Status:
COMPLETED
Evaluation of an Interactive Opioid Risk Education Program (STOMP) for Parents
Lead Sponsor:
University of Michigan
Collaborating Sponsors:
National Institute on Drug Abuse (NIDA)
Conditions:
Pain, Postoperative
Medication Adherence
Eligibility:
All Genders
21-99 years
Phase:
NA
Brief Summary
Millions of children and adolescents are prescribed opioid pain relievers each year, placing them at risk for serious adverse events and misuse in the home setting. Parents who manage these medicines,...
Detailed Description
The overarching goal of this research is to improve opioid analgesic safety and efficacy by optimizing opioid risk recognition, informed analgesic decision-making, and drug storage/disposal behaviors ...
Eligibility Criteria
Inclusion
- Parent (\>=21yr) and child (5-17 yr) (dyad) who lives in the home and is prescribed an opioid for postoperative pain management
- English speaking
Exclusion
- Child is undergoing a non-elective procedure
- Child cannot self-report pain levels (i.e., is cognitively impaired)
- Child has a hematologic/oncologic condition
- Child has a kidney or liver conditions that precludes the usual analgesic prescription pattern (opioid plus a non-opioid)
- Child has been taking opioids for prolonged pain pre-operatively (\>2 weeks)
Key Trial Info
Start Date :
October 24 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 30 2019
Estimated Enrollment :
712 Patients enrolled
Trial Details
Trial ID
NCT03287622
Start Date
October 24 2017
End Date
September 30 2019
Last Update
November 19 2020
Active Locations (1)
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1
University of Michigan, C.S. Mott Children's Hospital
Ann Arbor, Michigan, United States, 48109