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The Emergency Department Longitudinal Integrated Care (ED-LINC2)

Primary Purpose

Opioid Use Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ED-LINC
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Opioid Use Disorder focused on measuring collaborative care, opioid use disorder (OUD), substance use disorder

Eligibility Criteria

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

Inclusion Criteria:

  • Aged 18 years or older
  • Moderate or Severe OUD based on the Structured Clinical Interview for DSM Disorders (SCID)
  • Currently have a phone or method of contact
  • Able to provide a phone number and one additional piece of contact information

Exclusion Criteria:

  • Incarcerated or under arrest
  • Non-English speaking
  • Live beyond a 50 mile radius of Harborview Medical Center
  • Require active resuscitation in the ED or other clinical area at the time of Research Assistant (RA) approach
  • Are receiving palliative care services or hospice care for a chronic illness such as metastatic cancer
  • Are in the ED or hospital for a primary psychiatric emergency such as suicidal ideation or attempt and require emergent evaluation by a Psychiatrist
  • Receiving chronic opioid therapy (COT) defined as prescription opioids for most days out of the last 90 days for a chronic pain condition
  • In the ED for sexual assault
  • Enrolled or eligible for state-funded or hospital-funded care coordination program based on high utilization of the ED

Sites / Locations

  • Harborview Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Usual Care

ED-LINC Intervention

Arm Description

Participants assigned to this arm will receive usual care.

Patients assigned to the ED-LINC intervention will receive 1) overdose education, 2) brief bedside intervention targeting motivation to engage in outpatient care, 3) a patient-centered approach to MOUD using a treatment decision support tool, 4) longitudinal and proactive care management and 5) weekly caseload supervision allowing for stepped-up care targeting opioid use and comorbidity.

Outcomes

Primary Outcome Measures

Change in Illicit Opioid Use Over Time
To compare self-reported past-30 day illicit opioid use using the validated self-report measure of timeline followback (TLFB) in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit.
Initiation of Medications for OUD
To compare the frequency of initiation of medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD at scheduled follow-up intervals.
Change in Emergency Department visits
To compare changes over time in Emergency Department visits in subjects receiving usual care or ED-LINC intervention; Emergency Department visits will be measured by the Emergency Department Information Exchange (an automated health information exchange) that caputures population-level Emergency Department utilization for all enrolled participants.

Secondary Outcome Measures

Intervention effect when associated with Methamphetamine use
Explore the impact of methamphetamine use, as measured by the timeline follow-back (TLFB) which is a validated patient self-report measure of days of methamphetamine use over a 30 day-period, on intervention treatment effects.
Time to Initiation of MOUD
To compare time to initiation of medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit.
Engagement in Medications for OUD
To compare the frequency of engagement in medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC over the course of the year after the index Emergency Department visit using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD at scheduled follow-up intervals.
Retention in Medications for OUD
To compare the frequency of retention in medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit visit using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD at scheduled follow-up intervals.
Intervention effect when associated depression
Explore the impact of depression in the past 30-days as measured by self-report PHQ-9 at baseline on intervention treatment effects.
Intervention effect when associated anxiety
Explore the impact of anxiety in the past 30-days as measured by self-report GAD-7 at baseline on intervention treatment effects.
Intervention effect when associated PTSD
Explore the impact of PTSD in the past 30-days as measured by self-report PCL-C at baseline on intervention treatment effects.baseline on intervention treatment effects.
Intervention effect when associated current pain
Explore the impact of pain in the past week as measured by the self-report 3-item PEG at baseline on intervention treatment effects.
Intervention effect when patient has exposure to MOUD in prior 12 months
Explore the impact of any past 12-month MOUD exposure prior to enrollment where MOUD includes buprenorphine, methadone and/or naltexone assessed from review of medical records, using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD obtained at baseline on the intervention treatment effect.
Intervention effect by sex
Explore the impact of patient sex as measured by patient self-report at baseline on intervention treatment effects
Intervention effect when patient reports using illicit fentanyl at baseline
Explore the impact of fentanyl use as measured by any patient self-report fentanyl use in the past 30-days at baseline on the intervention treatment effect

Full Information

First Posted
February 18, 2022
Last Updated
May 13, 2022
Sponsor
University of Washington
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT05327166
Brief Title
The Emergency Department Longitudinal Integrated Care
Acronym
ED-LINC2
Official Title
The Emergency Department Longitudinal Integrated Care Effectiveness Randomized Trial Targeting Opioid Use and Related Comorbidity From the ED
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 12, 2022 (Actual)
Primary Completion Date
April 30, 2026 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Collaborative care is a comprehensive patient-centered model of healthcare delivery targeting behavioral health or substance use that stems from the chronic disease management framework. The intervention being tested ('Emergency Department Longitudinal Integrated Care' or ED LINC) derives from the collaborative care model and has demonstrated feasibility in previous studies. This study expands on the model to test the effectiveness of the ED-LINC intervention when compared with usual care. The study team primarily hypothesizes that patients randomized to the ED-LINC intervention, when compared to patients randomized to usual care, will demonstrate: 1) significant reductions in self-report illicit opioid use, 2) significant increases in initiation and retention of medications for opioid use disorder, and 3) significant reductions in ED utilization.
Detailed Description
This is a randomized clinical trial designed to test the effectiveness of the multi-component ED-LINC intervention. Patients with moderate or severe OUD seeking medical care at 2 EDs in Seattle, Washington, who provide informed consent will be randomized to the ED-LINC intervention (n=250) or usual care control (n=250) conditions. ED-LINC will include: 1) overdose education, 2) brief bedside intervention targeting motivation to engage in outpatient care, 3) a patient-centered approach to medications for opioid use disorder (MOUD) using a treatment decision support tool, 4) longitudinal and proactive care management which will proceed for approximately 3 months, and 5) weekly caseload supervision allowing for stepped-up care targeting opioid use and comorbidity. This intervention will use the Emergency Department Information Exchange (EDIE) to re-engage patients with subsequent ED visits. This study team developed the 'Emergency Department Longitudinal Integrated Care 2.0' intervention or 'ED-LINC' for patients with OUD to be initiated from the ED. In prior work, ED-LINC was feasible and retention in the study was high in both an intervention arm and a usual care control arm. Additionally, participants randomized to the ED-LINC arm were satisfied and acceptability of the intervention was high. Elements of ED-LINC are based on evidence-based treatments and are central components of collaborative care and will acknowledge the longitudinal care required for opioid use disorder and related substance abuse, mental health and medical comorbidity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Use Disorder
Keywords
collaborative care, opioid use disorder (OUD), substance use disorder

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized to either usual care (n=250) or ED-LINC intervention (n=250). Patients assigned to the ED-LINC intervention will receive 1) overdose education, 2) brief bedside intervention targeting motivation to engage in outpatient care, 3) a patient-centered approach to MOUD using a treatment decision support tool, 4) longitudinal and proactive care management which will proceed for 3 months, and 5) weekly caseload supervision allowing for stepped-up care targeting opioid use and comorbidity.
Masking
None (Open Label)
Masking Description
Due to the nature of the intervention, this is an open label study since participants will know whether they are receiving ED-LINC resources or usual care.
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Participants assigned to this arm will receive usual care.
Arm Title
ED-LINC Intervention
Arm Type
Experimental
Arm Description
Patients assigned to the ED-LINC intervention will receive 1) overdose education, 2) brief bedside intervention targeting motivation to engage in outpatient care, 3) a patient-centered approach to MOUD using a treatment decision support tool, 4) longitudinal and proactive care management and 5) weekly caseload supervision allowing for stepped-up care targeting opioid use and comorbidity.
Intervention Type
Other
Intervention Name(s)
ED-LINC
Other Intervention Name(s)
Collaborative Care
Intervention Description
The ED-LINC intervention provides 1) overdose education, 2) brief bedside intervention targeting motivation to engage in outpatient care, 3) a patient-centered approach to MOUD using a treatment decision support tool, 4) longitudinal and proactive care management which will proceed for 3 months, and 5) weekly caseload supervision allowing for stepped-up care targeting opioid use and comorbidity.
Primary Outcome Measure Information:
Title
Change in Illicit Opioid Use Over Time
Description
To compare self-reported past-30 day illicit opioid use using the validated self-report measure of timeline followback (TLFB) in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit.
Time Frame
Baseline ED visit and 1, 3, 6 and 12-months after ED visit
Title
Initiation of Medications for OUD
Description
To compare the frequency of initiation of medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD at scheduled follow-up intervals.
Time Frame
12 months
Title
Change in Emergency Department visits
Description
To compare changes over time in Emergency Department visits in subjects receiving usual care or ED-LINC intervention; Emergency Department visits will be measured by the Emergency Department Information Exchange (an automated health information exchange) that caputures population-level Emergency Department utilization for all enrolled participants.
Time Frame
Index Emergency Department visit to 12-months followup
Secondary Outcome Measure Information:
Title
Intervention effect when associated with Methamphetamine use
Description
Explore the impact of methamphetamine use, as measured by the timeline follow-back (TLFB) which is a validated patient self-report measure of days of methamphetamine use over a 30 day-period, on intervention treatment effects.
Time Frame
Index Emergency Department visit to 12-months followup
Title
Time to Initiation of MOUD
Description
To compare time to initiation of medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit.
Time Frame
12 months
Title
Engagement in Medications for OUD
Description
To compare the frequency of engagement in medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC over the course of the year after the index Emergency Department visit using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD at scheduled follow-up intervals.
Time Frame
12 months
Title
Retention in Medications for OUD
Description
To compare the frequency of retention in medications for opioid use disorder (MOUD) where MOUD includes buprenorphine, methadone and/or naltexone in subjects receiving usual care or ED-LINC intervention over the course of the year after the index Emergency Department visit visit using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD at scheduled follow-up intervals.
Time Frame
12 months
Title
Intervention effect when associated depression
Description
Explore the impact of depression in the past 30-days as measured by self-report PHQ-9 at baseline on intervention treatment effects.
Time Frame
Index Emergency Department visit to 12-months followup
Title
Intervention effect when associated anxiety
Description
Explore the impact of anxiety in the past 30-days as measured by self-report GAD-7 at baseline on intervention treatment effects.
Time Frame
Index Emergency Department visit to 12-months followup
Title
Intervention effect when associated PTSD
Description
Explore the impact of PTSD in the past 30-days as measured by self-report PCL-C at baseline on intervention treatment effects.baseline on intervention treatment effects.
Time Frame
Index Emergency Department visit to 12-months followup
Title
Intervention effect when associated current pain
Description
Explore the impact of pain in the past week as measured by the self-report 3-item PEG at baseline on intervention treatment effects.
Time Frame
Index Emergency Department visit to 12-months followup
Title
Intervention effect when patient has exposure to MOUD in prior 12 months
Description
Explore the impact of any past 12-month MOUD exposure prior to enrollment where MOUD includes buprenorphine, methadone and/or naltexone assessed from review of medical records, using statewide data for prescriptions and Medicaid billing data for medication administration augmented with patient self-report MOUD obtained at baseline on the intervention treatment effect.
Time Frame
Index Emergency Department visit to 12-months followup
Title
Intervention effect by sex
Description
Explore the impact of patient sex as measured by patient self-report at baseline on intervention treatment effects
Time Frame
Index Emergency Department visit to 12-months followup
Title
Intervention effect when patient reports using illicit fentanyl at baseline
Description
Explore the impact of fentanyl use as measured by any patient self-report fentanyl use in the past 30-days at baseline on the intervention treatment effect
Time Frame
Index Emergency Department visit to 12-months followup

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 18 years or older Moderate or Severe OUD based on the Structured Clinical Interview for DSM Disorders (SCID) Currently have a phone or method of contact Able to provide a phone number and one additional piece of contact information Exclusion Criteria: Incarcerated or under arrest Non-English speaking Live beyond a 50 mile radius of Harborview Medical Center Require active resuscitation in the ED or other clinical area at the time of Research Assistant (RA) approach Are receiving palliative care services or hospice care for a chronic illness such as metastatic cancer Are in the ED or hospital for a primary psychiatric emergency such as suicidal ideation or attempt and require emergent evaluation by a Psychiatrist Receiving chronic opioid therapy (COT) defined as prescription opioids for most days out of the last 90 days for a chronic pain condition In the ED for sexual assault Enrolled or eligible for state-funded or hospital-funded care coordination program based on high utilization of the ED
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Layla A Anderson
Phone
206-744-2556
Email
anderla@uw.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lauren K Whiteside, MD, MS
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harborview Medical Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lauren Whiteside
Phone
206-744-8464
Email
laurenkw@uw.edu

12. IPD Sharing Statement

Learn more about this trial

The Emergency Department Longitudinal Integrated Care

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