Targeting Effective Analgesia in Clinics for HIV - Intervention
NCT02564341 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 41
Last updated 2018-11-20
Summary
The TEACH randomized controlled trial will test the effectiveness of a collaborative care intervention directed towards physicians who provide care for HIV-infected persons to improve the quality of care for prescribing chronic opioid therapy (COT) for pain and reduce the misuse of prescription opioids among HIV-infected persons.
Conditions
- HIV Infection
- Pain
- Drug Dependence
Interventions
- BEHAVIORAL
-
Collaboration with an IT enabled nurse care manager
The nurse care manager at each site will collaborate with intervention physicians to implement key essential elements of guideline driven care, namely opioid treatment agreements, urine drug testing, random pill counts and periodic checking of on-line Prescription Monitoring Programs. The nurse care manager will use an electronic registry to retrieve pain medication information from the electronic medical record (EMR). Registry data will be collected on the patients of the intervention group providers. The nurse care manager will be able to use the registry to generate reports that will allow him/her to monitor those patients who are receiving opioids for chronic pain.
- BEHAVIORAL
-
Education and academic detailing
All intervention participants will receive a 60 minute group didactic session by a national expert on opioid prescribing for pain. Physicians will receive two academic detailing sessions, and will be given the option of having a third, booster academic detailing session if desired.
- BEHAVIORAL
-
Facilitated access to a specialist in addictions
The nurse care manager will encourage and arrange referral of challenging patients with potential abuse or dependence to prescription opioids to an addiction specialist.
Sponsors & Collaborators
-
National Institute on Drug Abuse (NIDA)
collaborator NIH -
Emory University
collaborator OTHER -
Grady Health System
collaborator OTHER -
Boston Medical Center
lead OTHER
Principal Investigators
-
Jeffrey Samet, MD, MA, MPH · Boston Medical Center
-
Carlos del Rio, MD · Emory University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-09-30
- Primary Completion
- 2018-11-30
- Completion
- 2018-11-30
Countries
- United States
Study Locations
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