Clinical Decision Support for Opioid Use Disorders in Medical Settings: Usability Testing in an EMR
NCT ID: NCT03559179
Last Updated: 2020-03-17
Study Results
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View full resultsBasic Information
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COMPLETED
NA
55 participants
INTERVENTIONAL
2018-04-30
2019-02-14
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Waivered Providers Receive the Opioid Wizard
All providers who have a buprenorphine waiver will receive the OUD clinical decision support tool (Opioid Wizard).
Opioid Wizard
The Opioid Wizard is an OUD clinical decision support tool for primary care providers.
Does not Receive the Opioid Wizard
All non-buprenorphine waivered providers will be randomized to receive or not receive the Opioid Wizard. This arm of providers will continue to treat their patients as usual.
No interventions assigned to this group
Non-Waivered Providers who receive Opioid Wizard
All non-buprenorphine waivered providers will be randomized to receive or not receive the Opioid. This arm of providers will receive the OUD clinical decision support tool (Opioid Wizard).
Opioid Wizard
The Opioid Wizard is an OUD clinical decision support tool for primary care providers.
Interventions
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Opioid Wizard
The Opioid Wizard is an OUD clinical decision support tool for primary care providers.
Eligibility Criteria
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Inclusion Criteria
* Have at least schedule 3 DEA prescribing privileges
* Voluntarily provide written informed consent to participate in this study
Exclusion Criteria
ALL
Yes
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
Hennepin Healthcare Research Institute
OTHER
HealthPartners Institute
OTHER
Responsible Party
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Locations
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HealthPartners
Bloomington, Minnesota, United States
Countries
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References
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Rossom RC, Sperl-Hillen JM, O'Connor PJ, Crain AL, Nightingale L, Pylkas A, Huntley KV, Bart G. A pilot study of the functionality and clinician acceptance of a clinical decision support tool to improve primary care of opioid use disorder. Addict Sci Clin Pract. 2021 Jun 15;16(1):37. doi: 10.1186/s13722-021-00245-7.
Provided Documents
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Document Type: Study Protocol
Document Type: Statistical Analysis Plan
Document Type: Informed Consent Form
Other Identifiers
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0076-ot
Identifier Type: -
Identifier Source: org_study_id
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