Ignite Creation Date:
2024-05-06 @ 6:35 PM
Last Modification Date:
2024-10-26 @ 2:51 PM
Study NCT ID:
NCT05719077
Status:
RECRUITING
Last Update Posted:
2024-05-09
First Post:
2023-01-20
Brief Title:
Pilot Testing Dementia-Enhanced Training and Tool for Home Hospice Clinicians
Sponsor:
Rutgers The State University of New Jersey
Organization:
Rutgers The State University of New Jersey
Study Overview
Official Title:
Study 3 Pilot Testing Feasibility Acceptability and Preliminary Efficacy of a Dementia-Enhanced Training and Tool for Home Hospice Clinicians in a Clinical Setting
Status:
RECRUITING
Status Verified Date:
2024-05
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:
EDITH-HC
Brief Summary:
The purpose of this study is to pilot test the feasibility acceptability and preliminary efficacy of a clinically useful inclusive dementia-enhanced training and tool for use by home hospice clinicians to improve care and support for Black and White patients with dementia and their family caregivers The investigators expect family caregivers of clinicians in the intervention group will report less caregiver burden primary outcome than caregivers of clinicians in the control group The investigators expect that compared to clinicians in the control group usual care clinicians in the intervention group receive the training and use the tool will demonstrate more knowledge of dementia-related caregiving issues secondary outcomes In exploratory analyses the investigators expect family caregivers will report greater self-efficacy and preparedness and that patients of clinicians in the intervention group will experience fewer live discharges than family caregivers of patients of clinicians in the control group
Detailed Description:
For this aim the investigators will conduct a randomized pilot study to determine the feasibility and acceptability of implementing the training and tool in clinical practice compared to usual care with 40 clinicians 20 intervention 20 control and 160 Black and white FCG 80 intervention 80 control The investigators will also determine preliminary efficacy of the training and tool Outcomes include feasibility and acceptability of the intervention reducing FCG burden primary outcome improving clinician knowledge and confidence secondary outcomes and increasing FCG preparedness and self-efficacy
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 |
|---|---|---|---|
| R00AG065624 | NIH | None | httpsreporternihgovquickSearchR00AG065624 |