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NCT05719077Completed

Pilot Testing Dementia-Enhanced Training and Tool for Home Hospice Clinicians

Study 3. Pilot Testing Feasibility, Acceptability, and Preliminary Efficacy of a Dementia-Enhanced Training and Tool for Home Hospice Clinicians in a Clinical Setting.

Source: ClinicalTrials.gov · Last updated 16 Jul 2026

Brief summary (registry, in English)

The purpose of this study is to pilot test the feasibility, acceptability, and preliminary efficacy of a clinically useful, inclusive dementia-enhanced training and tool for use by home hospice clinicians to improve care and support for Black and White patients with dementia and their family caregivers. The investigators expect family caregivers of clinicians in the intervention group will report less caregiver burden (primary outcome) than caregivers of clinicians in the control group. The investigators expect that, compared to clinicians in the control group (usual care), clinicians in the intervention group (receive the training and use the tool) will demonstrate more knowledge of dementia-related caregiving issues (secondary outcomes). In exploratory analyses, the investigators expect family caregivers will report greater self-efficacy and preparedness, and that patients of clinicians in the intervention group will experience fewer live discharges than family caregivers of patients of clinicians in the control group.

Status (registry)
Completed
Study type
Interventional
Enrollment
93 (actual)
First submitted
20 Jan 2023
Start date
6 Oct 2023
Primary completion date
30 Jun 2025
Lead sponsor
Rutgers, The State University of New Jersey
NCT number
NCT05719077

What you commit to

  • Study type: Interventional
  • Participants enrolled: 93
  • From 6 Oct 2023 to the primary completion date, 30 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Does not provide care to person(s) living with dementia enrolled in home hospice.

Age

  • Participant is less than 19 years old or older than 90 years old.

Other

  • Cannot complete data collection in English.
  • Family Caregiver does not identify as White or Black/African American.

Who the study is looking for

  • Individuals are not excluded from this study based on gender.
  • Based on proportion of hospice workforce and family caregivers that are female, we expect 70%-80% of participants will be female.
  • Nurse, social worker, or family member who provides care to persons(s) living with dementia enrolled in home hospice care.
  • 19-90 years old.
  • Can complete data collection in English.
  • Family Caregivers: identify as White or Black/African American.

Age in the registry: 19 years to 90 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Rutgers Univeristy
Coordinator of this site? Confirm its status
New BrunswickUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.