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Study of HIV, HCV, APS and Phylogenetics for PWID

Integrating Assisted Partner Services and Phylogenetics for HIV and HCV Prevention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03447210
Acronym
SHARP
Enrollment
4301
Registered
2018-02-27
Start date
2018-02-26
Completion date
2022-02-28
Last updated
2022-11-21

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

Conditions

Hepatitis C, HIV/AIDS

Keywords

Persons who inject drugs (PWID), Phylogenetics, HIV testing, HCV testing, HIV care cascade, Assisted partner services

Brief summary

This study will determine whether assisted partner notification services (APS) can identify and link to care, the sexual and needle-sharing partners of HIV-infected and HIV/hepatitis C (HCV) co-infected persons who inject drugs (PWID). It will also define the risk factors for onward HIV and HCV transmission among PWID using viral phylogenetics.

Detailed description

Overview: This NIH-funded study uses assisted partner services (APS) to identify HIV-infected and HCV-infected persons who inject drugs (PWID) in Kenya and link them to care. In addition to determining the role of APS in HIV and HCV case-finding for this hard-to-reach key population, we leverage our experience with HIV and HCV phylogenetics in the US and South Africa to define modes and risk factors for onward viral transmission. The specific aims of the proposal are as follows: AIM 1. To determine whether contact tracing and partner notification practices, known in Kenya as assisted partner services (APS), can identify and link to care, the sexual and injection partners of HIV-infected and HIV/ hepatitis C (HCV) co-infected persons who inject drugs (PWID). AIM 2. To define the risk factors for HIV transmission among PWID, and to elucidate the role of PWID in the overall Kenyan HIV epidemic, using viral genetic sequencing techniques. AIM 3. To characterize the modes and risk factors for onward HCV transmission among PWID using viral genetic sequencing. Design: We will enroll 1000 HIV-infected PWID through a needle and syringe exchange program (NSP) in Nairobi, Kenya. Each index participant will undergo a structured questionnaire, a rapid HCV test, a blood draw, and will provide locator information regarding their sexual and injection partners from the past 3 years. Study staff will then attempt to locate all partners. Once located, partner participants will undergo rapid HIV and HCV testing, a structured questionnaire, and a blood draw. All blood samples will be sent to a central laboratory in Nairobi for processing. Dried blood spot samples will be created in Nairobi and will later be sent to the University of KwaZulu-Natal for quantitative viral loads for both HIV and hepatitis C, and follow-up phylogenetic testing. All participants who test positive for HIV or hepatitis C will be referred for counseling and treatment. HIV care and treatment will take place at multiple local centers offering these services.

Interventions

BEHAVIORALAssisted Partner Services

Contact tracing for sexual and drug-sharing partners to notify about exposure to HIV and offer HIV and hepatitis C testing with linkage to care and partner services for those who test positive.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Kenyatta National Hospital
CollaboratorOTHER_GOV
Kenya Ministry of Health
CollaboratorOTHER_GOV
University of KwaZulu
CollaboratorOTHER
University of Washington
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

Prospective cohort study with nested cross-sectional studies

Eligibility

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

Inclusion criteria

* \> or = 18 years of age * Active intravenous drug use (IDU) as defined by injecting at least twice in the past month * Willing and able to provide informed consent * HIV infected (either new diagnosis or known diagnosis) * Willing and able to provide locator information for sexual and/or injecting partners

Exclusion criteria

• Classified as at high risk for IPV\* \*Participants will be classified as at moderate risk for IPV if they report 1) history of IPV during their lifetime either from a current or past partner; and/or 2) fear of IPV if they participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Sexual partners tested4 yearsNumbers of sexual partners tested for HIV and HCV per index participant
Injecting partners tested4 yearsNumbers of injecting partners tested for HIV and HCV per index participant
Partners diagnosed with HIV and HCV4 yearsNumber of partners newly diagnosed with HIV and HCV infection per index case
HIV-infected partners linked to HIV care4 yearsPercentage of HIV-infected partners linked to HIV care
HCV-infected partners linked to HCV care4 yearsPercentage of HCV-infected partners linked to HCV care
Index participants linked to HIV and HCV care4 yearsPercentage of index participants linked to HIV and HCV care

Countries

Kenya

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026