ClinicalTrials.Veeva

Menu

Connecting Caregivers with Community Services: the Care Buddy Platform

Duke University logo

Duke University

Status

Not yet enrolling

Conditions

Dementia

Treatments

Device: Care Buddy

Study type

Interventional

Funder types

Other

Identifiers

NCT06817876
2022-309

Details and patient eligibility

About

The study aims to develop a mobile-app (Care Buddy) which will be a one-stop integrated source of information and technology-based solutions for caregivers of people with dementia (PWDs). Study aims to bring caregivers into closer partnerships with the wider ecosystem (e.g., healthcare practitioners, community services, peer support, and care service providers) which will ultimately improve outcomes for both PWDs and their caregivers.

Full description

This is a 5-year study with various stages: 1) proof-of-concept stage to design and develop the Care buddy intervention, 2) proof-of-value stage to assess the feasibility, acceptability and satisfaction with the Care buddy intervention among informal caregivers of PWDs, 3) test-bedding stage to assess the efficacy and cost-effectiveness of the Care buddy intervention versus usual care among informal caregivers of PWDs with help of a multi-centre 2-arm RCT and 4) deployment stage to scale up the intervention at multiple centres across Singapore, monitor its adoption and outcomes and assess any organizational and individual barriers to adoption.

By the end of the proposed five-year project, investigators aim to develop and evaluate the technology as well as achieve widespread adoption among caregivers of PWDs. Investigators want to enable easy access to information, provide decisional and social support, improve the reach and uptake of existing community service providers, and assist with coordination among multiple informal and professional caregivers through the journey of dementia caregiving and into the bereavement phase.

Enrollment

210 estimated patients

Sex

All

Ages

21 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The inclusion criteria for patients are

    1. Singaporean/Permanent residents
    2. Age 21 years of age or older
    3. Main person or one of the main persons involved in making decisions regarding treatment patient receives or responsible for ensuring the well-being of the patient
    4. An active primary caregiver for at least 6 months, and planning to remain the primary caregiver for the next 2 years
    5. Is a family member of the patient with dementia
    6. Can read and write in English
    7. Accessible by telephone to schedule interviews
    8. Has familiarity with use of technology (e.g., computers, tablets, or internet) and is able to complete surveys, forms using digital technology
    9. Intact cognition determined through the Abbreviated Mental Test (AMT) for those who are ≥ 65 years old.
    10. Caregivers who score >=9 on the 6-item Zarit Burden scale

Exclusion criteria

  • Caregivers of patients staying in nursing home or other long-term care facility with no intention of being discharged will not be eligible however, if the patient is admitted to respite care for short/long term duration after being recruited, caregivers can continue to participate.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

210 participants in 2 patient groups

CareBuddy
Experimental group
Description:
Caregivers of person with dementia who will be randomized in this arm will have access to the CareBuddy mobile app on their phone. They will be using this app for 1 year and will be followed up every 2 months.
Treatment:
Device: Care Buddy
Usual care
No Intervention group
Description:
Caregivers of person with dementia who will be randomized in this arm will continue usual care for their loved one. They will be enrolled for 1 year and will be followed up every 2 months.

Trial contacts and locations

1

Loading...

Central trial contact

Chetna Malhotra, MD, MPH

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems