ClinicalTrials.Veeva

Menu

Dementia Care Partner Hospital Assessment Tool

University of Wisconsin (UW) logo

University of Wisconsin (UW)

Status

Enrolling

Conditions

Alzheimer Disease
Dementia

Treatments

Behavioral: Care Partner Hospital Assessment Tool

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05592366
Protocol Version 12/28/2022 (Other Identifier)
A176000 (Other Identifier)
1K23AG080068-01 (U.S. NIH Grant/Contract)
2022-0352
EDUC/KINESIOLOGY (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to see whether an adapted questionnaire called the Care Partner Hospital Assessment Tool (CHAT) for care partners of hospitalized patients living with Alzheimer's disease and related dementias (ADRD) (CHAT-AD) can help people with dementia receive better care after they go home from the hospital. Participants will be a care partner ('family member or friend') who provides unpaid care to a hospitalized adult relative or partner to help them take care of themselves because of dementia. Participants can expect to be in this study for 14 days.

Full description

The purpose of this study is to adapt CHAT for care partners of hospitalized patients living with ADRD (CHAT-AD) and evaluate its feasibility and potential efficacy in a pilot randomized clinical trial. Findings from this study will enable the lead researcher to launch an independent program of research that aims to (1) improve hospital-based care processes and outcomes for patients living with ADRD and their care partners, and (2) make clear the essential caregiving role that so many care partners of patients living with ADRD assume.

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.

Enrollment

128 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Provide unpaid care to a hospitalized adult relative or partner to help them take care of themselves because of ADRD
  • 18 years or older

Exclusion criteria

  • Non-English speaking

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

128 participants in 2 patient groups

Standard of Care
No Intervention group
Description:
Participants in this arm will only receive standard of care.
Adjusted CHAT-AD
Experimental group
Description:
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.
Treatment:
Behavioral: Care Partner Hospital Assessment Tool

Trial contacts and locations

1

Loading...

Central trial contact

Anne Mortensen

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems