Testing a training tool for hospice clinicians caring for dementia patients
Study 3. Pilot Testing Feasibility, Acceptability, and Preliminary Efficacy of a Dementia-Enhanced Training and Tool for Home Hospice Clinicians in a Clinical Setting.
This study is testing a new training program for hospice workers to see if it helps them better care for dementia patients and supports their families.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 19 Years to 90 Years |
| Sex | All |
| Sponsor | Rutgers, The State University of New Jersey Academic / other |
| Locations | 1 site (New Brunswick, New Jersey) |
| Trial ID | NCT05719077 on ClinicalTrials.gov |
What this trial studies
This pilot study aims to evaluate the feasibility, acceptability, and preliminary efficacy of a dementia-enhanced training program and tool designed for home hospice clinicians. The study will involve 40 clinicians and 160 family caregivers, comparing those who receive the training to those who do not. Primary outcomes include caregiver burden reduction, while secondary outcomes focus on clinician knowledge and confidence regarding dementia care. The study will also explore the impact on family caregiver preparedness and patient discharge rates.
Who should consider this trial
Good fit: Ideal candidates include family caregivers of individuals living with dementia who are enrolled in home hospice care and identify as either Black or White.
Not a fit: Patients who do not identify as Black or White or are not enrolled in home hospice care may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly reduce caregiver burden and improve the quality of care for patients with dementia in home hospice settings.
How similar studies have performed: Other studies have shown success in enhancing caregiver training and support, indicating potential for positive outcomes in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Participant is less than 19 years old or older than 90 years old. * Does not provide care to person(s) living with dementia enrolled in home hospice. * Cannot complete data collection in English. * Family Caregiver does not identify as White or Black/African American.
Where this trial is running
New Brunswick, New Jersey
- Rutgers Univeristy — New Brunswick, New Jersey, United States (Recruiting)
Study contacts
- Principal investigator: Elizabeth Luth, PhD — Rutgers University
- Study coordinator: Elizabeth Luth, PhD
- Email: eal133@ifh.rutgers.edu
- Phone: 646-512-0670
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.