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Technology for MAT in Primary Care - Phase 2

Primary Purpose

Opioid-use Disorder

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Opioid Addiction Recovery Support Software Platform
Sponsored by
Q2i, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Opioid-use Disorder focused on measuring Opioid use disorder, Primary care, mHealth, Medication for opioid use disorder, Technological solutions

Eligibility Criteria

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

Inclusion Criteria:

  • For Primary Care Providers (PCPs):

    • Physician, nurse practitioner, or physician's assistant in any area within primary care;
    • In possession of valid DATA-2000 waiver;
    • Currently treating more than two patients with OUD using oral buprenorphine-naloxone product;
    • Willing to distribute study materials to their patients describing the research and providing options for their participation.
  • For Patient participants:

    • Diagnosed and treated using MAT within primary care setting (i.e., family medicine, internal medicine, adolescent medicine, pediatrics, obstetrics/gynecology, geriatrics, infectious diseases, emergency department, non-cancer pain management).

Exclusion Criteria:

  • For PCPs:

    • Specialization outside primary care (e.g., psychiatry, neurology, etc) or provider works in specialized setting (e.g., addiction treatment programs; mental health clinic);
    • Not treating patients with OUD with oral buprenorphine-naloxone product (e.g., long-acting naltrexone or buprenorphine injections);
    • Individual interviews with physicians and their patients to discuss initially barriers and challenges to MAT for patients with OUD seen in primary care settings.
  • For Patient participants:

    • MAT delivered in specialty care settings (i.e., psychiatry, substance abuse treatment programs).

Sites / Locations

  • UCLA Center for Behavioral and Addiction Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

Opioid Addiction Recovery Support (OARS)

Treatment as Usual

Arm Description

Data collected post-implementation of OARS in conjunction with medication for opioid use disorder (MOUD) at study sites.

Data collected at baseline before OARS in conjunction with MOUD is implemented at study sites.

Outcomes

Primary Outcome Measures

Number and result of urine screening tests for buprenorphine, opioids (heroin, synthetics, fentanyl), cocaine, methamphetamine, benzodiazepines, cannabis
Total
Number of visits scheduled and kept with PCP
Total

Secondary Outcome Measures

Number of times OARS platform initiated by provider
Total and Number per week
Use of OARS risk score per patients
Yes/No
Number of visits scheduled and kept with psychosocial providers
Total
Type of feature and level of involvement with patient mobile application features
Total and Number per week
Number of times OARS patient mobile application initiated
Total and Number per week

Full Information

First Posted
August 12, 2021
Last Updated
March 28, 2023
Sponsor
Q2i, LLC
Collaborators
University of California, Los Angeles, National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT05017272
Brief Title
Technology for MAT in Primary Care - Phase 2
Official Title
Technology Improving Success of Medication-Assisted Treatment in Primary Care - Phase 2
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
May 1, 2021 (Actual)
Primary Completion Date
May 31, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Q2i, LLC
Collaborators
University of California, Los Angeles, National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
With over 72,000 overdose deaths in 2017, of which 47,600 are attributable to opioid overdose, the opioid epidemic has become North America's most widespread behavioral public health problem. Medication-assisted treatment (MAT) for opioid use disorder (OUD) is highly efficacious. The Opioid Addiction Recovery Support (OARS), comprised of a healthcare team portal connected to a patient mobile application, provides opioid-related education, promotes connectedness with clinicians, and tracks MAT treatment progress. This study will conduct interviews with patients that will inform optimal design of OARS, assess the efficacy of OARS in improving MAT outcomes in primary care settings, and evaluate the sustainability and return on investment. It joins an outstanding scientific team at University of California, Los Angeles and a small business that has developed, Opioid Addiction Recovery Support (OARS) -- a software platform that by integrating with the Electronic Health Record (EHR) improves clinical management of patients by primary care providers (PCPs) treating patients with OUD using MAT. OARS platform uses a dashboard to show the real-time measurement of patient achievements in recovery. It provides opportunities for patients to interact with their PCPs, allowing for better connection to and support from their PCPs. OARS platform features artificial intelligence to analyze information from the EHR and from patients to provide a relapse risk assessment for patients receiving MAT for OUD, an innovation that sets OARS apart from other software solutions. The goal of Phase 1 was to modify the OARS platform for use in primary care settings by conducting interviews with Primary Care Physicians (PCPs) (N=20) and their patients with OUD (N=40) in primary care settings to collect data on feasibility and acceptability of engaging with OARS to inform the user-centered design of OARS. The goals of Phase 2 of this study are to: (1) to assess the effectiveness of OARS in improving opioid agonist treatment outcomes across 6 treatment programs (N=200 treated patients) and (2) evaluate the sustainability and return on investment of OARS implementation across 6 treatment programs. A commercialization plan documents progress to date for the OARS platform and presents a market plan to improve both the scale and quality of MAT services delivered by PCPs in primary care, which is a major contribution to addressing the ongoing opioid epidemic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid-use Disorder
Keywords
Opioid use disorder, Primary care, mHealth, Medication for opioid use disorder, Technological solutions

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Using a "stepped wedge" effectiveness design, evaluate OARS platform in 6 treatment programs (N=200 treated patients) data before and after implementation along MAT outcomes. Each clinic, once randomized to begin using OARS, will have a minimum of 4 months and a maximum of 12 months to collect baseline data on the number of PCPs who have DATA-2000 waivers, on the number of patients each PCP treats and on relevant patient outcomes to MAT (e.g., length of time in treatment, visits kept with PCP and psychosocial providers, number of drug-free urine tests). There will be four months of baseline data available for PCPs and patients defined as treatment as usual (TAU) for clinics 1 and 2, eight months of baseline data available for PCPs and patients defined as TAU for clinics 3 and 4 and 12 months of baseline data available for PCPs and patients defined as TAU for clinics 5 and 6. In the final 3 months, we will finish data analyses, prepare papers for dissemination in peer-reviewed journals.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Opioid Addiction Recovery Support (OARS)
Arm Type
Active Comparator
Arm Description
Data collected post-implementation of OARS in conjunction with medication for opioid use disorder (MOUD) at study sites.
Arm Title
Treatment as Usual
Arm Type
No Intervention
Arm Description
Data collected at baseline before OARS in conjunction with MOUD is implemented at study sites.
Intervention Type
Other
Intervention Name(s)
Opioid Addiction Recovery Support Software Platform
Other Intervention Name(s)
OARS
Intervention Description
OARS (Opioid Addiction Recovery Support) is used by providers of MAT programs to improve insight into a patient's recovery progress while promoting ownership and adherence to treatment plans. OARS also provides extensive tools to support patients with recovery from Opioid Use Disorder.
Primary Outcome Measure Information:
Title
Number and result of urine screening tests for buprenorphine, opioids (heroin, synthetics, fentanyl), cocaine, methamphetamine, benzodiazepines, cannabis
Description
Total
Time Frame
Change from baseline treatment as usual (TAU) at post-intervention (from start of intervention through to study completion, up to 10 months)
Title
Number of visits scheduled and kept with PCP
Description
Total
Time Frame
Change from baseline treatment as usual (TAU) at post-intervention (from start of intervention through to study completion, up to 10 months)
Secondary Outcome Measure Information:
Title
Number of times OARS platform initiated by provider
Description
Total and Number per week
Time Frame
Post (OARS) intervention through to study completion, up to 10 months
Title
Use of OARS risk score per patients
Description
Yes/No
Time Frame
Post (OARS) intervention through to study completion, up to 10 months
Title
Number of visits scheduled and kept with psychosocial providers
Description
Total
Time Frame
Change from baseline treatment as usual (TAU) at post-intervention (from start of intervention through to study completion, up to 10 months)
Title
Type of feature and level of involvement with patient mobile application features
Description
Total and Number per week
Time Frame
Post (OARS) intervention through to study completion, up to 10 months
Title
Number of times OARS patient mobile application initiated
Description
Total and Number per week
Time Frame
Post (OARS) intervention through to study completion, up to 10 months
Other Pre-specified Outcome Measures:
Title
Return on Investment (ROI)
Description
ROI for a MAT provider using OARS compared to treatment as usual.
Time Frame
Post (OARS) intervention through to study completion, up to 10 months
Title
Counts of services/medications received by patients
Description
Including but not limited to visits, medications filled, reminder calls, asynchronous video related to OUD care
Time Frame
Change from baseline treatment as usual (TAU) at post-intervention (from start of intervention through to study completion, up to 10 months)
Title
Additional healthcare utilization by patients
Description
Number of Emergency Department visits, Number of Medicaid charges, Number of inpatient stays, Number of other medications
Time Frame
Change from baseline treatment as usual (TAU) at post-intervention (from start of intervention through to study completion, up to 10 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: For Primary Care Providers (PCPs): Physician, nurse practitioner, or physician's assistant in any area within primary care; In possession of valid DATA-2000 waiver; Currently treating more than two patients with OUD using oral buprenorphine-naloxone product; Willing to distribute study materials to their patients describing the research and providing options for their participation. For Patient participants: Diagnosed and treated using MAT within primary care setting (i.e., family medicine, internal medicine, adolescent medicine, pediatrics, obstetrics/gynecology, geriatrics, infectious diseases, emergency department, non-cancer pain management). Exclusion Criteria: For PCPs: Specialization outside primary care (e.g., psychiatry, neurology, etc) or provider works in specialized setting (e.g., addiction treatment programs; mental health clinic); Not treating patients with OUD with oral buprenorphine-naloxone product (e.g., long-acting naltrexone or buprenorphine injections); Individual interviews with physicians and their patients to discuss initially barriers and challenges to MAT for patients with OUD seen in primary care settings. For Patient participants: MAT delivered in specialty care settings (i.e., psychiatry, substance abuse treatment programs).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven J Shoptaw, PhD
Organizational Affiliation
University of California, Los Angeles
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCLA Center for Behavioral and Addiction Medicine
City
Los Angeles
State/Province
California
ZIP/Postal Code
90024
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://q2i.com/oars/
Description
Further information about the OARS solution available here.

Learn more about this trial

Technology for MAT in Primary Care - Phase 2

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