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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01494961
Other study ID # ANRS 12127 Prenahtest
Secondary ID
Status Completed
Phase N/A
First received December 15, 2011
Last updated December 16, 2011
Start date February 2009
Est. completion date October 2011

Study information

Verified date December 2011
Source French National Agency for Research on AIDS and Viral Hepatitis
Contact n/a
Is FDA regulated No
Health authority Cameroon: Ministry of Public HealthDominican Republic: Comité de Etica Indepediente, Fundacion Dominica de InsectoligiaGeorgia: Maternal and Child Care UnionIndia: Independent Ethics Committee for Prayas Health Group
Study type Interventional

Clinical Trial Summary

ANRS 12127 Prenahtest is an intervention trial conducted in four countries (Cameroon, Dominican Republic, Georgia and India), where pregnant women are randomized during prenatal care to receive either standard post-test HIV counseling, or an innovative intervention called couple-oriented post-test HIV counseling (COC).

The aim of the COC intervention is to empower women to communicate with her male partner about HIV, and HIV testing in particular, and encourage him to return for HIV testing and/or couple HIV counseling (where both couple members are counseled together).

Prenahtest is the first randomised trial testing a prenatal intervention to increase partner HIV testing.


Recruitment information / eligibility

Status Completed
Enrollment 1943
Est. completion date October 2011
Est. primary completion date August 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 15 Years and older
Eligibility Inclusion Criteria:

- Attending her first ANC visit for the current pregnancy in the study centre

- Accepting to participate in the study and being able to give informed consent ii

- Currently having a partner (the man who the woman considers as her regular partner on the day of inclusion, even if this person is not the baby's father) iii

- Accepting follow-up (including home visits if necessary) by the project staff until 15 months after delivery

Exclusion Criteria:

- Having been tested for HIV during her current pregnancy

- Having a male partner who was tested for HIV during her gestational period v

- Having a partner who works out of the predefined study area or is absent for more then 6 months

- Being unwilling/unable to provide address/contact information

- Having an intoxication and/or mental impairment at the moment of recruitment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Behavioral:
Couple-oriented post-test HIV counseling
COC is an individual behavioural intervention, strengthening standard post-test HIV counselling delivered to pregnant women after prenatal HIV testing. COC was based on the assumption that developing women's communication skills and self-efficacy during HIV counselling would enable them to discuss HIV and sexual issues with their partners, and yield tangible effects on partner HIV testing. The structure of the COC intervention was adapted from a WHO PMTCT counselling manual and was described in a COC manual, which was used to train the COC counsellors and could also be used during the counselling session. Tested during the pilot phase of the trial, COC was shown to be feasible and acceptable in the four study sites.

Locations

Country Name City State
Cameroon Centre Mère - Enfant Chantal Biya Yaoundé
Dominican Republic Hospital Materno-Infantil "San Lorenzo" de los Mina Santo Domingo
Georgia Maternity Hospital N°5 Tbilisi
India Sane Guruji Hospital Pune

Sponsors (2)

Lead Sponsor Collaborator
French National Agency for Research on AIDS and Viral Hepatitis Elizabeth Glaser Pediatric AIDS Foundation

Countries where clinical trial is conducted

Cameroon,  Dominican Republic,  Georgia,  India, 

References & Publications (2)

Orne-Gliemann J, Tchendjou PT, Miric M, Gadgil M, Butsashvili M, Eboko F, Perez-Then E, Darak S, Kulkarni S, Kamkamidze G, Balestre E, du Loû AD, Dabis F. Couple-oriented prenatal HIV counseling for HIV primary prevention: an acceptability study. BMC Publ — View Citation

Tchendjou PT, Koki PN, Eboko F, Malateste K, Essounga AN, Amassana D, Mossus T, Tejiokem M, Boisier P, Orne-Gliemann J. Factors associated with history of HIV testing among pregnant women and their partners in Cameroon: baseline data from a Behavioral Int — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Partner HIV testing Proportion of male partners tested for HIV during the study follow-up period (from post-test HIV counseling to the last follow-up visit at 6 months postpartum) among the pregnant women enrolled in the trial 6 months postpartum No
Secondary Couple HIV counseling Proportion of women receiving couple HIV counseling uring the study follow-up period (from post-test HIV counseling to the last follow-up visit at 6 months postpartum) among the pregnant women enrolled in the trial 6 months postpartum No
Secondary HIV incidence Proportion of women tested HIV-positive during the study follow-up period (from post-test HIV counseling to the last follow-up visit at 6 months postpartum) among the pregnant women tested HIV-negative at enrolment 6 months postpartum No
Secondary Couple communication of sexual and reproductive health Proportion of women reporting having discussed sexual and reproductive health issues (family planning, HIV, condom) during the study follow-up period (from post-test HIV counseling to the last follow-up visit at 6 months postpartum) among the pregnant women enrolled in the trial 6 months postpartum No