A Phased-Implementation Feasibility and Proof-of-Concept Study to Assess Incorporating the NIDA CTN Common Data Elements (CDEs) Into the Electronic Health Record (EHR) in Large Primary Care Settings ("CDE-EHR-PC" Study), Phase 1
NCT02974335 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 67
Last updated 2022-08-29
Summary
This is a 4-phase study to implement the NIDA CDEs in primary care settings. Collecting and utilizing the CDEs in clinical practice requires a strategy for implementing screening to collect substance use information that populates the CDEs, and assisting primary care providers to offer appropriate interventions by providing clinical decision support (CDS) and a mechanism for making referrals to addiction treatment. We aim to maximize the efficient adoption of screening, CDS, and treatment referrals by integrating all of these activities into the electronic health record (EHR).
The study will be conducted at three sites, representing three large health systems. Each phase will include deliverables essential to move to the next phase, and an independent Advisory Committee will review progress and make recommendations at each transition about how best to progress to each subsequent phase. Based on progress during earlier phases, the Advisory Committee may recommend expansion to additional clinics or health systems during the second part of Phase 4.
Conditions
Interventions
- BEHAVIORAL
-
Interviews with Stakeholders
The information gained from stakeholders will be applied in an iterative process to develop a best-practice approach to screening patients, and to build the EHR tools (CDEs and CDS) that will be further tailored and tested in Phase 2, and then implemented in one clinic in Phase 3.
Sponsors & Collaborators
-
Icahn School of Medicine at Mount Sinai
collaborator OTHER -
Oregon Health and Science University
collaborator OTHER -
Massachusetts General Hospital
collaborator OTHER - lead OTHER
Principal Investigators
-
Jennifer McNeely · New York University Medical School
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-07-25
- Primary Completion
- 2019-04-05
- Completion
- 2019-04-05
Countries
- United States
Study Locations
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