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

HIV Clinical Trial

Official title:

Integrated eHealth for HIV and Substance Use Disorders in Justice Involved Women

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05547048
• Other study ID #: 2000033006
• Secondary ID: 1R01DA057342-01
• Status: Recruiting
• Phase: Phase 3
• Start date: July 25, 2023
• Est. completion date: April 1, 2027

Study information

• Verified date: May 2024
• Source: Yale University
• Contact: Adrienne L Marable
• Phone: (203) 737-3393
• Email: gcat5[@]yale.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 250
• Est. completion date: April 1, 2027
• Est. primary completion date: April 1, 2027
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 59 Years

Eligibility

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 12 months after release from prison/jail

• are confirmed HIV-negative by point-of-care 3rd generation HIV antibody 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.

Related Conditions & MeSH terms

• eHealth
• HIV
• Opioid Use Disorder
• Opioid-Related Disorders
• Substance-Related Disorders

Intervention

Behavioral:
• Decision Aid
Decision aid for PrEP tailored for justice-involved women with opioid use disorder

Combination Product:
• Athena strategy
eHealth for integrated PrEP/medications for opioid use disorder + decision aid

Locations

Country	Name	City	State
United States	University of Alabama in Birmingham	Birmingham	Alabama
United States	Yale University	New Haven	Connecticut

Sponsors (2)

Lead Sponsor	Collaborator
Yale University	National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants who initiate PrEP	PrEP in initiation will be determined using dates of prescription and pharmacy fill and medication type (brand/generic)	up to 6 months
Secondary	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.	up to 6 months
Secondary	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.).	up to 6 months