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Cooperative Re-Engagement Controlled Trial (CoRECT)

Cooperative Re-Engagement Controlled Trial (CoRECT)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02693145
Acronym
CoRECT
Enrollment
1893
Registered
2016-02-26
Start date
2016-08-31
Completion date
2020-08-31
Last updated
2021-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Human Immunodeficiency Virus

Keywords

HIV/AIDS, re-engagement in care, data to care

Brief summary

CoRECT will help identify the important components of a data-sharing partnership between health departments and HIV care providers, and determine the extent to which a health department intervention can increase the number of HIV-infected persons out-of-care who: (a) link to an HIV clinic; (b) remain in HIV medical care; (c) achieve HIV viral load suppression within 12 months; and (d) achieve durable HIV viral load suppression over 18 months. We will also measure the cost-effectiveness of this intervention in regards to improved health in the individuals (re)-engaged in HIV care and reductions in further HIV transmission in the community.

Detailed description

Methods summary: Health departments will generate an out-of-care list using HIV laboratory surveillance data; collaborating clinics will concurrently generate out-of-care lists using appointment data. The combined out-of-care list will be reconciled by the health department and clinics, and discussed at monthly case conferences. All individuals determined to be out-of care will be randomized to receive either: (1) usual linkage and engagement in care services (standard of care \[SOC\]); or (2) an active health department field services intervention in addition to SOC. The active intervention activities will vary among jurisdictions; however all sites will include field services to locate, contact, and provide assistance, including a same-day appointment, to access HIV medical care. Study design: Each site will enroll 600 out-of-care HIV-infected individuals (300 per arm) during a two-year enrollment period. An out-of-care individual will be defined as: (1) a person who has received HIV medical care at a CoRECT clinic and then disengages from care; or (2) a person with newly diagnosed HIV infection who has an appointment at a CoRECT clinic, but has not linked to medical care within 90 days. Intervention: Individuals randomized to the intervention arm will receive field services to locate, contact, and provide assistance to access HIV medical care. Services provided as part of the intervention will vary by jurisdiction, but may include assistance with expedited medical appointments, transportation, access to community resources such as traditional case management, strengths-based case management, or financial incentives (Appendix A). Primary outcomes: The following outcomes will be compared between out-of-care HIV-infected individuals receiving the study intervention to those receiving usual services: 1. Attend 1 clinic visit within 90 days; 2. Remain engaged in care, defined as 2 clinic visits at least 3 months apart within 12 months; 3. Achieve viral load suppression within 12 months; 4. Achieve durable viral load suppression, defined as 2 consecutive suppressed viral load results at least 3 months apart within 18 months

Interventions

OTHERAnti-Retroviral Treatment and Access to Services (ARTAS)

Anti-Retroviral Treatment and Access to Services (ARTAS) is an individual-level, multi-session, time-limited intervention with the goal of linking recently diagnosed persons with HIV to medical care soon after receiving their positive test result. ARTAS is based on the Strengths-based Case Management (SBCM) model, which is rooted in Social Cognitive Theory (particularly self-efficacy) and Humanistic Psychology. SBCM is a model that encourages the client to identify and use personal strengths; create goals for himself/herself; and establish an effective, working relationship with the Linkage Coordinator (LC).

Sponsors

Connecticut State, Department of Mental Health and Addiction Services
CollaboratorOTHER_GOV
Massachusetts Department of Health
CollaboratorOTHER_GOV
Philadelphia Department of Public Health
CollaboratorOTHER_GOV
Centers for Disease Control and Prevention
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Residents within the health department jurisdiction who have received HIV medical care at a CoRECT clinic and then disengage by either of the following definitions: * Clinic definition: did not have a visit with a prescribing provider for 6 months. * Health department definition: no CD4 or viral load test result reported to health department surveillance for more than 6 months. 2. Residents within the health department jurisdiction with newly diagnosed HIV infection who have not linked to medical care within 90 days and have either: * Received, but did not attend, an appointment at a CoRECT clinic; or * Attended an enrollment visit but did not receive medical care at a CoRECT clinic.

Exclusion criteria

1. Deceased 2. Out of jurisdiction 3. Changed providers 4. Incarcerated

Design outcomes

Primary

MeasureTime frameDescription
Attend one clinic visitwithin 90 days of randomizationPatient will attend one clinical visit at CoRECT clinic to receive HIV medical care
Remain engaged in caredefined as 2 clinic visits at least 3 months apart within 12 monthsTwo or more medical visits at least 3 months apart within 12 months to demonstrate patient remains engaged in HIV medical care
Viral load suppressionwithin 12 monthsDoes the patient achieve viral load suppression within 12 months of randomization
Achieve durable viral load suppressiondefined as 2 consecutive suppressed viral load results at least 3 months apart within 18 monthsAchieve durable viral load suppression, defined as 2 consecutive suppressed viral load results at least 3 months apart within 18 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026