- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05958654
DETECT-RPC Universal EM Screening (DETECT-RPC)
Detection of Elder Mistreatment Through Emergency Care Technicians - Revised for Primary Care (DETECT-RPC) Universal EM Screening
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Michael B Cannell, PhD,MPH
- Phone Number: 972-546-2925
- Email: Michael.B.Cannell@uth.tmc.edu
Study Contact Backup
- Name: James S Barnes
- Phone Number: 972-546-2934
- Email: James.S.Barnes@uth.tmc.edu
Study Locations
-
-
Alabama
-
Birmingham, Alabama, United States, 35294
- Recruiting
- University of Alabama at Birmingham
-
Contact:
- Marianthe Grammas, MD
- Phone Number: 205-996-2770
- Email: mdgrammas@uabmc.edu
-
-
California
-
San Francisco, California, United States, 94143
- Recruiting
- University of California San Francisco
-
Contact:
- Maria Yefimova, PhD, RN
- Phone Number: 415-203-4947
- Email: maria.yefimova@usf.edu
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-
Maryland
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Baltimore, Maryland, United States, 21218
- Recruiting
- John Hopkins University Medicine International
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Contact:
- Thomas Dr. Cudjoe, MD. MPH, MA
- Phone Number: 443-927-1638
- Email: tcudjoe2@jhmi.edu
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-
Texas
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Dallas, Texas, United States, 75390
- Recruiting
- University of Texas Southwestern Medical Center
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Contact:
- Debbie Freeland, MD
- Email: Deborah.Freeland@UTSouthwestern.edu
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Houston, Texas, United States, 77030
- Recruiting
- Baylor College of Medicine
-
Contact:
- Kristina Little, MD
- Phone Number: 713-814-4505
- Email: Kristina.Little@bcm.edu
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Houston, Texas, United States, 77030
- Recruiting
- The University of Texas health Science Center at Houston( LBJ House Calls Program)
-
Contact:
- Julia Hiner, MD
- Phone Number: 713-500-6283
- Email: Julia.A.Hiner@uth.tmc.edu
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Houston, Texas, United States, 77030
- Recruiting
- The University of Texas Health Science Center at Houston( UT Physicians House Calls Program)
-
Contact:
- Faith B Atai, MD
- Phone Number: 713-500-6628
- Email: Faith.D.Atai@uth.tmc.edu
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria (Clinicians):
- Clinician who actively provides home-based primary care (HBPC) to patients enrolled in one of our partner home-based primary care programs at least part time.
Exclusion Criteria (Clinicians):
- HBPC Clinicians must be a physician, nurse practitioner, or physician assistant who actively provides home-based primary care to patients enrolled at a partner site HBPC at least part time
Inclusion Criteria (patients):
- in home-based primary care
- 60 years or older
- seen by a clinician participating in the study
Exclusion Criteria (patients)
- Must be aged 60 and older, enrolled in a site-specific partner HBPC and treated in their primary residence
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: with DETECT-RPC screening tool
|
DETECT is an elder mistreatment (EM) screening tool created for medics in the Fort Worth Texas area to use when responding to the homes of older adults, enabling them to screen for signs of elder mistreatment. DETECT-RPC is the adapted version of this tool designed specifically for use by home-based primary care (HBPC) clinicians. The DETECT-RPC tool is designed to:
Other Names:
|
|
No Intervention: without DETECT-RPC screening tool
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
number of reports of EM
Time Frame: from randomization to termination of data collection (3 years)
|
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)
|
|
Mortality
Time Frame: from randomization to termination of data collection (3 years)
|
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)
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Michael B Cannell, PhD,MPH, The University of Texas Health Science Center, Houston
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- DETECT-RPC
- 4R33AG078523-03 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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