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NCT05159362 · ClinicalTrials.gov registry record · NA

Usability Testing for the Reward-based Technology to Improve OUD Treatment

A NA study, sponsored by Q2i.

Completed
Registry status
NA
Development phase
26
Enrollment target

NCT05159362 is a NA study that has completed, run by Q2i. The registered enrollment target is 26 participants.

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The verdict

NCT05159362, a NA study, has completed, sponsored by Q2i.

COMPLETED
Registry status
NA
Development phase
26 participants
Enrollment target

Study Summary

Millions of people in the US misuse opioids each year, leading to thousands of deaths and costing billions of dollars in total economic burden. Medication assisted treatment (MAT) for opioid use disorder (OUD) is highly efficacious, but only a fraction of OUD persons access MAT, and treatment non-adherence is common and associated with poor outcomes. This STTR Fast Track proposal is designed to increase rates of Suboxone (buprenorphine/naloxone) treatment initiation and adherence among OUD patients recruited from emergency and inpatient acute care. To accomplish these aims, the project will enhance the Opioid Addiction Recovery Support (OARS), an existing Q2i company technology, with a new evidence-based reward, contingency management (CM) function. CM interventions systematically reward (reinforce) specific behaviors like treatment initiation and adherence with therapy attendance and drug-free urine tests and are highly efficacious. An OARS solution enhanced with a CM component (OARSCM) that allows for the automatic calculation, delivery, and redemption of rewards contingent on objective evidence of treatment behaviors may be key to improving Suboxone initiation and adherence. In Phase 1 of this proposal, the existing OARS clinician portal and patient mobile application will be modified to accommodate entry into the software system from an acute care setting and to automatically manage and deliver rewards to create OARSCM using patient-centered design principles. Focus groups with OUD patients and other key stakeholders will inform design. Primary usability outcomes will be examined, and the program iteratively updated. After meeting milestones, there was a proof-of-concept pilot of usability, acceptability, and effects on initial behavior targets with approximately 20 patients and at least 4 providers.

Interventions

  • OTHER Software Application

Trial Details

FieldValue
Enrollment Target 26 participants
Start Date 2020-07-01
Est. Completion 2021-03-01
Phase NA

Sponsor

Q2i

4 total trials

What the Registry Record Tells You About NCT05159362

The ClinicalTrials.gov registry entry for NCT05159362 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Q2i, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Software Application is the first listed.

NCT05159362 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05159362 about?

NCT05159362 is a clinical study titled "Usability Testing for the Reward-based Technology to Improve OUD Treatment". Millions of people in the US misuse opioids each year, leading to thousands of deaths and costing billions of dollars in total economic burden. Medication assisted treatment (MAT) for opioid use disorder (OUD) is highly efficacious, but only a fraction of OUD persons access MAT, and treatment non-ad...

What is the current status of trial NCT05159362?

This trial is currently completed. It is a NA study. The enrollment target is 26 participants. The study started on 2020-07-01. Estimated completion is 2021-03-01.

What interventions are being tested in trial NCT05159362?

The interventions under investigation include: Software Application (OTHER).

Who is sponsoring clinical trial NCT05159362?

This trial is sponsored by Q2i, which has 4 total clinical trials registered on ClinicalTrials.gov.

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

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