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Friendly volunteers may ease dementia loneliness

NCT ID NCT03896711

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a program called MEMORI Corps, where trained volunteers aged 55+ provide companionship and personalized activities to people with dementia living at home. The program was delivered virtually over 12 weeks. Researchers measured changes in mood, quality of life, and caregiver stress. The goal was to see if this approach is practical and helpful for everyone involved.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
MEMORI Corps program (behavioral intervention: volunteer companionship and personalized activities delivered virtually)
What this could lead to
If successful, this program could offer a low-cost, social way to improve well-being for people with dementia and reduce caregiver burden.
What could go wrong
This was a small pilot study, so results may not apply broadly. The program relies on volunteers and virtual delivery, which may not work for everyone.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

175 people

The number who actually took part.

Started

Mar 2022

Finished

May 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 115 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 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. Exclusion Criteria: PWD are excluded if: * Deemed to be in a crisis/unsafe situation at baseline, * Planned transition from home in less than 6 months, * At end-stage disease (e.g. bed-bound and non-communicative, or hospice), * Currently enrolled in a dementia related clinical trial, or * 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 * Report having an existing cognitive disorder diagnosis by a health provider (e.g., Mild Cognitive Impairment, Alzheimer's disease or other type of dementia).

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Johns Hopkins University

    Baltimore, Maryland, 21205, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.