIMATED). Conditions: Depression - Major Depressive Disorder. Interventions: OTHER: depression app for care partners of persons with dementia. Primary outcome measures: Usability of Intervention , Assessed after initial use of iPath app at T1 (2 weeks); Acceptability of Intervention , Assessed at end of study, T1 (2 weeks); Feasibility of Intervention , Assessed at end of study, T1 (2 weeks); Appropriateness of Intervention , Assessed at end of study, T1 (2 weeks); Treatment access , Assessed at end of study, T1 (2 weeks); Mental health literacy , Change between T0 and T1 (2 weeks). Brief summary: Depression is a significant problem in care partners of people living with dementia; despite the expansion of options for accessing evidence-based treatments, most care partners of people living with dementia are not screened for depression and do not receive treatment. The objective of this project is to identify a screening method for depression that is feasible and acceptable to care partners and to adapt an innovative pathway to online evidence-based treatment for depression (iPath\*D) as a means of increasing mental health literacy, screening rates and treatment access for care partners of people living with dementia. The results are expected to have a major positive impact by providing proof-of-principle for the use of an online pathway to evidence based treatment with the potential for reaching an unprecedented number of care partners who have unmet mental health needs.