Healthy Beginning Initiative (HBI)
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|ClinicalTrials.gov Identifier: NCT01795261|
Recruitment Status : Unknown
Verified November 2015 by University of Nevada, Reno.
Recruitment status was: Active, not recruiting
First Posted : February 20, 2013
Last Update Posted : December 2, 2015
|Condition or disease|
|Study Type :||Observational|
|Estimated Enrollment :||5400 participants|
|Observational Model:||Case Control|
|Official Title:||Comparative Effectiveness of Congregation and Clinic Based Approaches to Prevention of Mother to Child Transmission of HIV|
|Study Start Date :||September 2012|
|Estimated Primary Completion Date :||September 2016|
|Estimated Study Completion Date :||September 2016|
Prevention of mother to child transmission of HIV
Lifestyle counseling Male
male partners and PMTCT completion rate among HIV-infected pregnant women.
- Analysis of HIV testing rates in pregnant women and their male partners in a congregation based approach compared to a health facility based approach. [ Time Frame: One year ]We need to have 1,313 pregnant women in each arm of the study and follow them through pregnancy and up to 6 weeks post-delivery. Since pregnant women will be recruited at different stages of pregnancy, we will need to end recruitment 5 months after the study is open to recruitment and allow time to follow last recruited pregnant women through 9 months of pregnancy and up to 6 weeks post-delivery (approximately 11 months).
- Associations between HIV Test and Interventions and other covariates (risk factors) at individual- and community (church)-level will also be analyzed. [ Time Frame: one year ]Variables include age, household income, education level, previous HIV testing, last menstrual period, marital status, and employment status. HIV testing and PMTCT completion: will be assessed using a one-page investigator-administered questionnaire completed by pregnant women during the baby reception.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01795261
|PeTR Global Solutions|
|Abuja, Maitama, Nigeria|
|Principal Investigator:||Echezona Ezeanolue, MD||University of Nevada, Reno|