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A Study to Evaluate Caregiver Connections Via Technology for Patients With Alzheimer's and Other Types of Dementia

Fostering Caregiver Connections Via Intentional Technology Pairing for Caregivers of Patients With Alzheimer's Disease and Other Types of Dementia-Phase 2

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05497817
Enrollment
0
Registered
2022-08-11
Start date
2022-09-30
Completion date
2024-12-31
Last updated
2022-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiver Stress, Dementia, Alzheimer Dementia, Lewy Body Dementia, Parkinson Disease Dementia, Frontotemporal Dementia

Brief summary

This research is being done to develop a unique matching process for caregivers of persons living with dementia, such as Alzheimer's disease, Lewy body dementia, frontotemporal degeneration, or other dementia syndromes. Dementia caregivers often assume greater caregiving burden than do non-dementia caregivers, and the caregiving duration tends to be longer. Many caregivers do not have the adequate support they need. Peer-to-peer support has been shown to improve quality of life, increase use of services, improve caregiver health, and reduce hospitalizations in the person they are caring for. This study will assess a technology platform and matching process for the purpose of peer-to-peer emotional support aimed at improving overall wellbeing in dementia care partners/caregivers.

Interventions

BEHAVIORALAlgorithm

Current and/or former Care Partners of persons with dementia will be matched using an algorithm to other Care Partners who might provide emotional support.

BEHAVIORALRandom Match

Current and/or former Care Partners of persons with dementia will be randomly matched to other Care Partners who might provide emotional support.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
Minnesota HealthSolutions
CollaboratorINDUSTRY
Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Intervention model description

Participants will be randomly assigned to two different arms of the study: one where the algorithm matches individuals and one where matches are randomly assigned.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Individuals in a current or former caregiving role for a family member living with dementia will be recruited for this study. There will be no sex or gender restrictions, or exclusion based on race or ethnicity. Participants must be at least 18 years of age. Inclusion Criteria: * The participant must have a family member that has been diagnosed with dementia. * The participant must identify as a Care Partner or Caregiver who has contact with their loved one with dementia, in person or by phone, and who provides social/emotional support and full or partial assistance with daily activities at least 3 days per week. * The participant must have been caring for their loved one with dementia for at least 3 months. * All participants must have access to a computer and be able to use the internet. * All participants must be English speaking. * All participants must agree to participate in the 15-month study, which includes completing questionnaires, brief virtual interactions with the study coordinator quarterly, and actively interacting with the website and potential matches. * All participants must agree to follow-up contact throughout the duration of the study, which is anticipated to last 3 years.

Exclusion criteria

* Care Partner's loved one does not have a confirmed diagnosis of dementia. * Care Partner is unable to provide consent. * Care Partner was or has been in that role for less than 3 months.

Design outcomes

Primary

MeasureTime frameDescription
Match Satisfaction Questionnaire12 monthsAll participants will complete a match satisfaction questionnaire to assess whether being matched to a supportive Care Partner via an algorithm based on personal preferences results in greater match satisfaction than being matched at random.
Change over time from Baseline Resilience to 12 monthsBaseline,12 monthsAll participants will complete questions surveying resilience to determine whether Care Partners randomized to algorithmic matching based on personal preferences will report a greater sense of resiliency after being matched than Care Partners who are randomly matched.
Change over time from Baseline Quality of Life to 12 monthsBaseline, 12 monthsAll participants will complete questions surveying quality of life to determine whether Care Partners randomized to algorithmic matching based on personal preferences will report improved quality of life after being matched than Care Partners who are randomly matched.
Scale of Perceived Social Support12 monthsAll participants will complete survey questions regarding perceived level of social support to assess impact on match satisfaction.

Secondary

MeasureTime frameDescription
Survey of Executive Skills12 monthsAll participants will complete questions regarding executive functioning (e.g., flexibility, problem-solving) to determine whether the level of these skills relates to ease or difficulty in finding a satisfactory supportive Care Partner match.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026