Microbicide/PrEP Acceptability Among Mothers and Male Partners in Africa (MAMMA)

Microbicide Trials Network

Status: Completed

Conditions: HIV Prevention

Treatments: Behavioral: In-depth Interview (IDI); Behavioral: Focus Group Discussion (FGD)

Study type: Observational

Funder types: NETWORK; NIH

Identifiers

NCT03648931

MTN-041

UM1AI106707 (U.S. NIH Grant/Contract)

38161 (Other Identifier)

UM1AI068633 (U.S. NIH Grant/Contract)

UM1AI068615 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The MTN-041 study is a multi-site exploratory study using focus group discussions (FGDs) and in-depth interviews (IDIs) to identify individual, interpersonal, social and cultural factors that may affect potential uptake of two safe and effective HIV prevention products, the monthly dapivirine (DPV) vaginal ring (VR) and daily oral pre-exposure prophylaxis (PrEP), by pregnant and breastfeeding women in Africa.

Full description

MTN-041 is an exploratory study primarily designed to identify individual, interpersonal, social and cultural factors that may affect potential uptake of two safe and effective HIV prevention products, the monthly DPV VR and daily oral PrEP, in a vulnerable yet seldom-studied population, pregnant and breastfeeding women. MTN-041 will utilize FGDs and IDIs to elicit community and health professional perceptions about vaginal practices, sexual activity, use of medicines, and HIV risk during pregnancy or breastfeeding, including how these perceptions may affect pregnant and breastfeeding women's acceptability of using intravaginal products and oral medications like the DPV VR and Truvada oral tablet.

The MTN-041 study population will consist of HIV-uninfected women 18-40 years old who are currently or were recently (within two years) pregnant or breastfeeding, men aged 18 years or older whose partners are currently or were recently (within two years) pregnant or breastfeeding, grandmothers whose daughters or daughters-in-law are currently or were recently (within two years) pregnant or breastfeeding, and key informants (KIs), which include: health care professionals (HCPs), traditional birth attendants (TBAs), providers of family planning, antenatal, and traditional health services to women, providers of other social services to women, and community leaders.

Up to 60 men and women will be selected at each site for participation in this study, for a maximum total of 240 study participants. This includes up to 50 FGD participants (currently or recently pregnant or breastfeeding women, male partners of women who are currently or were recently pregnant or breastfeeding, and grandmothers with currently or recently pregnant or breastfeeding daughters/daughters-in-law) and up to 10 KIs selected at each site, for a maximum total of 200 FGD participants and 40 KIs enrolled across all sites.

Enrollment: 232 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Able and willing to provide written informed consent in one of the study languages.

2. Able and willing to complete the required study procedures.

   For currently or recently pregnant or breastfeeding women:

3. Between the ages of 18 to 40 years old (inclusive) at Enrolment, verified per site standard operating procedures (SOPs).

4. Currently or recently (within two years) pregnant or breastfeeding (by self-report).

   For male partners:

5. Aged 18 years or older at Enrolment, verified per site SOPs.

6. Identifies as a primary sexual partner of a woman who is currently or was recently (within two years) pregnant or breastfeeding.

   For grandmothers:

7. Aged 18 years or older at Enrolment, verified per site SOPs.

8. Identifies as the maternal or paternal grandmother of a daughter or daughter-in-law who is currently or was recently (within two years) pregnant or breastfeeding.

   Note: The term "daughter-in-law" includes women who are/were not married to their male partner during or after pregnancy.

   For service provider KIs:

9. Aged 18 years or older at Enrolment, verified per site SOPs.

10. Currently working as a clinician (e.g., obstetrician, nurse, pharmacist, etc.), traditional care provider (e.g., TBA, healer, midwife, etc.), social service provider (e.g., social worker, family planning counselor, etc.) or community health worker in one of the study countries, verified per site SOPs.

11. Experienced in providing services to pregnant and/or breastfeeding women.

    For community leader KIs:

12. Aged 18 years or older at Enrolment, verified per site SOPs.

13. Currently acting in a community leadership role (e.g., local chief, religious leader, etc.).

Exclusion criteria

1. Has any condition that, in the opinion of the Investigator of Record (IoR)/designee, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives.
2. For currently or recently pregnant or breastfeeding women: known HIV-positive status, verified per recent health record (e.g., health passport, ante-natal book, HIV test card, or similar document) or by self-report if health record(s) not available.

Trial design

232 participants in 4 patient groups

Pregnant or Breastfeeding Women

Description:

No actual intervention is planned. A single focus group discussion (FGD) with community members in the same group assignment will be conducted to assess study outcome measures.

Treatment:

Behavioral: Focus Group Discussion (FGD)

Male Partners

Description:

No actual intervention is planned. A single focus group discussion (FGD) with community members in the same group assignment will be conducted to assess study outcome measures.

Treatment:

Behavioral: Focus Group Discussion (FGD)

Grandmothers

Description:

No actual intervention is planned. A single focus group discussion (FGD) with community members in the same group assignment will be conducted to assess study outcome measures.

Treatment:

Behavioral: Focus Group Discussion (FGD)

Key Informants

Description:

No actual intervention is planned. A single in-depth interview (IDI) will be conducted to assess study outcome measures.

Treatment:

Behavioral: In-depth Interview (IDI)