Purpose

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 two weeks. Researchers will compare the intervention group to an attention control condition to see if LMH-4-DCP's use is associated with reduced feelings of caregiver pre-loss grief and improved care pair relationship quality at follow-up.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

Family Caregivers: - be a primary source of care for a family member in the early to moderate stages of dementia - 18 years of age or older - English-speaking - able to use the internet and has internet access - residing in the United States

Exclusion Criteria

Caregiver exclusion criteria: - is not the primary family caregiver of the PwD - under the age of 18-years-old - exhibits cognitive impairment (by scoring 3 or more on the SPMSQ) - does not speak English as a primary language. PwD exclusion criteria: - severe cognitive impairment detected by the clinical or study staff using validated, brief screening tools (e.g., a score of 8 errors or more on the SPMSQ) - does not demonstrate capacity to consent (e.g., a score of 9 or fewer errors on the University of California-San Diego Brief Assessment of Capacity to consent - PwD is living in a long-term care facility - does not speak English as a primary language - is under the age of 18 years old.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Supportive Care
Masking
Single (Participant)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
LMH-4-DCP Intervention
  • Behavioral: LMH-4-DCP
    Reminiscence-based intervention for family caregiver-Persons with Dementia (PwD) dyads to record and reflect on meaningful memories to address family caregivers' pre-loss grief and enhance relationship quality.
Active Comparator
Attention Control Arm
  • Behavioral: LMH-4-DCP access without reminiscence activities
    Participants in the attention control condition will have access to a version of LMH-4-DCP excluding reminiscence-specific activities.

Recruiting Locations

Weill Cornell Medicine
New York, New York 10021
Contact:
Sydney C Saviano, B.A
sys4002@med.cornell.edu

More Details

NCT ID
NCT06225986
Status
Recruiting
Sponsor
Weill Medical College of Cornell University

Study Contact

Sydney C Saviano, B.A.
646-962-5637
sys4002@med.cornell.edu

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 Caregiver participants randomized to the intervention condition will be asked to log-in to LMH-4-DCP and complete reminiscence activities three times per week for two weeks. 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-DCP's use is associated with reduced feelings of caregiver pre-loss grief and improved care pair relationship quality at follow-up.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.