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OpenTrials
Completed

NCT Number: NCT02556957

CHWs, mHealth, and Combination HIV Prevention

Kasensero, a fishing community on Lake Victoria in Uganda, is a representative HIV "hotspot" with extremely high HIV prevalence (44.3%) and incidence (~3.9/100py), yet low HIV service utilization. Hotspots such as Kasensero may seed and sustain HIV in general populations, compromising national and regional HIV control efforts. PEPFAR, UNAIDS, and WHO have recognized the urgent need to target hotspots with enhanced HIV treatment and prevention efforts. However, evidence on low-cost, comprehensive, and effective HIV control strategies for hotspots is limited and is thus a priority need for the field.

The investigators propose an implementation science, cluster-randomized, controlled trial in Kasensero to evaluate the impact on HIV service uptake and HIV incidence of CHWs promoting combination HIV prevention (CHP) services supported by mobile health technologies (mHealth). CHP is the implementation of multiple, evidence-based HIV prevention services (HIV testing and counseling, antiretroviral therapy, medical male circumcision, and behavior change) to maximize population-level impact on HIV incidence. For CHP to substantively decrease HIV incidence, most community members must be assessed for risk factors and current CHP utilization, then triaged, motivated, linked, and, if HIV-infected, retained in care. The proposed intervention will use low-cost CHWs leveraging mHealth decision support and counseling tools to promote CHP along this entire continuum of HIV service utilization. The hypotheses for this implementation science research are that residents in clusters receiving the implementation intervention will have improved CHP service uptake and decreased Population Prevalence of Viremia (PPDV) compared to controls receiving standard of care.

The intervention will be evaluated through a pragmatic, cluster-randomized trial nested within a large, ongoing population-based cohort study of HIV, the Rakai Community Cohort Study (RCCS). Intervention arm participants will be visited in their place of residence by CHWs trained to evaluate and triage participants into risk categories, provide tailored CHP health counseling, linkage, and adherence support, all supported by a mHealth decision support tool. The primary outcomes will be CHP service coverage and PPDV. Other outcomes will be HIV incidence, population viral load, implementation measures, retention, virologic suppression, and sexual behaviors.

Complimentary mixed methods (quantitative, qualitative, and cost) evaluations of the trial will be conducted to evaluate implementation processes, facilitators, and barriers to inform study results and future program uptake. Focus groups and in-depth interviews will be conducted during and after the follow-up period and synthesized with quantitative data. Intervention costs will be prospectively measured to provide information on program affordability.

Through this study, a novel, low-cost, and scalable implementation intervention to improve CHP uptake will be evaluated in an HIV "hotspot" critical to controlling the HIV epidemic. The study design ensures rigorous evidence of immediate relevance to many stakeholders.

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Key information

Conditions

HIV

Age range

15 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rakai Health Sciences Program

Entebee, Uganda

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Resident of Kasensero

Exclusion criteria

-

Treatment and study plan

HealthScouts

Behavioral

Standard of care

Other

Primary outcomes

  1. Population Prevalence of Detectable Viremia

    Time frame: 4 Years

    Proportion of the entire population who have detectable HIV viremia

  2. ART Coverage (self-report)

    Time frame: 4 Years

    Proportion of HIV+ persons who are on ART

  3. HIV Care Coverage (self-report)

    Time frame: 4 years

    Proportion of HIV+ persons who are in HIV care

  4. Medical Male Circumcision Coverage (self-report)

    Time frame: 4 years.

    Proportion of men who are circumcised

Secondary outcomes

  1. HIV Incidence

    Time frame: 4 years.

  2. Sexual Behaviors (self-report)

    Time frame: 4 years

    Proportion of the population which has multiple partners and/or inconsistent or no condom use

  3. Population HIV Viral Load

    Time frame: 4 years

    The mean viral load of HIV+ persons

  4. HIV Counseling and Testing Coverage (self-report)

    Time frame: 4 years

    Proportion of the entire population who have received HIV Counseling and Testing

  5. HIV Prevalence

    Time frame: 4 years

    The prevalence of HIV in the entire population

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Registry information

Official study title

CHWs, mHealth, and Combination HIV Prevention: An Implementation Science Cluster-Randomized Trial (mLAKE)

Acronym: mLAKE

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Sep 22, 2015
Registry last updated
Aug 31, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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