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NCT03896711Completed

MEMORI Corps: Activity-based Companion Care for Dementia

MEMORI Corps: A Novel Activity-based Companion Care Program to Benefit Community-living Persons With Dementia, Their Families, and Senior Volunteers

Source: ClinicalTrials.gov · Last updated 28 Jan 2026

Brief summary (registry, in English)

This project adapts a novel activity-based companion care model, the Making Engagement Meaningful through Organized Routine Interaction (MEMORI) Corps intervention, for a virtual delivery format, and then implements the intervention in a pilot, two-arm, randomized controlled trial to evaluate intervention acceptability, feasibility, and preliminary efficacy versus an augmented waitlist control. MEMORI Corps is a companion care model that provides regular companionship and personalized activities to community-living persons with dementia (PWD) delivered by trained volunteer Companion Guides 55 years of age or older. Program goals are to reduce social isolation and improve health and well-being for PWD, reduce burden and provide support to family CGs, as well as provide health benefits and opportunities for meaningful engagement for older volunteer Companion Guides.

Status (registry)
Completed
Study type
Interventional
Enrollment
175 (actual)
First submitted
28 Mar 2019
Start date
1 Mar 2022
Primary completion date
12 Aug 2024
Lead sponsor
Johns Hopkins University
NCT number
NCT03896711

What you commit to

  • Study type: Interventional
  • Participants enrolled: 175
  • From 1 Mar 2022 to the primary completion date, 12 Aug 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.

Other illness

  • At end-stage disease (e.g. bed-bound and non-communicative, or hospice),
  • Currently enrolled in a dementia related clinical trial, or
  • Report having an existing cognitive disorder diagnosis by a health provider (e.g., Mild Cognitive Impairment, Alzheimer's disease or other type of dementia).

Other

  • PWD are excluded if:
  • Deemed to be in a crisis/unsafe situation at baseline,
  • Planned transition from home in less than 6 months,
  • Deemed to have severe behavioral symptoms so severe that participation in this study is unsafe (e.g., are placing self or others at harm).
    • CGs are excluded if:
  • Do not plan to be co-residing with the PWD in the next 6 months, or
  • Currently involved in a behavioral/educational clinical trial.
    • Volunteers are excluded:
  • Planning on moving from the area in the next 12 months,
  • Unable to provide informed consent, and

Who the study is looking for

  • Persons with dementia and informal caregiver (PWD/CG) must both meet eligibility criteria. These criteria are designed to reduce PWD/CG attrition and ensure safety of PWD, CG, and volunteers.
  • PWD are eligible if:
  • English speaking;
  • Have an established physician clinical diagnosis of dementia (any stage) and confirmed with Informant Questionnaire on Cognitive Decline in the. Elderly (IQCODE) cut off \>=52 ,
  • Are able to participate in at least 4 basic Activities of Daily Living (out of 11),
  • Have not received formal (i.e., in-home companion care, or adult day center) activity-focused care services in the past 4 weeks,
  • Living at home in all counties in Maryland and Baltimore City,
  • Have a co-residing informal caregiver willing to participate as study partner, and 30 years old or older.
    • CG are eligible if:
  • English speaking,
  • 21 years of age or older (male or female),
  • Deemed to be a reliable informal caregiver (not paid for caregiving of PWD) who knows the PWD well,
  • Co-residing with the PWD, and
  • Relied on by the PWD for assistance in activities of daily living (instrumental or basic).
    • Volunteers (i.e. "Companion Guides") are eligible if:
  • English-speaking,
  • 55 years or older, (3) High School diploma or General Equivalency Diploma (GED) (minimum) (2) ability pass a basic adult literacy screen
  • Ability to pass a background check, physical and mental health screening,
  • A Montreal Cognitive Assessment (MoCA)-Blind score of 18 or above,
  • Ability to commit to 12 months of service (5 hours per week, excluding travel time and continuing education and support), and
  • Are reliable during intake and on-boarding process and able to successfully complete training.

Age in the registry: 18 years to 115 years · 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
Johns Hopkins University
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status

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