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Patient Reported Outcomes for Opioid Use Disorder

NCT03985163 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2024-02-16

No results posted yet for this study

Summary

The goal of the project is to build a clinical data research infrastructure that will begin to enhance capacity to use electronic health record (EHR) data and patient reported outcomes measures (PROs) to conduct opioid related research in emergency departments (EDs). 200 adult patients with a history of non-medical opioid use, opioid use disorder, or acute opioid overdose will be enrolled and will be asked to complete three PRO surveys (baseline, 3 days post ED discharge, and 30 days post discharge).

Conditions

  • Opioid-use Disorder
  • Overdose of Opiate
  • Patient Participation

Interventions

OTHER

Patient Reported Outcomes Electronic Survey

This study does not include a drug, test, behavioral or medical procedure intervention; participants will be asked to complete three surveys

Sponsors & Collaborators

  • National Drug Abuse Treatment Clinical Trials Network

    collaborator NETWORK

  • National Institute on Drug Abuse (NIDA)

    collaborator NIH

  • Yale University

    lead OTHER

Principal Investigators

  • Kathryn Hawk, MD · Yale University School of Medicine Department of Emergency Medicine

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-06-07
Primary Completion
2020-02-16
Completion
2020-02-16

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03985163 on ClinicalTrials.gov