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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06140004
Other study ID # HS-17-00279
Secondary ID 1K99AG052647-015
Status Completed
Phase
First received
Last updated
Start date September 15, 2016
Est. completion date October 31, 2020

Study information

Verified date November 2023
Source University of Southern California
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This research challenges our current approach to fee-for-service palliative care and is significant because it will advance the fields of palliative and person-centered care, clinical practice, public policy, and health care financing. However, the most important effect will be on seriously ill patients and their families through increased access to palliative care outside of hospitals, enhanced palliative continuity across health settings, and improved affordability via reformed payment structures. Nation-wide replication of reimbursable HBCP models is anticipated.


Description:

This study will undertake an effort to address the two-pronged gap in providing palliative care in the U.S. (episodic care and misaligned financing structures). This will be done by implementing an evidence-based Home-Based Palliative Care (HBPC) model-originally developed in managed care-into primary fee-for-service as a covered health benefit; the very first translation of this model by a private health insurer in the U.S. The purpose of the present study is to investigate the provider and organizational-level impact of implementing reimbursable HBPC in primary care with the goal of characterizing a set of implementation strategies and eliciting key mechanisms on how to widely replicate person-centered, reimbursable HBPC in primary care settings across the country. To this end, seven research questions will be answered that address the study purpose pertaining to feasibility, barriers, facilitators, person-centeredness, and job satisfaction. This study is guided by the Diffusion of Innovations theory. The investigators will conduct primary collection and analysis of qualitative focus group data at each study site. Key outcomes for the qualitative component include feasibility, barriers, and facilitators of translating HBPC, as well as characteristics associated with rate of HBPC diffusion and implementation strategies. This project challenges our current approach to fee-for-service palliative care and seeks to shift current research. Nation-wide replication of reimbursable HBCP models is anticipated.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date October 31, 2020
Est. primary completion date June 27, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: • Current member of the Home-Based Palliative Care (HBPC) team or organization's leadership team Exclusion Criteria: - No interaction with palliative care patients or palliative care arm of organization - Unable to speak and read English

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States By the Bay Health Larkspur California
United States Snowline Hospice Sacramento California
United States HavenHealth Signal Hill California

Sponsors (2)

Lead Sponsor Collaborator
University of Southern California National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Confidence in Team Self-reported rating of confidence in HBPC team to implement the intervention as stated, on a scale of 1-10 (1=not confident at all; 10=extremely confident) 12-months
Secondary Confidence in Self Self-reported rating of confidence in self to implement the intervention as stated, on a scale of 1-10 (1=not confident at all; 10=extremely confident) 12-months
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