Ignite Creation Date:
2024-05-06 @ 8:01 PM
Last Modification Date:
2024-10-26 @ 3:19 PM
Study NCT ID:
NCT06225986
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-27
First Post:
2024-01-09
Brief Title:
Living Memory Home-4-Dementia Care Pairs
Sponsor:
Weill Medical College of Cornell University
Organization:
Weill Medical College of Cornell University
Study Overview
Official Title:
The Living Memory Home Reducing Grief and Improving Relationships Between Home-Based Patients With ADRD and Their Family Caregivers
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
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:
LMH-4-DCP
Brief Summary:
The purpose of this study is to evaluate an online platform -- the Living Memory Home for Dementia Care Pairs LMH-4-DCP for persons with dementia and their family caregivers to engage in reminiscence activities together and record meaningful memories
The main aims of this study are
To evaluate the feasibility and acceptability of the LMH-4-DCP platform
To explore the potential for LMH-4-DCP to reduce feelings of pre-loss grief and enhancing relationship quality in dementia family caregivers and their care-recipients Care-Pairs
Care pair participants will be asked to log-in to LMH-4-DCP and complete study activities three times per week for one month Researchers will compare the intervention group to an attention control condition to see if LMH-4-DCPs use is associated with reduced feelings of caregiver pre-loss grief and improved care pair relationship quality at follow-up
The main aims of this study are
To evaluate the feasibility and acceptability of the LMH-4-DCP platform
To explore the potential for LMH-4-DCP to reduce feelings of pre-loss grief and enhancing relationship quality in dementia family caregivers and their care-recipients Care-Pairs
Care pair participants will be asked to log-in to LMH-4-DCP and complete study activities three times per week for one month Researchers will compare the intervention group to an attention control condition to see if LMH-4-DCPs use is associated with reduced feelings of caregiver pre-loss grief and improved care pair relationship quality at follow-up
Detailed Description:
The goal of this randomized controlled trial is to evaluate the Living Memory Home for Dementia Care Pairs LMH-4-DCP web application a dyadic online psychosocial reminiscence platform to reduce feelings of pre-loss grief and improve relationship quality in individuals with dementia and their family caregivers Care Pairs
The main aims of this study are
To evaluate the feasibility and acceptability of the LMH-4-DCP platform
To explore the influence of the LMH-4-DCP intervention on reducing feelings of pre-loss grief and enhancing relationship quality in the care pair
Care pair participants randomized to the intervention condition will be asked to log-iin to LMH-4-DCP and complete reminiscence activities three times per week for one month Researchers will compare the intervention group to an attention control condition which includes LMH-4-DCP use without reminiscence-specific features to see if LMH-4-DCPs use is associated with reduced feelings of caregiver pre-loss grief and improved care pair relationship quality at follow-up
The main aims of this study are
To evaluate the feasibility and acceptability of the LMH-4-DCP platform
To explore the influence of the LMH-4-DCP intervention on reducing feelings of pre-loss grief and enhancing relationship quality in the care pair
Care pair participants randomized to the intervention condition will be asked to log-iin to LMH-4-DCP and complete reminiscence activities three times per week for one month Researchers will compare the intervention group to an attention control condition which includes LMH-4-DCP use without reminiscence-specific features to see if LMH-4-DCPs use is associated with reduced feelings of caregiver pre-loss grief and improved care pair relationship quality at follow-up
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 |
|---|---|---|---|
| R21AG077144 | NIH | None | httpsreporternihgovquickSearchR21AG077144 |