Social Reminder System for Memory Loss

HW
Overseen ByHannah Wheeler
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Minnesota
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This study will evaluate the Social Reminder System, a mobile informatics system designed to support persons with memory concerns and their care partners. The system is intended to aid social integration for persons with memory concerns and improve care coordination and reduce caregiver burden among caregivers.

Researchers will enroll 100 persons with memory concerns and their care partners. Half of the dyads will be randomly assigned to receive the Social Reminder System technology for a 6-month period, and the other half will be randomly assigned to the usual care control group. Participants will complete baseline, 3-month, and 6-month surveys. A subset of participants who receive the technology will also be asked to complete a semi-structured interview after the 6-month survey.

Who Is on the Research Team?

JM

Jude Mikal, PhD

Principal Investigator

University of Minnesota

Are You a Good Fit for This Trial?

This trial is for adults with memory problems, such as mild cognitive impairment or dementia, and their caregivers. Both the person with memory concerns and their care partner must be willing to participate together.

Inclusion Criteria

Care partners of persons with memory concerns must speak English
Care partners must self-identify as the primary caregiver for the person with memory concerns
My care partner is willing to use the Social Reminder System and join any study group.
See 7 more

Exclusion Criteria

Those who do not meet the inclusion criteria will be excluded
Persons with memory concerns with severe or no dementia are not eligible
Individuals who score below 6 and above 24 on the TICS-40 will not be eligible

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Baseline Assessment

Participants complete baseline surveys before exposure to the intervention or attention control

1 week
1 visit (in-person or virtual)

Intervention

Dyads receive the Social Reminder System technology or usual care control for a 6-month period

6 months
Baseline, 3-month, and 6-month surveys

Follow-up

Participants complete follow-up surveys and semi-structured interviews to assess the impact of the intervention

1 month
1 visit (in-person or virtual)

What Are the Treatments Tested in This Trial?

Interventions

  • Social Reminder System

Trial Overview

The study tests a mobile app called the Social Reminder System, which helps people with memory issues stay socially engaged and supports caregivers in managing care. Participants are randomly assigned to use the app or continue usual care for 6 months.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Social Reminder SystemExperimental Treatment1 Intervention
Group II: Usual Care ControlActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Minnesota

Lead Sponsor

Trials
1,459
Recruited
1,623,000+

National Institute on Aging (NIA)

Collaborator

Trials
1,841
Recruited
28,150,000+