Active — Not RecruitingNot Applicable

The Impact of a Web-Based Naloxone Intervention Under Standing Orders to Patients Prescribed Chronic Opioid Therapy

United States1,004 participantsStarted 2017-12-21

Plain-language summary

In the setting of naloxone standing orders, this study will assess the impact of a targeted, web-based overdose prevention and naloxone intervention for patients prescribed chronic opioid therapy. Outcomes are changes in opioid risk behaviors, naloxone uptake, and knowledge about overdose and naloxone.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18 years of age or greater * Prescribed chronic opioid therapy * Have a health plan which covers the formulation of naloxone available at the pharmacy they received their opioid prescriptions from. Exclusion Criteria: * Non-English speaking, hospice enrollment, do-not-resuscitate order, no internet access

What they're measuring

Change in Opioid-Related Risk Behavior

Timeframe: Change from baseline to 4-6 months, and 8-12 months

Trial details

NCT IDNCT03337009

SponsorKaiser Permanente

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-04-30

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