Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
128 participants
INTERVENTIONAL
2024-04-02
2027-05-31
Brief Summary
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Detailed Description
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In order to adapt CHAT, there will be two design teams with key stakeholders from local aging networks and a large academic medical system: one team comprised of previously hospitalized patients living with ADRD and their care partners (N=7 dyads) and the second comprised of healthcare system administrators and clinicians (N=7). The team will use a validated participatory human-centered design process in which each team completes 5 co-design videoconference sessions that occur in parallel across 4 months, with 2-3 weeks between each session.
Upon adaptation of the CHAT-AD, the study team will partner with a medical and surgical units that are part of a large academic medical system to recruit 128 eligible care partners of hospitalized patients living with ADRD, randomized into either the CHAT-AD plus usual care or usual care-only groups. The team will assess feasibility by examining overall recruitment, attrition, safety, adherence, and implementation satisfaction. To examine efficacy, a validated measure of caregiving preparedness will be obtained pre- and post-intervention.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Standard of Care
Participants in this arm will only receive standard of care.
No interventions assigned to this group
Adjusted CHAT-AD
Using CHAT, participants will be asked questions about their needs to fully support and care for their loved one after the loved one is released from the hospital.
Care Partner Hospital Assessment Tool
Complete the adjusted CHAT as well as demographic and caregiving questionnaires during and after loved one's hospitalization.
Interventions
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Care Partner Hospital Assessment Tool
Complete the adjusted CHAT as well as demographic and caregiving questionnaires during and after loved one's hospitalization.
Eligibility Criteria
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Inclusion Criteria
* 18 years or older
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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National Institute on Aging (NIA)
NIH
University of Wisconsin, Madison
OTHER
Responsible Party
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Principal Investigators
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Beth Fields, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Wisconsin, Madison
Locations
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University of Wisconsin
Madison, Wisconsin, United States
Countries
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Central Contacts
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Facility Contacts
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References
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Fields B, Werner N, Shah MN, Hetzel S, Golden BP, Gilmore-Bykovskyi A, Farrar Edwards D. Adapting and Testing the Care Partner Hospital Assessment Tool for Use in Dementia Care: Protocol for a 2 Sequential Phase Study. JMIR Res Protoc. 2023 Jun 22;12:e46808. doi: 10.2196/46808.
Other Identifiers
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A176000
Identifier Type: OTHER
Identifier Source: secondary_id
EDUC/KINESIOLOGY
Identifier Type: OTHER
Identifier Source: secondary_id
Protocol Version 10/29/2024
Identifier Type: OTHER
Identifier Source: secondary_id
2022-0352
Identifier Type: -
Identifier Source: org_study_id
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