Mode
Text Size
Log in / Sign up
N/A N=53,132

Physician Coaching to Reduce Opioid-related Harms

Substance Abuse · Chronic Pain

Enrolled (actual)
53,132
Serious AEs
0.0%
Results posted
Jul 2018
Primary outcome: Primary: Overall Rate of Opioid Prescribing — 0.012; 0.013 Proportion of patients

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Physician coaching (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Wisconsin, Madison
Primary completion
Jun 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Rate of Opioid Prescribing
0.012; 0.013
SECONDARY
Rate of Opioid / Benzodiazepine Co-prescribing
0.074; 0.061
SECONDARY
Urine Drug Screening Rate
0.645; 0.440
SECONDARY
Mental Health Screening Rate
0.574; 0.394
SECONDARY
Use of Pain Management Agreements
0.782; 0.542
SECONDARY
High-dose Patients
0.191; 0.125
SECONDARY
Provider Drop-out Rate
0; 0
SECONDARY
Participating Patient Demographics
47.1; 49.7; 2.2; 2.5; 2.4; 1.6
SECONDARY
Participating Clinic Characteristics
29956; 13296; 9813; 34; 13; 20
SECONDARY
Participating Staff Characteristics
6; 1; 4; 3; 1; 2
SECONDARY
Intervention Fidelity
237.7; 85.7
SECONDARY
Intervention Cost
29379
SECONDARY
Proportion With MEDD >120 mg
0.191; 0.125
SECONDARY
Average Morphine Equivalent Daily Dose (MEDD)
84.3; 60.2

Summary

This project pilot tests an innovative clinical guideline translation and physician coaching model to promote adherence to evidence-based guidelines for the prescribing of opioid pain medications in primary care settings.

Eligibility Criteria

Inclusion Criteria

At each of the 4 coaching intervention sites, we aim to recruit between 3-7 clinical care providers with prescribing authority (e.g., primary care physicians, mid-level practitioners, etc.) to participate in interviews and focus groups. All clinic staff (e.g., medical assistants, office staff) are welcome to participate in coaching site visits and follow up correspondence, but only staff with prescribing authority will be considered research participants.

Exclusion Criteria

  • Residents will be excluded.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02433496). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search