Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Tests a self-care program for caregivers of adults with heart failure and memory problems

Tests a behavioral program for family caregivers of adults with heart failure and cognitive impairment.

Plain-language title generated from the registry record
Registry title: Improving Self-Care of Caregivers of Adults in Homecare With Heart Failure and Cognitive Impairment

Key facts

Where
New York, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 101 years old?

Source: NCT07220798, who can take part

Where in United States

  • VNS HealthNew York, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Visiting Nurse Service of New York
Trial code
NCT07220798
Record updated
12 August 2026
Original description
This RCT design will enroll 256 informal caregivers (spouse/partner or child) of HHC patients with HF/CI and 60 patients with HF and mild to moderate CI (60 dyads). After collecting baseline data, we will block randomize the caregivers 1:1 to the ViCCY intervention or comparator group, stratifying randomization by caregiver sex (male/female), relationship (spouse/partner or child), and race (white/other)- factors known to influence caregiving burden, perceived stress, and receptivity to the intervention. We will encourage caregivers to use their own devices but provide tablet devices with wireless network access if needed. The intervention group will receive 10 sessions of ViCCY over 6 months.Read full original descriptionShow less

Improving Self-Care of Caregivers of Adults in Homecare With Heart Failure and Cognitive Impairment (iCare4Me Homecare)

This RCT design will enroll 256 informal caregivers (spouse/partner or child) of HHC patients with HF/CI and 60 patients with HF and mild to moderate CI (60 dyads). After collecting baseline data, we will block randomize the caregivers 1:1 to the ViCCY intervention or comparator group, stratifying randomization by caregiver sex (male/female), relationship (spouse/partner or child), and race (white/other)- factors known to influence caregiving burden, perceived stress, and receptivity to the intervention. We will encourage caregivers to use their own devices but provide tablet devices with wireless network access if needed. The intervention group will receive 10 sessions of ViCCY over 6 months.

Inclusion: Patient Inclusion Criteria; Older adults (=>50 years of age); Enrolled in Home Health Care; Documented to have HF; Mild to moderate CI on the BIMS or OASIS items; Able to provide informed consent; Able to provide self-report data; Caregiver Inclusion Criteria; Adults (=>18 years of age); Spouse/partner/child or other informal caregiver living with or in close proximity to the patient; Caregiver of a home care patient who is currently receiving or recently received services and who has mild to severe cognitive impairment; Reporting poor self-care on screening (Health Self-Care Neglect scale score =>2); Reporting poor mental health on screening (screened with the PROMIS Global Mental Health 4a score <12); Caregiving or supporting the patient at least 8 hours/week; Able to complete the protocol, e.g., adequate vision and hearing, English speaking; Able to provide informed consent; Able to use technology.

Exclusion: Patient Exclusion Criteria; Dementia (ICD-10 code for dementia); Enrolled in hospice; Non-English speaking; Caregiver Exclusion Criteria 1. Non-English speaking.

ClinicalTrials.gov NCT07220798