Consensus-based Algorithms to Address Opioid Misuse Behaviors Among Individuals Prescribed LTOT
Primary Purpose
Opioid Misuse, Chronic Pain
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pilot study of algorithms implementation package
Sponsored by
About this trial
This is an interventional health services research trial for Opioid Misuse focused on measuring Long-Term Opioid Therapy, Algorithms, Opioid Misuse, Chronic Pain
Eligibility Criteria
Inclusion Criteria:
- UPMC community primary care practices
Exclusion Criteria:
- non-UPMC practices
Sites / Locations
- University of Pittsburgh
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Implementation bundle
Arm Description
Participating clinics will experience integration of the "Implementation Bundle" into their practices.
Outcomes
Primary Outcome Measures
Feasibility of algorithms
Number of algorithms used by Primary Care Physicians (PCPs) during the study period, measured by surveys administered to the PCPs at the end of the study period.
Acceptability of algorithms
Level of acceptability of the algorithms will be measured via qualitative interviews with clinicians and staff at each of the clinics.
Secondary Outcome Measures
Preliminary Effectiveness of algorithms
Change in opioid misuse behaviors as assessed using the Electronic Health Record and natural language processing methods.
Full Information
NCT ID
NCT05182606
First Posted
November 28, 2021
Last Updated
October 3, 2023
Sponsor
University of Pittsburgh
Collaborators
National Institute on Drug Abuse (NIDA)
1. Study Identification
Unique Protocol Identification Number
NCT05182606
Brief Title
Consensus-based Algorithms to Address Opioid Misuse Behaviors Among Individuals Prescribed LTOT
Official Title
Consensus-based Algorithms to Address Opioid Misuse Behaviors Among Individuals Prescribed Long-term Opioid Therapy: Developing Implementation Strategies and Pilot Testing
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 1, 2022 (Actual)
Primary Completion Date
September 30, 2023 (Actual)
Study Completion Date
September 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
National Institute on Drug Abuse (NIDA)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The NIH Helping to End Addiction Long-term (HEAL) initiative has identified a critical next step to addressing the opioid crisis: improving treatments for opioid misuse behaviors (e.g., using more opioids than prescribed, illicit substance use) in patients prescribed long-term opioid therapy for chronic pain. In previous work, the investigators have developed innovative consensus-based algorithms to manage these behaviors. By developing implementation strategies for these algorithms, this project is directly responsive to the HEAL initiative and promises to reduce opioid misuse-related harms.
Detailed Description
Despite a growing understanding of the risks of long-term opioid therapy (LTOT), it continues to be frequently prescribed and remains a mainstay of treatment for chronic pain. The Centers for Disease and Control (CDC) Guideline for Prescribing Opioids for Chronic Pain is geared toward primary care providers and has been adopted as the standard of care by many healthcare organizations and insurers. Importantly, it encourages monitoring of patients on LTOT for opioid-related harms. By implementing monitoring, primary care providers may uncover various concerning behaviors, sometimes called aberrant drug-related behaviors or opioid misuse behaviors, that arise among individuals prescribed LTOT for chronic pain. These behaviors (e.g., missed appointments, using more opioid medication than prescribed, asking for an increase in opioid dose, aggressive behavior, and alcohol and other substance use) are common, concerning, and may represent unsafe use of LTOT or a developing opioid use disorder (OUD). However, the CDC Guideline and other existing evidence do not provide specific, detailed guidance about how to address concerning behaviors when they occur. Therefore, there is a critical need to understand how to best respond to these behaviors. The long-term goal of our program of research is to reduce LTOT-related harms, particularly from opioid misuse, and diminish their impact on the U.S. opioid epidemic. As a first step toward accomplishing this goal, the investigators conducted a Delphi study to rigorously establish consensus-based approaches to managing common and challenging concerning behaviors, from which algorithms were created. Identifying and operationalizing implementation strategies using an evidence-based framework are the critical next steps that must occur before any testing of the algorithms.
The investigators successfully uncovered optimal implementation strategies through primary care provider experiences with Standardized Patients (SPs) followed by CFIR- and ERIC-guided individual interviews. Using our prior expertise developing clinic-wide opioid risk reduction strategies and a Patient-Provider advisory board, the investigators developed a comprehensive "implementation package" that can be delivered to primary care practices.
The investigators now aim to conduct a pilot trial to test the algorithm implementation package. Guided by the CFIR-based implementation plan and using the implementation package that the investigators developed, pilot trial will be conducted to investigate feasibility, acceptability, and preliminary effectiveness of the algorithm implementation package.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Misuse, Chronic Pain
Keywords
Long-Term Opioid Therapy, Algorithms, Opioid Misuse, Chronic Pain
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Investigators will conduct a pilot trial to investigate the feasibility, acceptability, and preliminary effectiveness of the algorithm Implementation Package. The investigators will conduct the pilot in 3 University of Pittsburgh Medical Center (UPMC) practices. the investigators will randomize by site and use a waitlist control. Feasibility and acceptability will be assessed qualitatively and via a clinician survey. Preliminary effectiveness outcomes will include reduction in concerning behaviors and increased diagnosis/treatment of Opioid Use Disorder (OUD). The investigators will also pilot Electronic Health Record-based outcomes assessment.
Masking
None (Open Label)
Allocation
N/A
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Implementation bundle
Arm Type
Experimental
Arm Description
Participating clinics will experience integration of the "Implementation Bundle" into their practices.
Intervention Type
Behavioral
Intervention Name(s)
Pilot study of algorithms implementation package
Intervention Description
The "Implementation Bundle" will include a link to algorithms in the Electronic Health Record, Smartphrases, audited feedback, and instructions.
Primary Outcome Measure Information:
Title
Feasibility of algorithms
Description
Number of algorithms used by Primary Care Physicians (PCPs) during the study period, measured by surveys administered to the PCPs at the end of the study period.
Time Frame
1 year
Title
Acceptability of algorithms
Description
Level of acceptability of the algorithms will be measured via qualitative interviews with clinicians and staff at each of the clinics.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Preliminary Effectiveness of algorithms
Description
Change in opioid misuse behaviors as assessed using the Electronic Health Record and natural language processing methods.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
UPMC community primary care practices
Exclusion Criteria:
non-UPMC practices
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jessica Merlin
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15231
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Consensus-based Algorithms to Address Opioid Misuse Behaviors Among Individuals Prescribed LTOT
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