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Living Memory Home-4-Dementia Care Pairs (LMH-4-DCP)

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status

Enrolling

Conditions

Dyadic Family Caregiver-person With Dementia Online Intervention

Treatments

Behavioral: LMH-4-DCP
Behavioral: LMH-4-DCP access without reminiscence activities

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06225986
R21AG077144 (U.S. NIH Grant/Contract)
23-07026251

Details and patient eligibility

About

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.

Full 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.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

LMH-4-DCP Intervention
Experimental group
Treatment:
Behavioral: LMH-4-DCP
Attention Control Arm
Active Comparator group
Treatment:
Behavioral: LMH-4-DCP access without reminiscence activities

Trial contacts and locations

1

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Central trial contact

Sydney C Saviano, B.A.

Data sourced from clinicaltrials.gov

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