Skip to main content
Clinical Trials/NCT04074304
NCT04074304
Completed
Not Applicable

Developing and Piloting a Multi-component Technology-based Care Intervention to Address Patient Symptoms and Caregiver Burden in Home Hospice

Weill Medical College of Cornell University1 site in 1 country12 target enrollmentMay 18, 2021
ConditionsHome Hospice

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Home Hospice
Sponsor
Weill Medical College of Cornell University
Enrollment
12
Locations
1
Primary Endpoint
Participants' experience using the intervention as measured by the I-HoME User-centered design questionnaire
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

With the growth of hospice, older adults have the opportunity to receive home-based care aimed at reducing suffering and focusing on quality of life at the end of life. While use of technology and educational videos has yet to be fully developed, structured, and evaluated in home hospice care, it has shown promise to improve care in other settings. Therefore, this study aims to develop and evaluate a multi-component technology-based care intervention, i.e., Improving Home hospice Management of End of life issues through technology (I-HoME), that focuses on assessing and addressing patient symptoms and caregiver burden in the home hospice setting through synchronous live video visits and educational videos. The aim of the first phase of the project is to employ an iterative user-centered design process to develop I-HoME for home hospice patients and their caregivers prior to implementation.

Registry
clinicaltrials.gov
Start Date
May 18, 2021
End Date
November 3, 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Home hospice providers (N=10) and family caregivers (N=10) must be English speaking, 18 years of age or older, not blind, and either providing or receiving home hospice care. Home hospice patients (N=10) must be English speaking, 65 years of age or older, not blind, and enrolled in home hospice care.

Exclusion Criteria

  • Patients with a terminal diagnosis of dementia or patients who have cognitive impairment and unable to sign a written informed consent will be excluded.

Outcomes

Primary Outcomes

Participants' experience using the intervention as measured by the I-HoME User-centered design questionnaire

Time Frame: 1 day

A questionnaire consisting of open ended questions asking participants to provide feedback and their thoughts about the I-HoME intervention. The responses gathered are not scored, but qualitative analysis will be performed to identify issues that will be used to make revisions to the I-HoME intervention before starting phase 2 of the project.

Study Sites (1)

Loading locations...

Similar Trials