N/A
N=4,939
Improving Health and Employment Outcomes Through Workplace Opioid Policies
Opioid-Related Disorders
Bottom Line
View on ClinicalTrials.gov: NCT05387408 ↗Enrolled (actual)
4,939
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcome: Primary: Proportion of Workers With Opioid Misuse, Opioid Use Disorder and Opioid Overdose: Administrative Data [Primary Outcome]
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Best Practice Health and Employment Opioid-related Policies (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Washington University School of Medicine
- Primary completion
- Mar 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Proportion of Workers With Opioid Misuse, Opioid Use Disorder and Opioid Overdose: Administrative Data [Primary Outcome] |
— | — |
| PRIMARY Proportion of Workers With Opioid Misuse: Worker Surveys |
— | — |
| SECONDARY Proportion of Workers With Lost Time: Worker Surveys [Secondary Outcome] |
— | — |
| SECONDARY Proportion of Workers Who Are Willing to Seek Help: Worker Surveys [Secondary Outcome] |
— | — |
Summary
Evaluate the feasibility of implementing workplace opioid guidelines in the construction trades; define and collect measures of implementation and efficacy. The investigators will implement the intervention in three local union health funds, evaluate the implementation using the Reach, Effectiveness, Adoption, Implementation, Maintenance (RE-AIM) framework, and collect the data needed to measure the efficacy of health changes due to implementation of the intervention (workplace opioid guidelines). This is only a feasibility trial in preparation for conducting an randomized control trial. For the efficacy trial, the investigators will measure pre-post health change using two data sources: 1) administrative health claims and electronic member work hours, and 2) worker/member surveys. To monitor implementation of the intervention, the investigators will measure changes made to the health funds opioid prevention program through qualitative interviews with the health fund manager and through worker surveys for worker awareness and use of the health fund program changes pre-post implementation. The efficacy outcomes for the administrative health (and pharmacy) claims and work hours record will measure opioid prescriptions, chronic opioid use, and OUD in health claims and pharmacy data (details below). The efficacy outcomes for the worker surveys will record changes in misuse of opioids, change in missed days/work productivity, change in attitudes toward seeking help if worker was struggling with opioid misuse, and awareness and use of health fund programs (i.e. employee assistance programs, healthcare recovery services). the investigators will collect data at baseline and and after 6 months for the study of implementation and efficacy (a pre/post design, one-arm trial).
Eligibility Criteria
Inclusion Criteria
- members enrolled in union health funds
Exclusion Criteria
- none.
Data sourced from ClinicalTrials.gov (NCT05387408). 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.