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Promoting Male Involvement to Improve PMTCT Uptake and Reduce Antenatal HIV Infection [retrospectively registered]

Promoting Male Involvement to Improve PMTCT Uptake and Reduce Antenatal HIV Infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201109000318329
Enrollment
480
Registered
2011-09-24
Start date
2010-12-06
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV/AIDS Pregnancy and Childbirth

Interventions

PartnerPlus: Couple risk reduction intervention

Sponsors

Human Sciences Research Council
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Eligible participants will be male and female. Women: a) pregnant women age 18 and older who have received HCT at the ANC, b) willing to attend PartnerPlus or PMTCT visits with their male partners, c) male partners must also be available to participate and d) both partners must be willing to participate in the study. Men: a) men aged 18 and older who are partners of pregnant women enrolled in the study, b) willing to attend PartnerPlus or PMTCT visits with their female partners, c) female partners must also be enrolled in the study and available to participate. All participants will be current adult residents of Mpumalanga Province and agree to attend four group sessions, 2 psychosocial assessments and 1 three day post-delivery assessment (maternal and infant only - blood sample assessment).

Exclusion criteria

Exclusion criteria: Exclusion Criteria: Women who are not currently pregnant or are unwilling to receive HCT are not eligible for this study. Women whose partners are not willing to participate are not eligible for this study. Men whose pregnant partners are unwilling to participate are not eligible for this study. Women and men who are not couples are not eligible to participate. Participants unable to provide informed consent will not be eligible.

Design outcomes

Primary

MeasureTime frame
1) increasing male partner participation in the PMTCT process, 2) increasing male HCT, 3) increasing maternal and infant adherence to the overall PMTCT protocol,

Secondary

MeasureTime frame
increasing the use of sexual barriers and reducing HIV transmission to mothers during pregnancy.

Countries

South Africa

Contacts

Public ContactKarl Peltzer

Research Director/HSRC

kpeltzer@hsrc.ac.za012-3022000

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026