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Completed

NCT Number: NCT03235518

A Combination HIV Prevention Strategy for Young Women at Risk for HIV

The purpose of this study is to conduct formative research to inform the design and implementation of combination prevention interventions, including pre-exposure prophylaxis (PrEP) for female sex workers (FSW), as well as to inform recruitment and retention strategies for female sex workers and their male clients in Kenya.

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Key information

About this study

Despite remarkable advances in the global HIV response with 17 million persons, out of nearly 37 million living with HIV, who have initiated antiretroviral therapy (ART) in low- and middle-income countries (LMIC) as of end of 2015, there were an estimated 5,700 new HIV infections each day and a total of 2.1 million new HIV infections in 2015, of which 66% were in sub-Saharan Africa (SSA). Key populations within the generalized HIV epidemics in SSA, including female sex workers (FSW), have received insufficient attention, with data indicating that they are at disproportionate risk with limited access to prevention and treatment services. Globally, new infections among key populations and their sexual partners accounted for 36% of all new HIV infections in 2015. HIV prevalence among FSW is 29.3% worldwide. While reliable HIV prevalence estimates are lacking, younger FSW <25 years may be at significantly greater risk due to the confluence of biological, behavioral and structural risk factors.6 Mathematical modeling suggests that the proportion of new HIV infections attributable to sex work is likely to increase over time.

In settings where key populations contribute substantially to HIV burden, as in Kenya, effective integrated prevention strategies are urgently needed for populations such as FSW and can have a substantial impact on reducing new HIV infections.

In 2012, HIV prevalence among Kenyan 15-64 year olds was 5.6%, with 1,192,000 people living with HIV, but was markedly higher (15.1%) in the region of Kenya, formerly named Nyanza Province. HIV prevalence is 14.1% among FSW and 7.6% among male clients of sex workers (MC). FSW contribute significantly to new HIV infections in Kenya,14 with modelled estimates showing that 1 in 3 new HIV infections can be attributed to key populations.

Who can participate

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

Inclusion criteria

FSW. Inclusion criteria for the structured interviews, FGDs and IDI are identical.

  • Report being female or transgender women born make who have sex with men
  • Report being HIV-negative or unknown status
  • Report being between 18-24 years of age
  • Report residing or working in study community
  • Reports exchange sex for goods, money, flavors or other services in past 3 months
  • Willing to allow audio-recording of FGDs or IDI
  • Able to complete study procedures in English, Kiswahili or Dhuluo

Male Clients

  • Male
  • Report being >=18 years of age
  • Report exchanging goods, money, favors or other services for sex in past 3 months
  • Willing to allow audio-recording of IDI
  • Able to complete study procedures in English, Kiswahili or Dhuluo

Health Care Providers

  • Currently working as nurse or clinical officer at a clinic or other facility likely to offer PrEP
  • Report being >= 18 years of age
  • Willing to allow audio-recording of IDI
  • Able to complete study procedures in English

Exclusion criteria

  • Individuals who do not meet the inclusion criteria
  • Individuals who in the opinion of the investigators would interfere with adherence to study study requirements
  • FSW participating in FGD are not eligible for participation in IDI

Treatment and study plan

Primary outcomes

  1. Percentage of FSW participants who would be willing to participate in HIV prevention research

    Time frame: 6 months

    To inform prevention interventions for FSW, we will assess the percentage of FSW willing to participate in HIV prevention research or a PrEP study

Secondary outcomes

  1. Percentage of MC participants who would be willing to participate in HIV prevention research

    Time frame: 6 months

    To inform prevention interventions, we will assess the percentage of MC willing to participate in HIV prevention research

Sponsors and collaborators

Lead sponsor

Columbia University

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Acronym: IPrEP

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Aug 1, 2017
Registry last updated
Jan 10, 2022

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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