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Validation of a Community Pharmacy-Based Prescription Drug Monitoring Program Risk Screening Tool

Validation of a Community Pharmacy-Based Prescription Drug Monitoring Program Risk Screening Tool

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03936985
Acronym
PHARMSCREEN
Enrollment
1464
Registered
2019-05-03
Start date
2019-11-04
Completion date
2023-05-31
Last updated
2024-07-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Abuse, Prescription Drug Abuse (Not Dependent)

Brief summary

The goal of the study is to validate a Prescription Drug Monitoring Program-based opioid risk metric to discriminate between low, moderate, and high-risk opioid use disorder. The World Health Organization Alcohol, Smoking, and Substance Involvement Screening Test (WHO ASSIST) will be used as the gold standard instrument that defines patient risk levels. No intervention or hypothesis will be tested.

Detailed description

Fatal overdose deaths involving prescription opioids, heroin, and synthetic opioids has continued to increase across the US-continuing to increase in 35 states from 2013-2017. Given these persistent trends for adverse opioid-related outcomes in populations across the US, it is critical to work to identify those who are at risk, deliver appropriate care that will help prevent progression to more severe opioid-related outcomes, and provide referral and treatment resources to those who suffer from opioid use disorder. Therefore, it is necessary to expand the continuum of care to health care settings that previously may have been underutilized. One underutilized resource for addressing the current opioid epidemic is community pharmacies.The most important clinical tool pharmacists have available to identify possible misuse of opioid medications is prescription drug monitoring programs (PDMP),which capture patient-level prescription dispensing information to inform monitoring, dispensing decisions, and possible intervention.These tools are available in all US states and have the potential to enable pharmacists to identify patients at-risk for opioid-related adverse events, such as addiction and overdose. In light of the continued escalation of the opioid epidemic nationally, combined with the promising opportunities afforded by the further inclusion of community pharmacy settings for engaging patients with opioid-related risk, it is important to evaluate whether current PDMP risk metrics correlate with clinically validated opioid risk tools and if clinically meaningful risk cutoffs exist for PDMP risk metrics. This study will evaluate the concurrent validity of a PDMP-based opioid risk metric as a clinical measure of high risk opioid use and establish clinically useful risk-level thresholds relative to the widely validated gold standard of the World Health Organization Alcohol, Smoking, and Substance Involvement Screening Test (WHO ASSIST). This study is a one group, cross-sectional, health assessment study. Participants who enroll in the study will complete on-line surveys at a single time point. Approximately 1,523 patients will be recruited from approximately 15 community community pharmacies. Trained pharmacy staff will inform potentially eligible participants, or individuals receiving at least one prescription(s) for potentially eligible participants, of the survey opportunity. Patients recruited will complete validated measures to assess opioid use and risk behaviors, substance use, and physical and mental health. A series of a priori analyses will be conducted to evaluate the validity of the PDMP-based opioid risk metric relative to the widely validated gold standard WHO ASSIST and to identify cutoff thresholds. Correlational, regression, and Cohen's Kappa statistical analyses will also be conducted to evaluate the relationship between the risk metric and the WHO ASSIST.

Interventions

None listed

Sponsors

University of Cincinnati
CollaboratorOTHER
Purdue University
CollaboratorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Utah
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. be dispensed ≥1 opioid medication (including tramadol) by a participating pharmacy; 2. be ≥18 years of age according to pharmacy data and self-report

Exclusion criteria

1. solely filling buprenorphine or buprenorphine combination products i.e., patients receiving OUD treatment with no other opioid medication use; 2. currently receiving treatment for cancer; 3. having previously completed the survey; 4. having current involvement with the criminal justice system that has, or could, lead to incarceration

Design outcomes

Primary

MeasureTime frameDescription
Validity of the PDMP Narcotic Score Versus the WHO ASSISTThe ASSIST was administered once at Day 1.To assess the validity of the PDMP Narcotic Score, the AUC (Area Under the Curve) was used. AUC ranges in value from 0 to 1. A model whose predictions are 100% wrong has an AUC of 0.0; one whose predictions are 100% correct has an AUC of 1.0. And when AUC is 0.5, it means the model has no means of separating between the different groups. For this study, the closer to 1.0 the more similar the PDMP Narcotic Score is to the WHO ASSIST.

Countries

United States

Participant flow

Participants by arm

ArmCount
All Participants
Study participants were patients of one of the 19 study pharmacies, completed the survey, and had sufficient data in the prescription drug monitoring program to generate the Narcotic Score (NS)
1,464
Total1,464

Baseline characteristics

CharacteristicAll Participants
Age, Continuous49.6 years
STANDARD_DEVIATION 14.8
Ethnicity (NIH/OMB)
Hispanic or Latino
17 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
1447 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Prescription Opioids
High
33 Participants
Prescription Opioids
Low
772 Participants
Prescription Opioids
Moderate
623 Participants
Prescription Opioids
Unknown/Not responded
36 Participants
Sex: Female, Male
Female
911 Participants
Sex: Female, Male
Male
553 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 0
other
Total, other adverse events
0 / 0
serious
Total, serious adverse events
0 / 0

Outcome results

Primary

Validity of the PDMP Narcotic Score Versus the WHO ASSIST

To assess the validity of the PDMP Narcotic Score, the AUC (Area Under the Curve) was used. AUC ranges in value from 0 to 1. A model whose predictions are 100% wrong has an AUC of 0.0; one whose predictions are 100% correct has an AUC of 1.0. And when AUC is 0.5, it means the model has no means of separating between the different groups. For this study, the closer to 1.0 the more similar the PDMP Narcotic Score is to the WHO ASSIST.

Time frame: The ASSIST was administered once at Day 1.

Population: Participants who complete the World Health Organization Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST).

ArmMeasureValue (NUMBER)
High to Moderate RiskValidity of the PDMP Narcotic Score Versus the WHO ASSIST.70 probability
Moderate to Low RiskValidity of the PDMP Narcotic Score Versus the WHO ASSIST.74 probability

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026