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Clinical Trials/NCT04111939
NCT04111939
Active, not recruiting
Not Applicable

HEALing Communities Study: Developing and Testing an Integrated Approach to Address the Opioid Crisis

RTI International4 sites in 1 country67 target enrollmentOctober 23, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Opioid Use Disorder (OUD)
Sponsor
RTI International
Enrollment
67
Locations
4
Primary Endpoint
Number of Opioid Overdose Deaths
Status
Active, not recruiting
Last Updated
11 months ago

Overview

Brief Summary

This study will test the impact of implementing the Communities That Helping to End Addiction Long-term (HEAL) intervention on opioid overdose deaths within 67 highly affected communities with the goal of reducing opioid overdose deaths by 40%.

Detailed Description

The HEALing Communities Study (HCS) is a multi-site, parallel group, cluster randomized wait-list controlled trial to test the impact of the Communities That HEAL (CTH) intervention, which is designed to increase the adoption of an integrated set of evidence-based practices delivered across healthcare, behavioral health, justice, and other community-based settings. The intervention will include 3 components: community engagement to assist key stakeholders in applying evidence-based practices to addressing their opioid crisis, a menu of evidence-based practices for communities to select and implement, and a communications campaign to build demand for evidence-based practices to address overdose and opioid use disorder. Communities receiving the intervention will be engaged to reach individuals who are at highest risk of overdose death (e.g., out of treatment, leaving jail) and: (1) expand access to and receipt of medication for opioid use disorder (MOUD) and behavioral treatment, (2) increase the number of individuals retained in treatment beyond 6 months, (3) reduce the risk of fatal overdose through expansion of overdose education and naloxone distribution, and (4) improve prescription opioid safety. In addition, the study will determine (1) the factors that contribute to or impede successful implementation of the CTH intervention, (2) the factors that contribute to or impede sustainment of CTH intervention, and (3) the incremental costs and cost effectiveness of the CTH intervention.

Registry
clinicaltrials.gov
Start Date
October 23, 2019
End Date
September 30, 2025
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The community must be located in one of the four participating states: Kentucky, Ohio, Massachusetts, or New York.
  • At least 30% of the communities selected within each state must be rural.
  • Across all the HCS communities within each state, there must be a minimum of 150 opioid-related overdose fatalities (with at least 22 opioid-related overdose fatalities experienced by the rural communities) and a rate of at least 25 opioid-related overdose fatalities per 100,000 persons, based on 2016 data.
  • The community must express willingness to address in their response strategy the implementation of MOUD, overdose prevention training, and naloxone distribution across their community.
  • The community must express willingness to develop partnerships across health care, behavioral health, and justice settings for evidence-based practices to address opioid misuse, OUD, and overdoses.

Exclusion Criteria

  • Communities that did not meet the aforementioned inclusion criteria were excluded from the HCS.

Outcomes

Primary Outcomes

Number of Opioid Overdose Deaths

Time Frame: Months 19-30

Count of HCS community resident overdose deaths (i.e. deaths with an underlying cause of drug poisoning) where opioids were determined to be contributing (alone or in combination with other drugs) to the drug poisoning.

Secondary Outcomes

  • Number of Naloxone Units Distributed in Communities(Months 19-30)
  • Number of Individuals Receiving Buprenorphine Products That Are Approved by the Food and Drug Administration (FDA) for Treatment of OUD(Months 19-30)
  • Incidents of High-risk Opioid Prescribing(Months 19-30)

Study Sites (4)

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