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NCT04982627: BNICHAT
A Brief Negotiation Interview Chatbot to Improve Buprenorphine Engagement Among Justice-Involved Individuals
NA trial testing BNI Chatbot in Opioid Use Disorder, Moderate in 4 participants. Completed in 1 September 2023.
31 August 2022
Quick facts
| Lead sponsor | Center for Progressive Recovery, LLC |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 4 |
| Start date | 1 August 2021 |
| Primary completion | 31 August 2022 |
| Estimated completion | 1 September 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- BNI Chatbot
- OUD Education & Treatment Resources
Conditions studied
- Opioid Use Disorder, Moderate — all drugs for Opioid Use Disorder, Moderate →
- Opioid Use Disorder, Severe — all drugs for Opioid Use Disorder, Severe →
- Criminal Behavior — all drugs for Criminal Behavior →
Sponsor
Center for Progressive Recovery, LLC
Who can join
Adults 18 to 65, any sex, with Opioid Use Disorder, Moderate or Opioid Use Disorder, Severe. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Primary Objective: Conduct pilot study to assess effects of brief negotiation interview (BNI) Chatbot among individuals involved in the Connecticut criminal justice system with opioid use disorder (OUD). Study Duration: Approximately 2 years (1 year for study activities, 1 year for data analysis) Study Design: This is a prospective, randomized study to evaluate the effectiveness of a BNI Chatbot on patients with OUD compared with Standard Care (SC). Number of Study Sites: The offices of the Center for Progressive Recovery, LLC and the New Haven Police Department Detention Center (NHPD). Study Population: The study population includes adult individuals with OUD who are involved in the Connecticut criminal justice system and not currently receiving medication-assisted treatment for their OUD. Number of Participants: Sixty participants Primary Outcome Variable: Attendance at participants first treatment appointment within four weeks of referral among participants in the BNI Chatbot vs. Standard Care (SC) groups. Secondary Outcome and Exploratory Outcome Variables: Secondary outcomes include readiness and intention to engage in buprenorphine (bup) treatment, and urine toxicology test-confirmed drug use at four weeks among participants in BNI Chatbot vs. SC groups. Exploratory outcomes include ratings of feasibility, acceptability and satisfaction between study groups, and a comparison of study findings to engagement data from previous in-person studies, including BNI+bup, and other digital programs, such as reSET-O, and DynamiCare.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT04982627
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Related trials
Other recruiting trials for Opioid Use Disorder, Moderate
Currently open trials in the same condition.
- NCT06651177 — Evaluation of Tirzepatide as an Adjunct to Buprenorphine for the Treatment of Opioid Use Disorder · Phase 2 · recruiting
- NCT04921787 — EXHIT ENTRE Implementation Trial of High Intensity Versus Low Intensity Strategy · NA · active not recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04982627 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Center for Progressive Recovery, LLC
- Last refreshed: 3 July 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04982627.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing