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Completed

NCT Number: NCT00931216

Integration of HIV Care and Treatment Into Antenatal Care in Migori District, Kenya

This study seeks to determine the most effective way to reach and provide pregnant women with accessible, comprehensive, and high quality HIV care and treatment.

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Key information

About this study

This study uses a prospective cluster randomized design. Twelve clinics similar in size, population, and services in Migori district, Kenya that provide ANC have been randomly assigned to receive "integrated ANC, PMTCT & HIV services" (intervention arm) or "non-integrated services" (control arm). At the intervention clinics, pregnant women will receive ANC, PMTCT and HIV care and treatment (including HAART if required) at the same clinic visit from the ANC provider. At the control clinics, women will receive antenatal care and PMTCT services with referral to the HIV care and treatment department located in the same facility. The control sites more closely resemble the current approach followed for care and treatment of HIV-infected pregnant women in Kenya. The content of ANC, PMTCT, and HIV care will be the same in the two study arms and will follow current Kenyan national guidelines. The only difference between the two arms will be the provider/location of HIV care and treatment.

Outcomes will be compared for HIV-positive pregnant women who attend intervention versus control facilities. In addition we will conduct qualitative research with health care providers at the study health facilities in order to learn provider perspectives on the two service models and to explore the effects of integration on provider job satisfaction (including work load).

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • FOR SITE INCLUSION:
  • Each site must provide ANC services
  • Each site must provide HIV testing services for pregnant women
  • Each site must have an average of at least 20 new ANC clients per month
  • FOR ENROLLMENT OF HIV-POSITIVE WOMEN:
  • All women testing HIV-positive at one of the 12 ANC clinics included in the study will be asked to participate in the study
  • FOR HEALTH PROVIDER INCLUSION IN INTERVIEWS:
  • Health care staff must work within the ANC clinic at selected facilities
  • Staff must be able to read and speak English well enough to complete the informed consent process, participate in a one-on-one in-depth interview in English and complete a brief self-administered questionnaire

Exclusion criteria

  • FOR SITE EXCLUSION:
  • If all of inclusion criteria are not met the site will be excluded
  • If site is already providing integrated ANC/HIV care services
  • FOR HEALTH PROVIDER INCLUSION IN INTERVIEWS:
  • If all of inclusion criteria are not met the site will be excluded

Treatment and study plan

Integrated ANC, PMTCT, HIV services

Procedure

Of the 12 study clinics, 6 will be randomized to receive the intervention. At these 6 facilities, health care providers within the ANC department will be trained to also provide HIV/PMTCT care. Women testing positive within ANC clinics at integrated facilities will receive ANC, PMTCT and HIV services within the same visit/same service provider rather than being referred for HIV care and treatment.

Primary outcomes

  1. Vertical transmission of HIV

    Time frame: 3 months postpartum

Secondary outcomes

  1. Maternal HIV treatment outcomes

    Time frame: 6 months, 1 year

  2. Provider job satisfaction

    Time frame: 1 year

  3. Infant HIV testing uptake

    Time frame: 3 months postpartum

  4. Patient enrollment, retention and adherence in HIV care and treatment

    Time frame: 6 months, 1 year

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • Centers for Disease Control and Prevention
  • Kenya Medical Research Institute

Registry information

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Jul 2, 2009
Registry last updated
Apr 10, 2012

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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