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Connection, Navigation, Engagement in Care and Treatment for Opioid Use Disorder (ConNECT)

D

Denver Health and Hospital Authority

Status

Completed

Conditions

Opioid-use Disorder

Treatments

Behavioral: Case management

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT04797962
20-2236
R01CE00300 (Other Grant/Funding Number)

Details and patient eligibility

About

The overarching goal of the study is to develop, pilot, and evaluate an intervention that aims to retain patients who initiate buprenorphine at Denver Health in ongoing treatment for opioid use disorder.

Full description

Initiating patients identified with opioid use disorder in hospital settings onto buprenorphine is a relatively new strategy to prevent overdose. While the literature is beginning to amass showing the effectiveness of this strategy for initiating people into treatment, a dearth of data to describe how well people are maintained in treatment remains. The current research project aims to 1) develop an intervention to enhance engagement and retention in treatment for individuals with opioid use disorder who initiate buprenorphine at Denver Health and 2) assess acceptability, feasibility, and initial efficacy of an intervention to enhance engagement and retention in treatment for individuals with opioid disorder compared to usual care.

Enrollment

102 patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years and older
  • inducted onto buprenorphine at Denver Health
  • successfully completed an intake visit at Denver Health's Outpatient Behavioral Health Services clinic.

Exclusion criteria

  • unable to provide informed consent
  • unable to provide detailed contact information
  • previously enrolled in the current study
  • pregnant women will be excluded given that they are a priority treatment population and receive special services

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

102 participants in 2 patient groups

Intervention
Experimental group
Description:
dedicated case management
Treatment:
Behavioral: Case management
Usual care
No Intervention group
Description:
usual care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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