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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05001620
Other study ID # HP-00095001
Secondary ID U54AG063546
Status Completed
Phase N/A
First received
Last updated
Start date August 4, 2021
Est. completion date July 1, 2023

Study information

Verified date July 2023
Source University of Maryland, Baltimore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Grounded in the Reach-Effectiveness-Adoption-Implementation-Maintenance (RE-AIM) Model, this study will assess the implementation outcomes of the Nurse Practitioner (NP) delivered telehealth Palliative Care Consultation in Post-Acute Care (PCC-PAC) intervention for persons living with dementia (PLWD) and their care-partners newly admitted to nursing homes (NHs) for post-acute care.


Description:

This single arm embedded pragmatic pilot clinical trial will provide data to assess the implementation outcomes of the Nurse Practitioner (NP) delivered telehealth Palliative Care Consultation in Post-Acute Care (PCC-PAC) intervention among 30 persons living with dementia (PLWD) and their care-partners newly admitted to one nursing homes (NH) for post-acute care.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date July 1, 2023
Est. primary completion date July 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: Stakeholders: - (1) PC provider - (2) Social Work (SW) NH champions - (3) post-acute care unit nursing staff and providers (including medical directors) - (4) NH leadership, information technology staff - (5) PLWD and their care partner(s). Person Living with Dementia (PLWD) - documented dementia diagnosis - admitted for post-acute care - age = 60 years - if unable to participate in a conversation or lacking capacity to make healthcare decisions as determined by the NH staff/providers, a care partner who can act as a surrogate decision maker in the PCC-PAC. Exclusion Criteria: Stakeholders: -PLWD who receives the intervention PLWD: - planned discharge within 48 hours of screening - currently receiving hospice care

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Palliative Care Consultation
The PC provider conducts the structured PCC-PAC via videoconference or telephone with the PLWD and/or their care partner and the social work (SW) champion in the NH. The SW and PC provider will set up a mutually agreed upon consultation day/time with the PLWD and/or care partner, within 5 business days of NH admission and follow up visits will occur no more than 30 days later (if needed).

Locations

Country Name City State
United States Collingswood Rehabilitation and Healthcare Center Rockville Maryland

Sponsors (2)

Lead Sponsor Collaborator
University of Maryland, Baltimore National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Primary Outcome Measure Adherence to Skilled Nursing Facility (SNF)-PCC recommendations Adherence Protocol. Medical record review
Investigators will determine a recommendation adherence score after each participants' encounter. Each recommendation will be assigned 2 points, then will define full (2 points), partial (1 point) and no adherence (0 point) to each recommendation. Investigators will sum the points for each SNF-PCC recommendation and use this as the denominator. Investigators will sum each recommendation with full, partial, no adherence and use this as the numerator. The fraction will be converted to a percentage ranging from 0-100% reflecting the recommendation adherence score.
30 days post admission
Secondary Hospitalizations Number of hospitalization(s) 30 days post admission
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