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Behavioural Intervention

OUD-CDS + Suicide Risk Model associated CDS for Opioid Use Disorder

N/A
Waitlist Available
Led By Rebecca C Rossom, MD, MSCR
Research Sponsored by HealthPartners Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up two time periods: 1) 12 months prior to enrollment (index date), and 2) between enrollment and end of observation period (up to 12 months)
Awards & highlights

Study Summary

This study is evaluating whether a set of activities can help people with opioid use disorder.

Eligible Conditions
  • Opioid Use Disorder
  • Suicide

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~two time periods: 1) 12 months prior to enrollment (index date), and 2) between enrollment and end of observation period (up to 12 months)
This trial's timeline: 3 weeks for screening, Varies for treatment, and two time periods: 1) 12 months prior to enrollment (index date), and 2) between enrollment and end of observation period (up to 12 months) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of Outpatient Visits With Adequate Mental Health Engagement
Number of Participants With CSSRS Completion on the Same Day or in the 14 Days Following Any Outpatient Visit
Number of Participants With One or More Opioid Overdoses
+1 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: OUD-CDS + Suicide Risk Model associated CDS (Intervention arm)Experimental Treatment1 Intervention
Providers that practice in the clinics in this intervention arm will receive access to the OUD-CDS + Suicide Risk Model associated CDS, for all eligible encounters.
Group II: ControlActive Control1 Intervention
Providers that practice in the clinics in this control arm will not receive any access to the OUD-CDS + Suicide Risk Model associated CDS, however these clinical decision-support tools will run "silently" in the background, collecting data on eligible encounters.

Find a Location

Who is running the clinical trial?

HealthPartners InstituteLead Sponsor
184 Previous Clinical Trials
3,716,044 Total Patients Enrolled
National Institute on Drug Abuse (NIDA)NIH
2,461 Previous Clinical Trials
2,616,888 Total Patients Enrolled
Hennepin Healthcare Research InstituteOTHER
90 Previous Clinical Trials
77,062 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~31 spots leftby Apr 2025