Skip to main content
Clinical Trials/NCT02861976
NCT02861976CompletedNot Applicable

Screening in Trauma for Opioid Misuse Prevention (STOMP): Screen Development and Pilot Implementation Study

University of Wisconsin, Madison1 site in 1 country346 target enrollmentStarted: July 15, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
346
Locations
1
Primary Endpoint
Opioid use disorder (CIDI-SAM) or opioid misuse (COMM) Opioid Use Disorder in 6 Months Post Traumatic Injury

Study Overview

Brief Summary

The current study seeks to begin the crucial work of creating effective protocols to prevent opioid misuse, addiction, and related complications by developing and pilot testing an opioid risk screening protocol at Wisconsin trauma centers.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Inpatient victim of traumatic injury
  • Expected need for post-discharge outpatient opioid analgesia
  • English speaking
  • Disposition to short-term rehabilitation facility is allowed

Exclusion Criteria

  • Disposition to a skilled nursing or long-term acute care facility
  • Current active opioid use disorder or current active participation in a program of recovery for another substance use disorder

Outcomes

Primary Outcomes

Opioid use disorder (CIDI-SAM) or opioid misuse (COMM) Opioid Use Disorder in 6 Months Post Traumatic Injury

Time Frame: 6 months subject participation

This data will be analyzed in tandem with patient demographics, physical and mental health, and hypothesized risk factors for opioid misuse.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials