Addressing Emotional Distress in Dyads of Persons With a Young Onset Dementia (YOD) and Their Care-partners
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Massachusetts General Hospital
- Study ID
- NCT07018726
- Status
- Recruiting
Conditions
- Young Onset Dementia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Resilient Together-YOD — BEHAVIORALThis is a 6 session dyadic (patient and spousal care-partner) intervention that teaches resiliency and interpersonal communication skills early after YOD diagnoses. It aims to decrease heightened symptoms of depression and anxiety among dyads to help them engage in important decisions around long term care-planning and optimize adjustment. The goal is to equip dyads with the necessary skills to cope and engage in meaningful, challenging conversations around care-planning, symptom deterioration, work/family planning to improve well-being in both members of the dyad.
- Health Enhancement Program-YOD — BEHAVIORALThis is a 6 session program that will deliver educational information to dyads and will mimic the dose and duration of Resilient Together. The program will not teach any individual and dyadic interpersonal skills, but will contain education on psychological distress and healthy behaviors. Sessions will also be delivered virtually.
Study Details
The purpose of the present investigation is to test the efficacy of a virtual, brief (6 sessions) dyadic (patient and care-partner together) intervention to prevent chronic emotional distress in dyads where one person is diagnosed with Young Onset Dementia (YOD). Through this study, we seek to address the unmet need of preventing chronic emotional distress in YOD dyads through a feasible, acceptable and credible program, and ideally enhance resiliency and improve wellbeing and quality of life in both members of the dyad.
Key Dates
- Start date
- Jan 28, 2026
- Status verified
- Apr 2026
- Primary completion
- Jul 1, 2030
- Completion
- Jan 1, 2031
Study Design
- Enrollment
- 388 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Experimental: Experimental Patient-Caregiver DyadsThere will be 6 sessions delivered via live video using Zoom. Content will be primarily skills.
- Active Comparator: Control Patient-Caregiver DyadsThere will be 6 sessions delivered via live video using Zoom. Content will be primarily educational.
Primary Outcome Measure
Change in Emotional Distress [ Time Frame: 0 weeks, 6 weeks, 12 weeks ]
Central Contacts
- Ana-Maria Vranceanu, PhD617-724-4977
- Maggie L Syme, PhD, MPH
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Massachusetts General Hospital (MGH) | Boston | Massachusetts | 02114 | Ana-Maria Vranceanu, PhD (PRINCIPAL_INVESTIGATOR) |
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