Trial Outcomes & Findings for MEMORI Corps: Activity-based Companion Care for Dementia (NCT NCT03896711)

NCT ID: NCT03896711

Last Updated: 2026-01-28

Results Overview

The total score (frequency x severity) of the Neuropsychiatric Inventory (NPI) scale will be used to measure neuropsychiatric and behavioral symptoms. The NPI is a proxy rating of person with dementia's severity, frequency, and distress across 12 types of neuropsychiatric behavior problems. Scores can range from 0-144, with higher score indicating greater neuropsychiatric behavioral burden.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

175 participants

Primary outcome timeframe

Baseline - 12 weeks

Results posted on

2026-01-28

Participant Flow

Overall, we received over 650 community-based referrals from over 20 unique community-based referral sources (including health care and non-health care related sources).

Completed enrollment of 175 individual participants. 173 were randomized (61 Persons Living With Dementia (PLWD), 61 Family Caregivers, 51 Volunteer/Companion Guides). 1 dyad was inadvertently not randomized after baseline and excluded from analysis.

Participant milestones

Participant milestones
Measure
Active Intervention
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Overall Study
STARTED
90
83
Overall Study
PLWD
33
28
Overall Study
Family Caregivers
33
28
Overall Study
Volunteer/Companion Guides
24
27
Overall Study
COMPLETED
72
70
Overall Study
NOT COMPLETED
18
13

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Active Intervention
n=90 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained volunteers 55 years and older, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests. Delivered virtually by Zoom.
Control
n=83 Participants
Augmented waitlist control. Augmented Waitlist Control: Participants living with dementia/caregivers will continue any services and supports thy are already engaged with, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"), a Resource Guide (ie.,local, regional and national resources), and check-in calls to answer any questions about the materials. Waitlist are offered full intervention after waitlist period. Volunteers randomized to waitlist control continue their usual activities (volunteer or other), and resource a resource guide on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Total
n=173 Participants
Total of all reporting groups
Age, Categorical
Persons living with dementia · <=18 years
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Persons living with dementia · Between 18 and 65 years
5 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
3 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
8 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Persons living with dementia · >=65 years
28 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
25 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
53 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Dementia Caregivers · <=18 years
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Dementia Caregivers · Between 18 and 65 years
11 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
12 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
23 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Dementia Caregivers · >=65 years
22 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
16 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
38 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Volunteer Companion Guides · <=18 years
0 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Volunteer Companion Guides · Between 18 and 65 years
10 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
12 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
22 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Categorical
Volunteer Companion Guides · >=65 years
14 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
15 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
29 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Continuous
Persons living with dementia
78.03 years
STANDARD_DEVIATION 8.95 • n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
75.46 years
STANDARD_DEVIATION 8.50 • n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
76.85 years
STANDARD_DEVIATION 8.77 • n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Continuous
Dementia Caregivers
69.18 years
STANDARD_DEVIATION 9.12 • n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
64.64 years
STANDARD_DEVIATION 9.99 • n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
67.10 years
STANDARD_DEVIATION 9.72 • n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Age, Continuous
Volunteer Companion Guides
66.58 years
STANDARD_DEVIATION 7.78 • n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
65.78 years
STANDARD_DEVIATION 8.17 • n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
66.16 years
STANDARD_DEVIATION 7.92 • n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Sex: Female, Male
Person Living with Dementia · Female
13 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
13 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
26 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Sex: Female, Male
Person Living with Dementia · Male
20 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
15 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
35 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Sex: Female, Male
Dementia Caregiver · Female
25 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
23 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
48 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Sex: Female, Male
Dementia Caregiver · Male
8 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
5 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
13 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Sex: Female, Male
Volunteer Companion Guide · Female
22 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
23 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
45 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Sex: Female, Male
Volunteer Companion Guide · Male
2 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
4 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
6 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · American Indian or Alaska Native
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · Asian
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · Native Hawaiian or Other Pacific Islander
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · Black or African American
11 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
11 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
22 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · White
22 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
17 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
39 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · More than one race
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Person Living with Dementia · Unknown or Not Reported
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · American Indian or Alaska Native
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · Asian
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · Native Hawaiian or Other Pacific Islander
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · Black or African American
11 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
12 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
23 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · White
22 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
14 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
36 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · More than one race
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Dementia Caregiver · Unknown or Not Reported
0 Participants
n=33 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=28 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=61 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · American Indian or Alaska Native
0 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · Asian
0 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · Native Hawaiian or Other Pacific Islander
0 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · Black or African American
8 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
3 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
11 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · White
14 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
22 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
36 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · More than one race
2 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
1 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
3 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Race (NIH/OMB)
Volunteer Companion Guide · Unknown or Not Reported
0 Participants
n=24 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=27 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
0 Participants
n=51 Participants • The total participant sample is comprised of 3 subgroups of participants (Persons living with Dementia, Caregivers, and Volunteer Companion Guides) and these have been represented separately in rows.
Neuropsychiatric Inventory (NPI) Score
21.80 units on a scale
STANDARD_DEVIATION 19.36 • n=33 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
17.38 units on a scale
STANDARD_DEVIATION 14.79 • n=28 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
19.51 units on a scale
STANDARD_DEVIATION 19.50 • n=61 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
Leisure Activity Participation Impact Scale
42.21 units on a scale
STANDARD_DEVIATION 7.51 • n=33 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
40.45 units on a scale
STANDARD_DEVIATION 5.47 • n=28 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
41.66 units on a scale
STANDARD_DEVIATION 6.80 • n=61 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
Quality of Life in Alzheimer's Disease (QOL-AD)
33.54 units on a scale
STANDARD_DEVIATION 6.29 • n=33 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
31.22 units on a scale
STANDARD_DEVIATION 4.01 • n=28 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
32.67 units on a scale
STANDARD_DEVIATION 5.78 • n=61 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
Zarit Burden Inventory-Short Form
16.51 units on a scale
STANDARD_DEVIATION 7.70 • n=33 Participants • This baseline measure is for a subset of participants (i.e., Caregivers of persons living with dementia-CGs). Excludes persons living with dementia and senior volunteer companion guide participants.
19.56 units on a scale
STANDARD_DEVIATION 6.57 • n=28 Participants • This baseline measure is for a subset of participants (i.e., Caregivers of persons living with dementia-CGs). Excludes persons living with dementia and senior volunteer companion guide participants.
17.72 units on a scale
STANDARD_DEVIATION 7.36 • n=61 Participants • This baseline measure is for a subset of participants (i.e., Caregivers of persons living with dementia-CGs). Excludes persons living with dementia and senior volunteer companion guide participants.
Patient Health Questionnaire (PHQ) - 8
4.08 units on a scale
STANDARD_DEVIATION 4.49 • n=33 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
4.18 units on a scale
STANDARD_DEVIATION 5.03 • n=28 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
4.14 units on a scale
STANDARD_DEVIATION 4.69 • n=61 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
UCLA 3 Loneliness Scale
4.65 units on a scale
STANDARD_DEVIATION 1.80 • n=33 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
4.05 units on a scale
STANDARD_DEVIATION 1.60 • n=28 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
4.36 units on a scale
STANDARD_DEVIATION 1.69 • n=61 Participants • This baseline measure is for a subset of participants (i.e., persons living with dementia, PWD). Excludes caregiver and senior volunteer companion guide participants.
Caregiver UCLA 3 Loneliness Scale
4.71 units on a scale
STANDARD_DEVIATION 1.82 • n=33 Participants • This baseline measure is for a subset of participants (i.e., caregivers of persons living with dementia). Excludes persons living with dementia and senior volunteer companion guide participants.
5.00 units on a scale
STANDARD_DEVIATION 1.72 • n=28 Participants • This baseline measure is for a subset of participants (i.e., caregivers of persons living with dementia). Excludes persons living with dementia and senior volunteer companion guide participants.
4.81 units on a scale
STANDARD_DEVIATION 1.77 • n=61 Participants • This baseline measure is for a subset of participants (i.e., caregivers of persons living with dementia). Excludes persons living with dementia and senior volunteer companion guide participants.
Caregiver Time Spent Helping PLWD in Last Week
50.84 hours per week
STANDARD_DEVIATION 47.07 • n=33 Participants • This baseline measure is for a subset of participants (i.e., caregivers of PWD). Excludes person with dementia (PWD) and senior volunteer companion guide participants.
49.48 hours per week
STANDARD_DEVIATION 43.38 • n=28 Participants • This baseline measure is for a subset of participants (i.e., caregivers of PWD). Excludes person with dementia (PWD) and senior volunteer companion guide participants.
50.22 hours per week
STANDARD_DEVIATION 45.04 • n=61 Participants • This baseline measure is for a subset of participants (i.e., caregivers of PWD). Excludes person with dementia (PWD) and senior volunteer companion guide participants.
Senior Companion Volunteers Patient Health Questionnaire (
1.54 units on a scale
STANDARD_DEVIATION 1.61 • n=24 Participants • This baseline measure is for a subset of participants (i.e., senior volunteer companion guide participants). Excludes persons living with dementia and caregiver participants.
1.46 units on a scale
STANDARD_DEVIATION 1.88 • n=27 Participants • This baseline measure is for a subset of participants (i.e., senior volunteer companion guide participants). Excludes persons living with dementia and caregiver participants.
1.49 units on a scale
STANDARD_DEVIATION 1.71 • n=51 Participants • This baseline measure is for a subset of participants (i.e., senior volunteer companion guide participants). Excludes persons living with dementia and caregiver participants.

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Person with dementia participant outcome, intent to treat

The total score (frequency x severity) of the Neuropsychiatric Inventory (NPI) scale will be used to measure neuropsychiatric and behavioral symptoms. The NPI is a proxy rating of person with dementia's severity, frequency, and distress across 12 types of neuropsychiatric behavior problems. Scores can range from 0-144, with higher score indicating greater neuropsychiatric behavioral burden.

Outcome measures

Outcome measures
Measure
Active Intervention
n=26 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=19 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Neuropsychiatric Symptoms as Assessed by Neuropsychiatric Inventory (NPI) Score
3.35 score on a scale
Standard Deviation 11.14
0.47 score on a scale
Standard Deviation 6.10

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Person with dementia participant outcome, intent to treat

The total score (sum of all items) for the Quality of life in Alzheimer's Disease (QOL-AD) tool will assess quality of life in the context of Alzheimer's Disease. The QOL-AD has a self-rated and proxy-rated version for persons with dementia, and was specifically developed for use in dementia. Scores can range from 13-52, with higher scores indicating better quality of life.

Outcome measures

Outcome measures
Measure
Active Intervention
n=19 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=18 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Quality of Life as Assessed by the Quality of Life in Alzheimer's Disease (QOL-AD) Tool
0.21 units on a scale
Standard Deviation 3.44
-0.44 units on a scale
Standard Deviation 4.97

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Caregivers of persons with dementia participants, Intent to treat

The total score (sum of items) for the Zarit Burden Inventory-Short Form-12 items (ZBI) will assess subjective caregiver burden. The ZBI short form is a self-rated 12-item measure of caregiver subjective burden rating related to caregiving for persons with dementia. Scores can range from 0-48, with higher scores indicating greater perceived burden.

Outcome measures

Outcome measures
Measure
Active Intervention
n=26 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=23 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Subjective Caregiver Burden as Assessed by the Zarit Burden Inventory-Short Form
0.04 units on a scale
Standard Deviation 4.84
-0.69 units on a scale
Standard Deviation 5.84

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Caregiver of person living with dementia outcome, intent to treat

The total score (sum of items) for the The Patient Health Questionnaire (PHQ) - 8 will assess depressive symptoms severity. The PHQ-8 is a self-rated 8 item measure of caregiver depressive symptoms. Scores can range from 0-24, with higher scores indicating greater depressive symptoms.

Outcome measures

Outcome measures
Measure
Active Intervention
n=26 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=22 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Depressive Symptoms in Caregivers as Assessed by The Patient Health Questionnaire (PHQ) - 8
0.38 units on a scale
Standard Deviation 3.97
0.59 units on a scale
Standard Deviation 2.97

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Person living with dementia participant outcome, intent to treat

Three item measure of perceived loneliness and social isolation. Scores range from 3-9 with higher scores indicating higher levels of loneliness.

Outcome measures

Outcome measures
Measure
Active Intervention
n=15 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=19 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Perceived Loneliness as Measured by UCLA 3 Loneliness Scale
0.20 units on a scale
Standard Deviation 1.86
-0.42 units on a scale
Standard Deviation 1.07

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Caregiver of person with dementia outcome, intent to treat

Three item measure of perceived loneliness and social isolation. Scores range from 3-9 with higher scores indicating higher levels of loneliness.

Outcome measures

Outcome measures
Measure
Active Intervention
n=23 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=20 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Perceived Loneliness for Caregiver as Measured by UCLA 3 Loneliness Scale
-0.39 units on a scale
Standard Deviation 1.23
0.10 units on a scale
Standard Deviation 1.71

PRIMARY outcome

Timeframe: 12-weeks post intervention

Population: caregivers in intervention arm only of persons with dementia receiving intervention, intent to treat

55 item likert scale survey assessing program delivery, feasibility, acceptability, perceived program impact. Total score range from 55-253 with higher scores indicating greater satisfaction and perceived feasibility, with higher scores indicating

Outcome measures

Outcome measures
Measure
Active Intervention
n=26 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Program Satisfaction and Perceived Impact Survey
124.15 score on a scale
Standard Deviation 25.20

PRIMARY outcome

Timeframe: Baseline - 12 weeks

Population: Person living with dementia participant outcome, intent to treat

11 item scale measuring the subjective impact of leisure activity participation on several areas of life and emotional well-being. Scores range from 11-55 with higher scores indicating more beneficial subjective impact of leisure activities

Outcome measures

Outcome measures
Measure
Active Intervention
n=21 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=16 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Perceived Impact of Leisure Activities as Measured by Leisure Activity Participation Impact Scale
-1.71 score on a scale
Standard Deviation 4.01
-1.63 score on a scale
Standard Deviation 4.46

SECONDARY outcome

Timeframe: Baseline - 12 weeks

Population: caregiver of person living with dementia participant outcomes, intent to treatment

Two individual items ask caregivers to estimate hours per day spent doing caregiving activities, and hours per day spent with the person with dementia in a typical week. Objective measure of caregiver burden. Higher time estimates in performing these tasks indicate greater objective burden.

Outcome measures

Outcome measures
Measure
Active Intervention
n=26 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=23 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Caregiver Time Spent Helping Person Living With Dementia
-14.04 hours per week
Standard Deviation 45.56
-0.96 hours per week
Standard Deviation 29.37

SECONDARY outcome

Timeframe: Baseline -12 weeks

Population: Outcome is only for senior companion guide volunteer participants, intent to treat. This outcome is for a subset of participants (i.e., senior volunteer companion guides). Excludes PLWD and caregiver participants.

The total score (sum of items) for the The Patient Health Questionnaire (PHQ) - 8 will assess depressive symptoms severity in senior companion volunteers. The PHQ-8 is a self-rated 8 item measure of caregiver depressive symptoms. Scores can range from 0-24, with higher scores indicating greater depressive symptoms.

Outcome measures

Outcome measures
Measure
Active Intervention
n=24 Participants
Intervention arm with MEMORI Corps program MEMORI Corps program: Virtual activity-based companion care program. Delivered by trained senior volunteers, supported by a clinical team, over a 12-week intervention period (up to 5 hours per week, one or more days per week) for each person with dementia/family caregiver dyad. Primary roles of the volunteers are to provide socialization, companionship, and a personalized activity program that focuses on meaningful, engaging and enjoyable activities that match the participant's abilities and interests.
Control
n=27 Participants
Augmented waitlist control. Augmented Waitlist Control: Persons with dementia/caregivers will continue any services and supports being used, will receive a free copy of "A Caregiver's Guide to Dementia: Using Activities and Other Strategies to Prevent, Reduce and Manage Behavioral Symptom"103), a Resource Guide with written educational materials on local, regional and national resources, management of CG stress/well-being, and check-in calls to answer any questions about the materials. Volunteers randomized to waitlist control will continue with usual activities (volunteer or other), and will receive additional written educational materials on cognitive health (NIA) and exercise and Physical Activity (Go4Life), referrals to the Baltimore City Commission on Aging and Retirement Education for volunteering opportunities, and check-in calls to answer questions and maintain engagement. Waitlist dyads will be followed at specified intervals by the research team and then offered an opportunity for participation in the intervention arm.
Change in Depressive Symptoms in Senior Companion Volunteers as Assessed by The Patient Health Questionnaire (PHQ) - 8
1.02 units on a scale
Standard Deviation 2.61
0.80 units on a scale
Standard Deviation 1.79

Adverse Events

Active Intervention-PLWD

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Active Intervention - Volunteer/Companion Guides

Serious events: 0 serious events
Other events: 0 other events
Deaths: 1 deaths

Waitlist Control - PLWD

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Waitlist Control - Volunteer/Companion Guides

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Waitlist Received Intervention - PLWD

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Waitlist Received Intervention - Volunteer/Companion Guides

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Quincy Samus, Professor

Johns Hopkins University

Phone: 4105506493

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place