Emergency Department Connection to Care With Buprenorphine for Opioid Use Disorder

Opioid-use Disorder Clinical Trial

— ED-CONNECT  

Official title:

NIDA CTN-0079: Emergency Department Connection to Care With Buprenorphine for Opioid Use Disorder

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03544112
• Other study ID #: 17-01513
• Status: Completed
• Start date: June 11, 2018
• Est. completion date: May 29, 2019

Study information

• Verified date: August 2019
• Source: NYU Langone Health
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of this study is to learn what resources are needed to improve outcomes for patients with opioid use disorder. The study will look at how patients engage in treatment and the decisions that patients and providers make regarding treatment, specifically buprenorphine treatment, for opioid use disorder.

The aims of this study are:

1. To evaluate using mixed methods the feasibility and acceptability of OUD screening, ED-initiated BUP, and referral.

2. Over the course of the study and as XR-BUP is added to hospital formularies, to estimate the percentage and confidence intervals of patients assessed, treated, and engaged in treatment at Day 30. This will be a three-site study employing a multi-faceted approach to facilitate clinical protocol implementation and to assess feasibility, acceptability, and impact. Investigators will develop, introduce and update site-specific ED clinical protocols and implementation plans for OUD screening, ED-initiated BUP, and referral for treatment. A participatory action research approach will be utilized along with mixed methods incorporating data derived from:

• Medical record and administrative data abstraction,

• Research assessments involving patients who are eligible for and willing to receive ED-initiated BUP (including both those who do, and do not, receive BUP); these assessments will document the index ED visit and the 30th day after the index ED visit,

• Qualitative interviews, focus groups, and quantitative assessments involving providers and staff, patients, and other stakeholders.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 390
• Est. completion date: May 29, 2019
• Est. primary completion date: May 29, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• ED STAFF: ED/Hospital leadership and staff: Leadership and staff across multiple disciplines (e.g., nurses, social workers, physicians, NPs, PAs, pharmacist, physician and nursing directors) at each ED site will be recruited to participate in the formative evaluation and the IF.

• PROVIDERS: Community treatment providers/OTP leadership and program staff: Providers, leadership and staff involved in the provision of office-based BUP, community treatment, and/or at opioid treatment programs (OTPs) will be recruited to participate in the formative evaluation and the Implementation Facilitation.

• COMMUNITY: Other Stakeholders: Other community leaders and members (e.g., EMS, fire department, police, local government leadership, community advocacy groups, etc.) may be recruited to participate in qualitative interviews or focus groups.

• PATIENTS: ED patients will be recruited to participate in interviews or focus groups.

• PATIENT-PARTICIPANTS: ED patients who are eligible for and willing to receive ED-initiated BUP will be recruited to participate in two research visits.

• ALL ED PATIENTS: Administrative and health record data will be examined to assess rates of screening, assessment, eligibility determination, etc.

Stakeholder-Participant Inclusion Criteria

• A member of one of the stakeholder groups (1-4 above)

Patient-Participant Inclusion Criteria

• Eligible for and willing to receive ED-initiated BUP

1. Eligibility for ED-initiated BUP is operationally defined as meeting site clinical protocol criteria determined and documented by site clinical staff. See Section 9.2 Clinical Protocol.

2. Willing to receive ED-initiated BUP is operationally defined as providing an affirmative answer to the following question, which will be embedded in each site's clinical protocol: Would you like to receive buprenorphine today?

3. NOTE: Patients meeting these criteria, and not meeting exclusion criteria below, may be included as study participants regardless of whether they receive or do not receive ED-initiated BUP

Exclusion Criteria:

Stakeholder-Participant Exclusion Criteria

• Unwilling or unable to provide consent

• Currently in jail, prison or any inpatient overnight facility as required by court of law or have pending legal action or that could prevent participation in the study

Patient-Participant Exclusion Criteria

• Not able to speak English sufficiently to understand study procedures and provide written informed consent

• Unable or unwilling to provide written informed consent or to participate in study procedures

• Currently receiving any medication treatment for OUD at the time of index ED visit

• Current research participant in a substance use intervention study or previous participation in the current study

• Are currently in jail, prison or any inpatient overnight facility as required by court of law or have pending legal action or that could prevent participation in the study

• Inadequate locator information (unable to provide 2 unique means of contact)

Related Conditions & MeSH terms

• Disease
• Emergencies
• Opioid-use Disorder
• Substance-Related Disorders

Intervention

Behavioral:
• Employ a multifaceted approach to facilitate clinical protocol implementation
Implementation will include developing clinical protocols containing core components of the intervention to which fidelity is expected, along with aspects that may be adapted by local sites to aid implementation. In partnership with multidisciplinary teams at each site, we will adapt clinical practices from other contexts and available information about SL-BUP and XR-BUP to site-specific clinical protocols and implementation strategies. The study implementation facilitators will assist local champions to identify potential treatment providers and draw on existing resources for training and ongoing support.

Drug:
• Initiate BUP (SL-BUP or XR-BUP) in the ED
The study implementation facilitators will assist local champions to identify potential treatment providers and draw on existing resources for training and ongoing support.

Locations

Country	Name	City	State
United States	Valley Regional Healthcare	Claremont	New Hampshire
United States	Catholic Medical Center	Manchester	New Hampshire
United States	Bellevue Hospital Center	New York	New York
United States	New York University School of Medicine	New York	New York

Sponsors (2)

Lead Sponsor	Collaborator
NYU Langone Health	National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Receipt of ED-initiated BUP (binary) and will be abstracted from the health record.	Proportion receiving emergency department BUP amongst patients who have been determined to be eligible for and willing to receive ED-initiated BUP	12 Months
Secondary	Proportion of patients who received ED-initiated BUP who are engaged in formal addiction treatment 30 days after the index ED visit.		12 Months