A program to support couples dealing with dementia
Official title: Resilient Together for Dementia: A Live Video Resiliency Dyadic Intervention for Persons With Dementia and Their Care-partners Early After Diagnosis
Run by Icahn School of Medicine at Mount Sinai · NCT06619327 · Data updated 2026-11-12
This study is testing a new program called Resilient Together for Dementia to see if it can help couples cope better with the emotional challenges of dementia.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 24 (estimated) |
| Sponsor | Icahn School of Medicine at Mount Sinai Academic / other |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | February 19, 2025 |
| Main results expected | July 1, 2027 |
| Study ends | July 1, 2028 |
| Registry record updated | June 4, 2026 |
| Trial ID | NCT06619327 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include English-speaking couples living together, where one partner has a recent diagnosis of early-stage dementia and experiences significant emotional distress.
✕Probably not a fit
Patients who are deemed inappropriate by the neurology team or have co-occurring terminal illnesses may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This intervention focuses on couples where one partner has been diagnosed with dementia, aiming to reduce emotional distress and improve quality of life for both partners. The Resilient Together for Dementia (RT-D) program will be delivered via live video and is designed to prevent chronic emotional distress in at-risk dyads. A pilot randomized control trial will assess the feasibility and preliminary efficacy of RT-D compared to a minimally enhanced educational control. The study will involve 50 dyads and will evaluate various outcomes to inform future research phases.
Why it matters
Potential benefit: If successful, this program could significantly improve the emotional well-being and quality of life for couples affected by dementia.
How similar studies have gone: Other studies have shown promise in using dyadic interventions for emotional distress in dementia care, suggesting that this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Recent (\~3 month) chart documented ADRD diagnosis, * ADRD symptom onset after age 65 * Cognitive assessment scores and symptoms consistent with early stage dementia, as determined by the Clinical Dementia Rating Scale scores of .5 or 1.0 * Cognitive awareness of their problems (as determined by the treating neurologist), and ability to understand study and research protocol, as determined by a standardized teach-back method assessment Additional inclusion criteria for dyads are: * English speaking adults (18 years or older) * Dyad lives together * At least one partner endorses clinically significant emotional distress during screening (\>7 on Hospital Anxiety and Depression scale subscales or \<5 on the Geriatric Depression Scale) Exclusion Criteria: * Patient is deemed inappropriate by the neurology team * Either partner has a co-occurring terminal illness * Patient was diagnosed with forms of dementia with clinical profiles that would preclude participation (e.g., Frontotemporal Dementia- behavioral variant), as determined by treatment team.
Where it's running
-
Brain Injury Research Center at Mount Sinai
New York, New York, United States Recruiting
Study contacts
- Principal investigator: Sarah Bannon, PhD — Icahn School of Medicine at Mount Sinai
- Study coordinator: Sarah M. Bannon, PhD
- Email: sarah.bannon@mountsinai.org
- Phone: 212-241-0787
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.