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COMPLETED NA

SMART Trial for Buprenorphine-Naloxone Medication Assisted Treatment Adherence

NCT04080180 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the effectiveness of two different interventions for medication-assisted treatment (MAT) adherence: Contingency Management (CM) and Brief Motivational Interviewing + Substance Free Activities + Mindfulness (BSM).

Conditions Studied

Interventions

  • BEHAVIORAL Contingency Management
  • BEHAVIORAL Brief Motivational Interviewing + Substance Free Activities + Mindfulness

Study Locations (1)

Tennessee

  • University of Tennessee Health Science Center — Memphis

Trial Details

FieldValue
Enrollment Target 332 participants
Start Date 2022-02-01
Est. Completion 2025-02-01
Phase NA

Sponsor

Karen Derefinko, PhD

2 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04080180

The ClinicalTrials.gov registry entry for NCT04080180 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 332 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Karen Derefinko, PhD, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Opioid-use Disorder appearing as the primary indexed condition, and to 2 interventions — of which Contingency Management is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04080180 reports 1 study location spanning 1 distinct geographic area — top geographies include Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04080180 about?

NCT04080180 is a clinical study titled "SMART Trial for Buprenorphine-Naloxone Medication Assisted Treatment Adherence". The purpose of this study is to compare the effectiveness of two different interventions for medication-assisted treatment (MAT) adherence: Contingency Management (CM) and Brief Motivational Interviewing + Substance Free Activities + Mindfulness (BSM).

What is the current status of trial NCT04080180?

This trial is currently completed. It is a NA study. The enrollment target is 332 participants. The study started on 2022-02-01. Estimated completion is 2025-02-01.

What conditions does trial NCT04080180 study?

This clinical trial studies the following conditions: Opioid-use Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04080180?

The interventions under investigation include: Contingency Management (BEHAVIORAL), Brief Motivational Interviewing + Substance Free Activities + Mindfulness (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04080180?

This trial is sponsored by Karen Derefinko, PhD, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04080180 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial