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Suboxone Dispenser for OUD

Primary Purpose

Opioid Use Disorder, Opioid Withdrawal

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Addinex
Sponsored by
Addinex Technologies, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid Use Disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: A minimum of 18 years old at admission of study Primary or secondary diagnosis of opioid use disorder (DSM-5; APA, 2013) diagnosis by clinician Prospective patients have to select 'Yes' they are interested in Yale-approved research studies while enrolled at Aware Recovery Care and that researchers can contact them about research projects Exclusion Criteria: Meets criterion of DSM-V (APA, 2013) for bi-polar, schizophrenia, or psychiatric disorders Unable to read and understand English at 5th grade level Unable to complete the study because of anticipated incarceration or move Life threatening or unstable medical problems Current suicide or homicide risk Anticipated/current pregnancy, or breastfeeding

Sites / Locations

  • Aware Recovery CareRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Control

Active - App

Active - Text Messaging

Arm Description

Patients in this arm will undergo standard at-home OUD treatment (n = 20/group) over 30-days.

Patients in this arm will undergo standard at-home OUD treatment in combination with the Addinex dispenser and app (n = 20/group) over 30-days.

Patients in this arm will undergo standard at-home OUD treatment in combination with the Addinex dispenser and texting (n = 20/group) over 30-days.

Outcomes

Primary Outcome Measures

Drug Test for Opioid Use Disorder (Quest 12-Panel Drug Screen)
Urine analysis will be completed on a biweekly basis for the research study

Secondary Outcome Measures

PROMIS Self-Efficacy Scale
Evaluation of participants' self-efficacy toward change over the course of the study

Full Information

First Posted
February 24, 2023
Last Updated
March 17, 2023
Sponsor
Addinex Technologies, Inc.
Collaborators
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT05790551
Brief Title
Suboxone Dispenser for OUD
Official Title
Development of a Telehealth Medication-assisted Treatment (MAT) System for Patients With Opioid Use Disorder (OUD)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 24, 2023 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Addinex Technologies, Inc.
Collaborators
Centers for Disease Control and Prevention

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to evaluate the usability and acceptability of the Addinex system with patients receiving Suboxone in OUD treatment. The main questions it aims to answer are: Are patients more likely to stay on their medication? Is the risk of diversion being reduced? How is the usability of the Addinex system for doctors and patients?
Detailed Description
Prescription opioids remain a popular drug class with 142 million (M) opioid prescriptions written in 2020. In that same year, 9.5M people aged 12 or older misused opioids representing 3.3% of that population and overdose deaths from opioids rose to 70,029, an increase of 37% (which has since increased to 82,310 in 2021). The COVID-19 pandemic has exposed many vulnerabilities in the treatment of patients with OUD. Of patients prescribed opioids, between 3-10% will later develop opioid use disorder (OUD). Given that prescription opioids remain the dominant route through which OUD begins, reducing their abuse and diversion can translate over time into reduced deaths. Many patients with OUD are treated by a combination of buprenorphine with counseling and behavioral therapies, also known as Medication Assisted Treatment (MAT). Although buprenorphine is less addictive than opioids or other treatments (e.g., methadone), it is not invulnerable to abuse or diversion. There is therefore a significant opportunity for the development of new technologies aimed at remotely treating OUD, and preventing drug misuse, abuse, and diversion. Although several secure dispenser technologies are under development, there remains a critical need for a comprehensive solution that prevents and/or treats addiction, tracks usage, collects data, and eliminates excess medication, while also remaining modular and cost effective enough to be widely accessible. Addinex Technologies, Inc. is developing the only solution that combines: 1) a patented, secure, low-cost and modular medication-dispenser which controls medication access and encourages convenient and safe unused medication disposal, combined with 2) companion mobile patient app and physician/pharmacist web-based software that features interactive modules and surveys to improve patient education and engagement, caregiver monitoring, and teletherapy to facilitate patient-provider interactions. Addinex will conduct a feasibility and acceptability study for its app-based and text-based system across patients (n = 60) undergoing OUD treatment. Successful completion of these aims will provide critical insights to further optimize the Addinex system and to guide the design of a larger, randomized controlled trial to demonstrate its efficacy and cost effectiveness. This study will be the springboard for the development of a system that is cost efficient, widely accessible, and user-friendly, with the aim of increasing adherence, decreasing treatment time, decreasing the misuse of medication, increasing treatment retention, and reducing relapses in OUD treatment for the many who are suffering.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Use Disorder, Opioid Withdrawal

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
Patients in this arm will undergo standard at-home OUD treatment (n = 20/group) over 30-days.
Arm Title
Active - App
Arm Type
Experimental
Arm Description
Patients in this arm will undergo standard at-home OUD treatment in combination with the Addinex dispenser and app (n = 20/group) over 30-days.
Arm Title
Active - Text Messaging
Arm Type
Experimental
Arm Description
Patients in this arm will undergo standard at-home OUD treatment in combination with the Addinex dispenser and texting (n = 20/group) over 30-days.
Intervention Type
Device
Intervention Name(s)
Addinex
Intervention Description
Medication dispensing system for Suboxone
Primary Outcome Measure Information:
Title
Drug Test for Opioid Use Disorder (Quest 12-Panel Drug Screen)
Description
Urine analysis will be completed on a biweekly basis for the research study
Time Frame
Up to four weeks
Secondary Outcome Measure Information:
Title
PROMIS Self-Efficacy Scale
Description
Evaluation of participants' self-efficacy toward change over the course of the study
Time Frame
Up to four weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A minimum of 18 years old at admission of study Primary or secondary diagnosis of opioid use disorder (DSM-5; APA, 2013) diagnosis by clinician Prospective patients have to select 'Yes' they are interested in Yale-approved research studies while enrolled at Aware Recovery Care and that researchers can contact them about research projects Exclusion Criteria: Meets criterion of DSM-V (APA, 2013) for bi-polar, schizophrenia, or psychiatric disorders Unable to read and understand English at 5th grade level Unable to complete the study because of anticipated incarceration or move Life threatening or unstable medical problems Current suicide or homicide risk Anticipated/current pregnancy, or breastfeeding
Facility Information:
Facility Name
Aware Recovery Care
City
North Haven
State/Province
Connecticut
ZIP/Postal Code
06473
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shelley Halligan, DNP
Phone
203-292-0980
Email
bhernandez@awarerecoverycare.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Suboxone Dispenser for OUD

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