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NCT03144921Completed

EPIC: An Intervention for Early-stage AD Dyads - Adapted for Virtual Delivery

EPIC: A Group-based Intervention for Early-stage AD Dyads in Diverse Communities

Source: ClinicalTrials.gov · Last updated 6 Aug 2024

Brief summary (registry, in English)

EPIC II (Early-Stage Partners in Care) is a research project designed to assist people with early-stage memory loss and their care partners by providing early-stage related education and skill-training sessions, held via Zoom, designed to reduce stress, enhance well-being, manage challenges, and plan for the future. Researchers will gather feedback from individuals about their experience to continue to improve programs for early-stage memory loss.

Status (registry)
Completed
Study type
Interventional
Enrollment
272 (actual)
First submitted
2 May 2017
Start date
12 Dec 2017
Primary completion date
30 Apr 2024
Lead sponsor
Arizona State University
NCT number
NCT03144921

What you commit to

  • Study type: Interventional
  • Participants enrolled: 272
  • From 12 Dec 2017 to the primary completion date, 30 Apr 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • DYAD INCLUSION CRITERIA:
  • All participants - Care Partners (CP) and Early-Stage People (EP) - will be at least 18 years of age and speak, read, and write English or Spanish.
  • Eligible dyad relationships include spouse, adult-child relationships (e.g., daughters), and other close friends and family members.
  • Care partners must self-identify as the person who currently has or who expects to have the most hands-on responsibility and ongoing involvement with the EP.
  • CPs must live with or have regular contact with the EP.
  • EPs and CPs must reside in a community setting.
    • EP INCLUSION CRITERIA:
  • Live at home rather than an institutional setting,
  • Have a confirmed diagnosis of OR symptoms consistent with early-stage dementia
  • Exhibit changes in memory as specified on the AD8 dementia screening tool.
  • Have a Mini-Mental State Exam (MMSE)i score within a protocol-specified range.
  • Have a CP who is defined by the EP as being the unpaid "family member" who has or will have primary responsibility for providing assistance to the EP
    • EP EXCLUSION CRITERIA:
  • Denying or not reporting any trouble with memory, based on self-report
  • Normal cognition, based on score derived from screening tool
  • If yes to BOTH:
    • severe mental illness or developmental disability before the age of 45
    • memory problems due to past head injury

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Nationwide Program Locations (Based at ASU Edson College of Nursing and Health Innovation)
Coordinator of this site? Confirm its status
PhoenixUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.