Clinical trial Recruiting at 1 site Interventional Ages 19 and up

Transitional care intervention for Alzheimer's patients and their caregivers

Official title: Transitional Care for Skilled Nursing Facility Patients With Alzheimer's Disease and Related Dementias and Their Caregivers: a Cluster Randomized Trial

Run by University of North Carolina, Chapel Hill · NCT06840587 · Data updated 2026-11-12

This study tests a new program to help Alzheimer's patients and their caregivers adjust better when moving from nursing homes to home or other care settings.

More Dementia trials

Quick facts

Study typeInterventional
Ages19 Years and up
SexAll
Enrollment360 (estimated)
SponsorUniversity of North Carolina, Chapel Hill
Academic / other
Locations1 site (Chapel Hill, North Carolina)
StatusRecruiting
StartedApril 4, 2025
Main results expectedJune 30, 2027
Study endsJune 30, 2027
Registry record updatedMarch 30, 2026
Trial IDNCT06840587 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include English-speaking patients diagnosed with dementia who are transitioning to home, assisted living, or long-term care, along with their willing caregivers.

Probably not a fit

Patients who are planned for hospital readmission within 30 days post-enrollment 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 study tests the efficacy of the Connect-Home ADRD intervention, which aims to support patients with Alzheimer's disease and related dementias (ADRD) and their caregivers during transitions from Skilled Nursing Facilities (SNFs) to home or other care settings. It employs a cluster randomized trial design involving 12 SNFs in North Carolina, where half will receive the intervention and half will serve as a control group. The primary goals are to reduce caregiver strain and improve patient neuropsychiatric symptoms through structured support from Dementia Caregiving Specialists.

Why it matters

Potential benefit: If successful, this intervention could significantly alleviate caregiver burden and improve the quality of life for patients with Alzheimer's and related dementias.

How similar studies have gone: Other studies have shown promise in transitional care interventions for dementia patients, suggesting potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Patients:

* Ability to speak English
* Goal of discharge to home, assisted living, or long-term care
* Diagnosis of dementia
* Having a caregiver willing to participate

Caregivers:

* Ability to speak English
* Legally authorized representative (LAR) who also provides support for the person with ADRD

Inclusion criteria for SNFs:

* Location within 120 miles of UNC-Chapel Hill
* Admission of at least 75 SNF patients per year

Exclusion Criteria:

Patients:

* Planned hospital readmission for procedures or treatments within 30 days post enrollment.

Caregivers:

* LAR is a court-appointed guardian.

Where it's running

  • University of North Carolina at Chapel Hill
    Chapel Hill, North Carolina, United States
    Recruiting

Study contacts

  • Principal investigator: Mark Toles, PhD, RN — University of North Carolina, Chapel Hill
  • Study coordinator: Molly Lynch, MS
  • Email: molly_lynch@unc.edu
  • Phone: 9198438874

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.