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Integrated e-Health (Electronic Health) for HIV and Substance Use Disorders in Justice Involved Women

Primary Purpose

HIV, Opioid Use Disorder, eHealth

Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Decision Aid
Athena strategy
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV

Eligibility Criteria

18 Years - 49 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • cis-women
  • have access to a working mobile or landline phone
  • CJ-involved (currently on probation, parole, intensive pretrial or community supervision, or are within 60 days after release from prison/jail
  • are confirmed HIV-negative by point-of-care 4th generation HIV Ag/Ab test
  • meet clinical criteria for PrEP
  • have opioid use disorder (regardless of baseline treatment status)

Exclusion Criteria:

  • unable or unwilling to provide informed consent
  • pregnant or breast-feeding
  • currently taking PrEP at the time of study enrollment
  • not comfortable conversing in English or Spanish.

Sites / Locations

  • University of Alabama in Birmingham
  • Yale UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Athena Strategy

Decision Aid

Arm Description

Virtual care model that includes direct synchronous videoconferencing with a provider, telephone/ texting communication, electronic health records, e-prescribing for the purposes of delivering PrEP and medications for opioid use disorder. This is combined with a decision aid for PrEP

Decision aid for PrEP tailored for justice-involved women with opioid use disorder

Outcomes

Primary Outcome Measures

Number of participants who initiate PrEP
PrEP in initiation will be determined using dates of prescription and pharmacy fill and medication type (brand/generic)

Secondary Outcome Measures

Number of participants who are adherent to PrEP
PrEP adherence will be assessed using a urine assay for measuring tenofovir levels (single point of care qualitative immunoassay reflecting past 48-hour adherence), where a positive test results indicates adherence.
Number of participants who engage in opioid use disorder treatment
The opioid use disorder treatment cascade engagement is composed of and defined by: 1) initiation of medications for opioid use disorder (or other evidence-based treatment); 2) 6-month retention on treatment; and 3) remission. The study will assess for complexity of substance use disorder treatment (e.g., court mandated vs. voluntary, behavioral vs. MOUD, residential vs. outpatient, detoxification program, etc.).

Full Information

First Posted
September 15, 2022
Last Updated
October 3, 2023
Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT05547048
Brief Title
Integrated e-Health (Electronic Health) for HIV and Substance Use Disorders in Justice Involved Women
Official Title
Integrated eHealth for HIV and Substance Use Disorders in Justice Involved Women
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 10, 2023 (Actual)
Primary Completion Date
April 1, 2027 (Anticipated)
Study Completion Date
April 1, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this 2-site (CT, AL) study is to test innovative interventions to reduce stigma and improve the pre-exposure prophylaxis (PrEP) and opioid use disorder (OUD) care continua in women involved in the criminal justice system (WICJ). This study evaluates a newly validated PrEP decision aid and eHealth for integrated PrEP and MOUD compared to a decision aid-only for WICJ with OUD.
Detailed Description
Problem: There is urgent need to reach women involved in criminal justice (WICJ) for lifesaving, evidence-based PrEP and medications for OUD (MOUD), using innovative healthcare delivery models that surmount existing social and structural barriers to engagement. Purpose: This study uses a newly validated decision aid and eHealth to remotely deliver integrated PrEP and MOUD to community-based WICJ with OUD in New Haven, Connecticut (CT) and Birmingham, Alabama (AL). Methods: 250 PrEP-eligible WICJ with OUD will undergo randomization to: a) the "Athena" strategy, which includes the decision aid + eHealth for remote integrated PrEP/MOUD with a provider using outputs from the decision aid; or b) decision aid-only with referral to community-based PrEP/MOUD. Randomization will be stratified by site; past 6-month use of any stimulants; and baseline receipt of MOUD. Follow-up study assessments occur at months 1, 3, and 6. To understand implementation, the investigators will conduct population modeling and engage with relevant stakeholders through focus groups using nominal group technique and in-depth individual interviews. Aims: The Aims of the project are: 1) To compare the Athena strategy to decision aid-only in terms of patient-level engagement in the PrEP and OUD care continua, considering key site differences; and 2) To assess scale-up potential of the Athena strategy in terms of modelled long-term outcomes and how stakeholders interact with eHealth for integrated PrEP/MOUD in WICJ in two diverse epidemiological and implementation contexts (CT and AL), using standardized definitions of implementation outcomes.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
This study will compare the Athena strategy to a decision aid-only intervention.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Athena Strategy
Arm Type
Experimental
Arm Description
Virtual care model that includes direct synchronous videoconferencing with a provider, telephone/ texting communication, electronic health records, e-prescribing for the purposes of delivering PrEP and medications for opioid use disorder. This is combined with a decision aid for PrEP
Arm Title
Decision Aid
Arm Type
Active Comparator
Arm Description
Decision aid for PrEP tailored for justice-involved women with opioid use disorder
Intervention Type
Behavioral
Intervention Name(s)
Decision Aid
Intervention Description
Decision aid for PrEP tailored for justice-involved women with opioid use disorder
Intervention Type
Combination Product
Intervention Name(s)
Athena strategy
Intervention Description
eHealth for integrated PrEP/medications for opioid use disorder + decision aid
Primary Outcome Measure Information:
Title
Number of participants who initiate PrEP
Description
PrEP in initiation will be determined using dates of prescription and pharmacy fill and medication type (brand/generic)
Time Frame
up to 6 months
Secondary Outcome Measure Information:
Title
Number of participants who are adherent to PrEP
Description
PrEP adherence will be assessed using a urine assay for measuring tenofovir levels (single point of care qualitative immunoassay reflecting past 48-hour adherence), where a positive test results indicates adherence.
Time Frame
up to 6 months
Title
Number of participants who engage in opioid use disorder treatment
Description
The opioid use disorder treatment cascade engagement is composed of and defined by: 1) initiation of medications for opioid use disorder (or other evidence-based treatment); 2) 6-month retention on treatment; and 3) remission. The study will assess for complexity of substance use disorder treatment (e.g., court mandated vs. voluntary, behavioral vs. MOUD, residential vs. outpatient, detoxification program, etc.).
Time Frame
up to 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
49 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: cis-women have access to a working mobile or landline phone CJ-involved (currently on probation, parole, intensive pretrial or community supervision, or are within 60 days after release from prison/jail are confirmed HIV-negative by point-of-care 4th generation HIV Ag/Ab test meet clinical criteria for PrEP have opioid use disorder (regardless of baseline treatment status) Exclusion Criteria: unable or unwilling to provide informed consent pregnant or breast-feeding currently taking PrEP at the time of study enrollment not comfortable conversing in English or Spanish.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adrienne L Marable
Phone
(203) 737-3393
Email
gcat5@yale.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carolina Price, MPA
Organizational Affiliation
Yale University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jaimie P Meyer, MD, MS, FACP
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama in Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ellen Eaton
Phone
205-934-3411
Email
eeaton@uabmc.edu
First Name & Middle Initial & Last Name & Degree
Ellen Eaton, MD
First Name & Middle Initial & Last Name & Degree
Karen Cropsey, PsyD
Facility Name
Yale University
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carolina Price, MPA
Phone
203-499-8075
Email
carolina.price@yale.edu
First Name & Middle Initial & Last Name & Degree
Jaimie P Meyer, MD, MS, FACP
First Name & Middle Initial & Last Name & Degree
Fredrick L Altice, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Integrated e-Health (Electronic Health) for HIV and Substance Use Disorders in Justice Involved Women

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