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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05958654
Other study ID # DETECT-RPC
Secondary ID R61AG078523
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 31, 2024
Est. completion date August 31, 2027

Study information

Verified date July 2023
Source The University of Texas Health Science Center, Houston
Contact Michael B Cannell, PhD,MPH
Phone 972-546-2925
Email Michael.B.Cannell@uth.tmc.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate whether the use of the Detection of Elder Mistreatment Through Emergency Care Technicians-Revised for Primary Care (DETECT-RPC) screening tool increases the average reporting of elder mistreatment (EM) by homebased primary care (HBPC) clinicians.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 43
Est. completion date August 31, 2027
Est. primary completion date August 31, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria (physicians): - clinician who actively provides home-based primary care to patients enrolled in one of our partner home-based primary care programs at least part time. Exclusion Criteria: - Inclusion Criteria (patients): - in home-based primary care - 60 years or older - seen by a clinician participating in the study Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Detection of Elder mistreatment Through Emergency Care Technicians-Revised for Primary Care (DETECT-RPC) screening tool
DETECT-RPC is an elder mistreatment (EM) screening tool designed for medics who respond to older adults' homes and will be adapted for home-based primary care (HBPC). The DETECT-RPC tool is designed to (1) be brief, (2) be based on the clinician's direct observations of the older adult and the older adult's physical and social environment, (3) provide reporting guidance, and (4) be integrated into their existing procedures and medical charting software.

Locations

Country Name City State
United States John Hopkins University Medicine International Baltimore Maryland
United States University of Alabama at Birmingham Birmingham Alabama
United States University of Texas Southwestern Medical Center Dallas Texas
United States Baylor College of Medicine Houston Texas
United States The University of Texas health Science Center at Houston( LBJ House Calls Program) Houston Texas
United States The University of Texas Health Science Center at Houston( UT Physicians House Calls Program) Houston Texas
United States University of California San Francisco San Francisco California

Sponsors (2)

Lead Sponsor Collaborator
The University of Texas Health Science Center, Houston National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of reports of EM Data will be collected on the number of reports of EM made by clinicians to the appropriate authorities [for example, adult protective services (APS)] from randomization to termination of data collection (3 years)
Primary Mortality Mortality among patients will be assessed among patients enrolled in the partner home-based primary care programs. from randomization to termination of data collection (3 years)
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