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Patient-Centered Care for Opioid Use Disorders in Federally Qualified Healthcare Centers and Specialty Care Settings

Primary Purpose

Opioid-use Disorder, Substance Use Disorders

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Individual Therapy Sessions
Cognitive Behavioral Therapy (CBT)
Medication-Assisted Treatment
Peer Recovery Specialist Support
Group Therapy Sessions
Psychiatric Consultation
Contingency Management
Sponsored by
Public Health Management Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid-use Disorder focused on measuring Federally Qualified Health Center, Contingency Management, Cognitive Behavioral Therapy, Cognitive Behavioral / Relapse Prevention, Medication Assisted Treatment, Behavioral Health Consultant, Integrated Care

Eligibility Criteria

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

Inclusion Criteria:

  1. Patient is 18 years or older
  2. As determined according to the ASAM Criteria CONTINUUM Software decision engine, patient meets criteria for: a) Level 1 care, i.e., outpatient treatment, OR b) Level 2 care, i.e., intensive outpatient treatment.

Exclusion Criteria:

  1. The medical practitioner or BHC overrule these criteria because medical and psychiatric complications exist that would contraindicate research participation
  2. Patient requires an ASAM level of care greater than Level 2
  3. The patient reports plans to leave the area (i.e. Philadelphia or Washington, DC greater metropolitan area) within the next 6 months
  4. The patient is not English-speaking
  5. The patient is unable to provide valid informed consent by correctly describing the key components of consent to the Research Assistant.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Personalized Addiction-to-Health (PATH)

    Standard Care

    Arm Description

    Cognitive Behavioral Therapy (CBT) sessions with a behavioral health consultant twice weekly for weeks 1-13, once weekly for weeks 14-26, as needed weeks 27-52; Contingency management rewards for specified recovery behaviors which could include medication adherence, attendance at CB/RP sessions and/or CB/RP exercise participation; Medication-assisted treatment, either extended-release naltrexone once monthly or buprenorphine once daily; Peer recovery specialist support twice weekly for weeks 1-13, once weekly for weeks 14-26, as needed for weeks 27-52; Psychiatric consultation as needed.

    Treatment may differ slightly by treatment program, but addiction specialty Intensive Outpatient Treatment (ASAM Level 2.1) will generally include individual therapy sessions with a counselor 1 hour per week for week; Medication-assisted treatment, either extended-release naltrexone once monthly or suboxone once daily; Group therapy sessions 9 hours per week then decreasing to 3 hours per week; Psychiatric consultation as needed.

    Outcomes

    Primary Outcome Measures

    Change in confirmed substance abstinence
    On-site urine drug testing kits rapidly test for cocaine, opiates, amphetamines, methamphetamines, benzodiazepines, cannabis, barbiturates, Phencyclidine, and alcohol. Urine testing will be administered at all follow-ups to capture use within the last 3 days.
    Change in retention in treatment
    Verify patient self-report of treatment engagement by acquiring payment data from funders. Federally Qualified Health Centers and Standard Care Intensive Outpatient programs will release study patient records to resolve inconsistencies between patient report and billing data, including treatment session attendance, medications prescribed, prescriptions filled, doses received, and results from urinalysis testing. Data will be collected for the past 3 months.

    Secondary Outcome Measures

    Lower rates of service utilization
    Patient reported service utilization including substance abuse treatment, medical services, visits to medical offices, hospitalizations, and emergency room visits received that were not a part of the assigned treatment during the past 3 months
    Higher quality of life
    Self-reported enjoyment and satisfaction experienced in various areas of daily functioning during the past week
    Lower rates of HIV risk behaviors
    Self-reported drug use, injection-related risk behavior, sexual risk, and HIV testing history and results for the past 3 months.

    Full Information

    First Posted
    November 28, 2017
    Last Updated
    June 19, 2019
    Sponsor
    Public Health Management Corporation
    Collaborators
    Patient-Centered Outcomes Research Institute
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03367234
    Brief Title
    Patient-Centered Care for Opioid Use Disorders in Federally Qualified Healthcare Centers and Specialty Care Settings
    Official Title
    A Simple Large Trial of Patient-Centered Care for Opioid Use Disorders in Federally Qualified Healthcare Centers and Specialty Care Settings
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2019
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Study experienced delays due to site recruitment. Funder terminated contract.
    Study Start Date
    July 2019 (Anticipated)
    Primary Completion Date
    June 30, 2022 (Anticipated)
    Study Completion Date
    June 30, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Public Health Management Corporation
    Collaborators
    Patient-Centered Outcomes Research Institute

    4. Oversight

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

    5. Study Description

    Brief Summary
    This study evaluates the effectiveness of integrating empirically-supported treatments for an opioid use disorder into a primary care setting. These treatments will include ASAM Criteria multidimensional assessment, cognitive behavioral therapy and relapse prevention with contingency management, medication-assisted treatment, and recovery support services. Half of participants will be assigned to opioid use disorder treatment in a federally qualified health center, and half will receive treatment at a publicly-funded intensive outpatient addiction treatment program which has the ability to offer medication-assisted treatment.
    Detailed Description
    This is a large, simple, comparative effectiveness trial of the Personalized Addiction Treatment-to-Health Model vs. standard care in the community specialty addiction treatment system. PATH combines several empirically supported treatment methods in a flexible schedule in tandem with primary care, with the goals of higher rates of confirmed substance abstinence and treatment retention. PATH components include: 1) The CONTINUUM multidimensional assessment, an evidence-based implementation of the American Society of Addiction Medicine (ASAM) placement criteria; 2) Cognitive Behavioral Relapse Prevention (CB/RP), a skills-based approach centered on teaching coping skills to handle risky situations that can be practiced and learned; 3) Contingency management (CM), which targets chronic substance use's diminution of brain dopaminergic reward by specifically conditioning positive recovery behaviors via immediate financial incentives; and 4) Recovery Support Services, non-professional community-based services for wrap-around care needs. Effect sizes for a combined CB/RP and CM approach appear to be large and there is evidence that this combination results in longer lasting improvements presumably as homeostasis returns to the reward system. An extensive literature demonstrates that counseling plus medication-assisted treatment (MAT) yields superior outcomes versus counseling alone. Buprenorphine and extended-release naltrexone are well suited for use in primary care. Buprenorphine is a partial agonist at the mu-opioid receptor that provides anti-withdrawal and anti-craving effects for up to 36 hours on a single dose. Partial agonism and a slow onset diminish the patient's perception of euphoria, limiting abuse, while the long half-life and binding duration make it useful for both detoxification and long-term opioid maintenance. Extended-release naltrexone is a once-monthly intramuscular injection that, following detoxification, provides opioid receptor blockade for at least 30 days and is safe and effective for prolonging abstinence and preventing relapse from opiates.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Opioid-use Disorder, Substance Use Disorders
    Keywords
    Federally Qualified Health Center, Contingency Management, Cognitive Behavioral Therapy, Cognitive Behavioral / Relapse Prevention, Medication Assisted Treatment, Behavioral Health Consultant, Integrated Care

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Personalized Addiction-to-Health (PATH)
    Arm Type
    Experimental
    Arm Description
    Cognitive Behavioral Therapy (CBT) sessions with a behavioral health consultant twice weekly for weeks 1-13, once weekly for weeks 14-26, as needed weeks 27-52; Contingency management rewards for specified recovery behaviors which could include medication adherence, attendance at CB/RP sessions and/or CB/RP exercise participation; Medication-assisted treatment, either extended-release naltrexone once monthly or buprenorphine once daily; Peer recovery specialist support twice weekly for weeks 1-13, once weekly for weeks 14-26, as needed for weeks 27-52; Psychiatric consultation as needed.
    Arm Title
    Standard Care
    Arm Type
    Active Comparator
    Arm Description
    Treatment may differ slightly by treatment program, but addiction specialty Intensive Outpatient Treatment (ASAM Level 2.1) will generally include individual therapy sessions with a counselor 1 hour per week for week; Medication-assisted treatment, either extended-release naltrexone once monthly or suboxone once daily; Group therapy sessions 9 hours per week then decreasing to 3 hours per week; Psychiatric consultation as needed.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Individual Therapy Sessions
    Intervention Description
    One-on-one sessions with a counselor
    Intervention Type
    Behavioral
    Intervention Name(s)
    Cognitive Behavioral Therapy (CBT)
    Other Intervention Name(s)
    CBT, CB/RP
    Intervention Description
    Cognitive Behavioral Therapy techniques delivered by a behavioral health consultant (BHC)
    Intervention Type
    Behavioral
    Intervention Name(s)
    Medication-Assisted Treatment
    Other Intervention Name(s)
    MAT
    Intervention Description
    Buprenorphine or Extended-Release Naltrexone
    Intervention Type
    Behavioral
    Intervention Name(s)
    Peer Recovery Specialist Support
    Intervention Description
    Individual and/or group sessions with a certified peer recovery specialist
    Intervention Type
    Behavioral
    Intervention Name(s)
    Group Therapy Sessions
    Intervention Description
    Group therapy sessions
    Intervention Type
    Behavioral
    Intervention Name(s)
    Psychiatric Consultation
    Intervention Description
    Access to psychiatric consultation
    Intervention Type
    Behavioral
    Intervention Name(s)
    Contingency Management
    Intervention Description
    Rewards for engagement in specified recovery behaviors
    Primary Outcome Measure Information:
    Title
    Change in confirmed substance abstinence
    Description
    On-site urine drug testing kits rapidly test for cocaine, opiates, amphetamines, methamphetamines, benzodiazepines, cannabis, barbiturates, Phencyclidine, and alcohol. Urine testing will be administered at all follow-ups to capture use within the last 3 days.
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Title
    Change in retention in treatment
    Description
    Verify patient self-report of treatment engagement by acquiring payment data from funders. Federally Qualified Health Centers and Standard Care Intensive Outpatient programs will release study patient records to resolve inconsistencies between patient report and billing data, including treatment session attendance, medications prescribed, prescriptions filled, doses received, and results from urinalysis testing. Data will be collected for the past 3 months.
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Secondary Outcome Measure Information:
    Title
    Lower rates of service utilization
    Description
    Patient reported service utilization including substance abuse treatment, medical services, visits to medical offices, hospitalizations, and emergency room visits received that were not a part of the assigned treatment during the past 3 months
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Title
    Higher quality of life
    Description
    Self-reported enjoyment and satisfaction experienced in various areas of daily functioning during the past week
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Title
    Lower rates of HIV risk behaviors
    Description
    Self-reported drug use, injection-related risk behavior, sexual risk, and HIV testing history and results for the past 3 months.
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Other Pre-specified Outcome Measures:
    Title
    Change in Employment Severity Score
    Description
    The American Society of Addiction Medicine (ASAM) Continuum is computer-guided, standardized interview for assessing and caring for patients with substance use disorders and co-occurring conditions. The employment section asks participants about their employment status during the past 3 months using questions from the Addiction Severity Index (ASI). The composite score of the ASI employment section ranges from 0-1 with higher scores indicating greater problem severity.
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Title
    Change in Family/Social Functioning Severity Score
    Description
    The American Society of Addiction Medicine (ASAM) Continuum is computer-guided, standardized interview for assessing and caring for patients with substance use disorders and co-occurring conditions. The family and social functioning section asks participants about their family and social functioning during the past 3 months using questions from the Addiction Severity Index (ASI). The composite score of the ASI family and social functioning section ranges from 0-1 with higher scores indicating greater problem severity.
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups
    Title
    Change in Psychiatric Severity Score
    Description
    The American Society of Addiction Medicine (ASAM) Continuum is computer-guided, standardized interview for assessing and caring for patients with substance use disorders and co-occurring conditions. The psychiatric section asks participants about their psychiatric functioning during the past 3 months using questions from the Addiction Severity Index (ASI). The composite score of the ASI psychiatric section ranges from 0-1 with higher scores indicating greater problem severity.
    Time Frame
    Baseline, 3-, 6-, 9-, 12-, 15-, and 18 month follow-ups

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patient is 18 years or older As determined according to the ASAM Criteria CONTINUUM Software decision engine, patient meets criteria for: a) Level 1 care, i.e., outpatient treatment, OR b) Level 2 care, i.e., intensive outpatient treatment. Exclusion Criteria: The medical practitioner or BHC overrule these criteria because medical and psychiatric complications exist that would contraindicate research participation Patient requires an ASAM level of care greater than Level 2 The patient reports plans to leave the area (i.e. Philadelphia or Washington, DC greater metropolitan area) within the next 6 months The patient is not English-speaking The patient is unable to provide valid informed consent by correctly describing the key components of consent to the Research Assistant.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    David R Gastfriend, MD
    Organizational Affiliation
    Public Health Management Corporation
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Patient-Centered Care for Opioid Use Disorders in Federally Qualified Healthcare Centers and Specialty Care Settings

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