Ignite Creation Date:
2024-05-06 @ 1:52 PM
Last Modification Date:
2024-10-26 @ 1:21 PM
Study NCT ID:
NCT04146545
Status:
COMPLETED
Last Update Posted:
2023-07-10
First Post:
2019-10-29
Brief Title:
CommunityRx-Dementia
Sponsor:
University of Chicago
Organization:
University of Chicago
Study Overview
Official Title:
CommunityRx-Dementia A Study for Primary Caregivers of Loved Ones With Alzheimers Disease and Related Dementias
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
CRx-D
Brief Summary:
Caregivers of home-dwelling people with Alzheimers Disease and related dementias ADRD are one of the most rapidly growing populations in the United States Among ADRD caregivers with unmet health-related social needs this study aims to evaluate the effects of the CRx-D intervention versus usual care on caregiver self-efficacy
Detailed Description:
The CRx-D intervention is a caregiver-centered adaptation of CommunityRx CRx an information-based intervention that systematically matches people to nearby community resources for health-related social needs We are conducting a single-blind randomized controlled trial and enrolling caregivers through UChicago-affiliated clinic sites Caregivers will be screened and asked about unmet health-related social needs at the outpatient visit Eligible self-identified caregivers will complete an in-person baseline survey on-site face to face followed by phone surveys at 7 30 90 days and 12 months Caregivers randomized to the intervention will receive tailored information on community resources for their identified health-related social needs They will also be given access to an online community-resource tool and shown how to use it so they can search for additional resources in their community beyond the point-of-care and outside of the clinic All caregivers regardless of research arm will also receive a series of text messages related to the study such as reminders to schedule the phone survey with a member of the research team
The anticipated sample n414 includes pretest participants n20 RCT participants enrolled in the 12-month RCT n344 and additional men caregivers enrolled in a 3-month RCT N50
The anticipated sample n414 includes pretest participants n20 RCT participants enrolled in the 12-month RCT n344 and additional men caregivers enrolled in a 3-month RCT N50
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 1R01AG064949-01 | NIH | None | httpsreporternihgovquickSearch1R01AG064949-01 |