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Opioid Treatment and Recovery Through a Safe Pain Management Program

Primary Purpose

Depression, Opioid Use, Chronic Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Electronic medical recorded clinical decision support [EMR CDS]
Stepped opioid collaborative care model [CCM]
Sponsored by
Ochsner Health System
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Depression

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 18 and older
  2. Have a primary care provider at any of the study clinics
  3. Receiving chronic opioid prescriptions (3 of the prior 4 months) for chronic non-cancer pain
  4. Have a diagnosis of depression or anxiety

Exclusion Criteria:

  1. Age less than 18 years
  2. Active cancer or undergoing cancer treatment
  3. Chronic cancer-related pain
  4. Having a terminal illness
  5. Receiving hospice care

Sites / Locations

  • Ochsner Health System - Research Dept

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Electronic medical recorded clinical decision support

stepped opioid collaborative care model

Arm Description

Usual care only

Usual care AND collaborative care with behavioral health integration

Outcomes

Primary Outcome Measures

Change in rate of high dose opioid prescribing
Change in percent patients with Morphine equivalent daily dose (MEDD) >=50

Secondary Outcome Measures

Change in average daily opioid prescription dosage
Change in the population average MEDD
Change in rate of inpatient hospitalization
Change in rate of inpatient hospitalization visits
Change in rate of emergency department use
Change in rate of emergency department visits
Change in rate of depression symptom response to treatment
Change in Patient Health Questionnaire-9 scores
Change in rate of anxiety symptom response to treatment
Change in Generalized Anxiety Disorder-7 scores
Change in patient rating of Quality of Life
Change in Global Health-10 scores
Change in patient rating of pain control
Change in Pain, Enjoyment, General Activity-3 scores
Change in rate of practice guideline adherence for pain agreements
Change in proportion of patients with pain agreements
Change in rate of practice guideline adherence for urine drug screening
Change in proportion of patients with urine drug screening
Change in rate of practice guideline adherence for naloxone prescriptions
Change in proportion of high risk patients with naloxone prescriptions
Change in rate of patient report of opioid misuse
Change in Current Opioid Misuse Measure-9 scores
Change in rate of referral to specialty care
Change in proportion of patients referred to specialists for pain management
Change in rate of non-opioid prescriptions for pain management
Change in proportion of patients with non-opioid prescriptions for pain management
Change in provider experience with managing mental health conditions
Change in provider ratings of their experience

Full Information

First Posted
March 20, 2019
Last Updated
August 3, 2023
Sponsor
Ochsner Health System
Collaborators
Tulane University School of Public Health and Tropical Medicine, Harvard University
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1. Study Identification

Unique Protocol Identification Number
NCT03889418
Brief Title
Opioid Treatment and Recovery Through a Safe Pain Management Program
Official Title
Opioid Treatment and Recovery Through a Safe Pain Management Program
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
June 30, 2022 (Actual)
Study Completion Date
June 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ochsner Health System
Collaborators
Tulane University School of Public Health and Tropical Medicine, Harvard University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Opioid prescription drug abuse has become a major public health concern in the United States with mortality rates from fatal overdoses reaching epidemic proportions. This opioid crisis coincides with national efforts to improve management of chronic non-cancer pain. The net result, however, has been ever-growing increases in medical expenditures related to prescription costs and increased healthcare service utilization among opioid abusers. Healthcare provider prescribing pattern, especially among non-pain management specialists such as primary care, is a major factor. Louisiana is a major contributor to the epidemic with the 7th highest opioid prescribing rates accompanied by a 12% increase in fatal overdoses. Providers are overdue for implementing safe opioid management strategies in primary care to combat the opioid crisis. Recent practice guidelines provide recommendations on what to do for safe prescribing of opioids, but they do not provide guidance on how to translate them into practice. Health systems must find ways to accelerate guideline adoption in primary care in the face of an overdose crisis. Research that examines a combination workflow- and provider-focused strategies are needed. Given the high prevalence of psychiatric disorders among patients with chronic non-cancer pain, care team expansion with integration of collaborative mental/behavioral health services may be the solution. Collaborative care can extend opioid management beyond standardized monitoring of risk factors for opioid misuse or abuse and set clear protocols for next steps in management. This study is aligned with the National Institute on Drug Abuse's interest in health systems research that examines approaches to screening, assessment, prevention, diagnosis and treatment for prescription drug abuse. It will examine the primary care practice redesign of managing chronic non-cancer pain within a large health system whose 40+ Accountable Care Network-affiliated, adult primary care clinics may serve as an example for transforming opioid management in primary care practices across the country. This four-year type 2 effectiveness-implementation hybrid stepped wedge cluster randomized control trial is designed to compare the clinical and cost effectiveness of electronic medical record-based clinical decision support guided care versus additional integrated, stepped collaborative care for opioid management of primary care patients with chronic non-cancer pain (clinical pharmacist for medication management; licensed clinical social worker for cognitive behavioral therapy and community health worker care coordination); and to examine facilitators and barriers to implementing this multi-component intervention. Investigators anticipate that our study results will elucidate the role of technology versus care team optimization in changing provider opioid prescribing behaviors. Investigators further anticipate that results of our study will demonstrate that integrated mental/behavioral health care for opioid management of chronic non-cancer pain increases value-based care and leads to greater efficiencies in the way that care is delivered.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Opioid Use, Chronic Pain, Anxiety

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
This proposal is a 4-year type 2 effectiveness-implementation hybrid stepped wedge cluster randomized control (cRCT) trial to evaluate a multi-component intervention to: electronic medical recorded (EMR)clinical decision support (CDS) guided care; and stepped opioid collaborative care model (CCM) to improve opioid management of primary care patients with chronic non-cancer pain. The stepped wedge cRCT design will allow us to examine the clinical impact of the intervention as the two components are implemented in a stepwise fashion across the health system. The EMR CDS guided care component went live in all primary care clinics as the health system's standard of practice in October 2017. The stepped opioid CCM component will require 15 months to scale up in 3-month intervals across five geographic regions of the health system in the state of Louisiana. We will randomize the order in which stepped opioid CCM becomes available in each region
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
478 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Electronic medical recorded clinical decision support
Arm Type
Active Comparator
Arm Description
Usual care only
Arm Title
stepped opioid collaborative care model
Arm Type
Active Comparator
Arm Description
Usual care AND collaborative care with behavioral health integration
Intervention Type
Behavioral
Intervention Name(s)
Electronic medical recorded clinical decision support [EMR CDS]
Intervention Description
The opioid management tool has quick links to the Opioid Risk Tool (ORT), health maintenance reminders for risk mitigation tasks (pain management agreements; urine drug screening; prescribing naloxone); Pain Scale and depression/anxiety screen. The frequency with which providers are prompted to complete mitigation tasks is based on patients' level of risk for aberrant drug behavior defined by the ORT score. Additionally, the EMR CDS flags patients as high risk if one of the following criteria are met: (1) co-prescriptions for benzodiazepines; (2) active diagnosis of substance abuse in the last 12 months; or (3) MEDD >=90 mg. The ORT score, morphine equivalent daily dose (MEDD), and hyperlinks to the Louisiana pharmacy drug monitoring program data are visible in the prescription writer. If MEDD >=90 mg, the calculated MEDD is displayed in red font to alert the prescribing provider of high dosage. An Epic banner appears in charts to alert providers of existing pain management agreements.
Intervention Type
Behavioral
Intervention Name(s)
Stepped opioid collaborative care model [CCM]
Intervention Description
The licensed clinical social worker (LCSW) will provide counseling services as indicated (behavioral activation, psychotherapy, crisis planning, facilitating connection to substance abuse counseling and treatment); meet weekly with the consulting psychiatrist for complex case review and care plan adjustments; and supervise the community health worker (CHW) case management and depression/anxiety care management activities. The CHW will update assets and barriers to recovery and self-management and help patients navigate community resources. The clinical pharmacist will review and reconcile active medication lists, assess medication side effects, drug interactions and adverse events; monitor analgesia; recommend algorithm based anti-depression medication titration as indicated. The consulting psychiatrist will directly co-manage patients with severe mental illness, substance abuse and complex medication regimens.
Primary Outcome Measure Information:
Title
Change in rate of high dose opioid prescribing
Description
Change in percent patients with Morphine equivalent daily dose (MEDD) >=50
Time Frame
Baseline, 12-months
Secondary Outcome Measure Information:
Title
Change in average daily opioid prescription dosage
Description
Change in the population average MEDD
Time Frame
Baseline, 12-month
Title
Change in rate of inpatient hospitalization
Description
Change in rate of inpatient hospitalization visits
Time Frame
Baseline, 12-months
Title
Change in rate of emergency department use
Description
Change in rate of emergency department visits
Time Frame
Baseline, 12-months
Title
Change in rate of depression symptom response to treatment
Description
Change in Patient Health Questionnaire-9 scores
Time Frame
Baseline, 12-months
Title
Change in rate of anxiety symptom response to treatment
Description
Change in Generalized Anxiety Disorder-7 scores
Time Frame
Baseline,12-months
Title
Change in patient rating of Quality of Life
Description
Change in Global Health-10 scores
Time Frame
Baseline, 12-months
Title
Change in patient rating of pain control
Description
Change in Pain, Enjoyment, General Activity-3 scores
Time Frame
Baseline, 12-months
Title
Change in rate of practice guideline adherence for pain agreements
Description
Change in proportion of patients with pain agreements
Time Frame
Baseline, 12-months
Title
Change in rate of practice guideline adherence for urine drug screening
Description
Change in proportion of patients with urine drug screening
Time Frame
Baseline, 12-months
Title
Change in rate of practice guideline adherence for naloxone prescriptions
Description
Change in proportion of high risk patients with naloxone prescriptions
Time Frame
Baseline, 12-months
Title
Change in rate of patient report of opioid misuse
Description
Change in Current Opioid Misuse Measure-9 scores
Time Frame
Baseline, 12-months
Title
Change in rate of referral to specialty care
Description
Change in proportion of patients referred to specialists for pain management
Time Frame
Baseline, 12-months
Title
Change in rate of non-opioid prescriptions for pain management
Description
Change in proportion of patients with non-opioid prescriptions for pain management
Time Frame
Baseline, 12-months
Title
Change in provider experience with managing mental health conditions
Description
Change in provider ratings of their experience
Time Frame
Baseline, 12-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 and older Have a primary care provider at any of the study clinics Receiving chronic opioid prescriptions (3 of the prior 4 months) for chronic non-cancer pain Have a diagnosis of depression or anxiety Exclusion Criteria: Age less than 18 years Active cancer or undergoing cancer treatment Chronic cancer-related pain Having a terminal illness Receiving hospice care
Facility Information:
Facility Name
Ochsner Health System - Research Dept
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29559866
Citation
Price-Haywood EG, Robinson W, Harden-Barrios J, Burton J, Burstain T. Intelligent Clinical Decision Support to Improve Safe Opioid Management of Chronic Noncancer Pain in Primary Care. Ochsner J. 2018 Spring;18(1):30-35.
Results Reference
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PubMed Identifier
32113620
Citation
Price-Haywood EG, Burton J, Burstain T, Harden-Barrios J, Lefante J, Shi L, Jamison RN, Bazzano A, Bazzano L. Clinical Effectiveness of Decision Support for Prescribing Opioids for Chronic Noncancer Pain: A Prospective Cohort Study. Value Health. 2020 Feb;23(2):157-163. doi: 10.1016/j.jval.2019.09.2748. Epub 2019 Nov 22.
Results Reference
background
PubMed Identifier
33326877
Citation
Price-Haywood EG, Burton J, Harden-Barrios J, Bazzano A, Lefante J, Shi L, Jamison RN. Depression, anxiety, pain and chronic opioid management in primary care: Type II effectiveness-implementation hybrid stepped wedge cluster randomized trial. Contemp Clin Trials. 2021 Feb;101:106250. doi: 10.1016/j.cct.2020.106250. Epub 2020 Dec 14.
Results Reference
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Opioid Treatment and Recovery Through a Safe Pain Management Program

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