ACTIVE_NOT_RECRUITING

Developing a Tailored Stigma Reduction Intervention to Increase Buprenorphine Prescribing

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Buprenorphine is an evidence-based treatment for opioid use disorder that also has strong potential to reduce HIV transmission in people who use drugs. Rural health care professionals are eligible and critically needed to provide these medications, but stigma currently limits provider willingness to prescribe buprenorphine, especially in regions where mortality and HIV transmission secondary to opioid use are high. In this developmental trial, the investigators will adapt, refine, and test the feasibility of a prototype brief stigma-reduction training intervention aimed at increasing buprenorphine prescribing in the rural primary care setting.

Official Title

Developing a Tailored Stigma Reduction Intervention to Increase Buprenorphine Prescribing Among Rural Primary Care Providers in Ohio

Quick Facts

Study Start:2022-09-01
Study Completion:2025-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05505227

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * physician, nurse practitioner, or physician assistant
  2. * eligible to prescribe buprenorphine under federal law
  3. * currently practices in primary care setting
  4. * currently practices in rural-designated county
  5. * at least 18 years of age
  1. * currently prescribing buprenorphine at full capacity

Contacts and Locations

Principal Investigator

Berkeley Franz, Ph.D.
PRINCIPAL_INVESTIGATOR
Ohio University Heritage College of Osteopathic Medicine

Study Locations (Sites)

Berkeley Franz
Athens, Ohio, 45701
United States

Collaborators and Investigators

Sponsor: Ohio University

  • Berkeley Franz, Ph.D., PRINCIPAL_INVESTIGATOR, Ohio University Heritage College of Osteopathic Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-09-01
Study Completion Date2025-06-30

Study Record Updates

Study Start Date2022-09-01
Study Completion Date2025-06-30

Terms related to this study

Additional Relevant MeSH Terms

  • Opioid-Related Disorders
  • Buprenorphine
  • Social Stigma
  • Rural Health Services