Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
FEMALE
ID06157697

Social Transfers for Exclusive Breastfeeding in São Paulo, Brazil

Led by Swiss Tropical & Public Health Institute · Updated on 2025-06-24

400

Participants Needed

2

Research Sites

95 weeks

Total Duration

On this page

Sponsors

S

Swiss Tropical & Public Health Institute

Lead Sponsor

U

University of Sao Paulo

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the impact of social transfers on exclusive breastfeeding rates in São Paulo, Brazil. The study aims to find out if providing social transfers can increase exclusive breastfeeding rates, extend the duration of exclusive and complementary breastfeeding, and improve long-term child health and development. Participants are mothers who have recently given birth and are breastfeeding exclusively. Participants are randomly assigned to one of three groups: a control group receiving only educational materials about breastfeeding benefits and recommendations; a non-conditional social transfer group receiving gifts at six months postpartum regardless of breastfeeding status; and a conditional social transfer group receiving gifts only if they are still exclusively breastfeeding at six months. Gifts include options such as diapers, hygiene products, toys, or transport vouchers. Throughout the study, researchers will compare breastfeeding rates and durations at six months postpartum among groups. Child health and early development will be assessed at 1 month, 6 months, 1 year, and 2 years. Mothers will receive education about breastfeeding benefits at baseline. The study will track exclusive and complementary breastfeeding patterns as well as child developmental outcomes over two years.

CONDITIONS

Brief Title

Social Transfers for Exclusive Breastfeeding in Brazil

Who Can Participate

Age: 18Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Gave birth in the last 72 hours
  • Exclusively breastfeeding at time of recruitment and intend to continue to exclusively breastfeed
  • Part of or eligible Bolsa Familia or on the Bolsa Familia list (CAD Unico)
  • Lives in São Paulo
  • No illnesses that contraindicates breastfeeding
  • Had a healthy singleton infant of 37 weeks or more gestation with a birth weight of at least 2500 grams
  • Agrees to participate and sign an informed consent; if under age (12-17 years), a legal representative will also have to agree to sign the informed consent
Not Eligible

You will not qualify if you...

  • Plans to move permanently outside study area
  • Has a medical, intellectual or psychological disability
  • Contraindication for breastfeeding
  • Preterm births
  • Children born with < 2500 grams

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 6 months postpartum

Participants receive educational materials about exclusive breastfeeding and may receive social transfer gifts at 6 months postpartum, depending on their group assignment.

Baseline visit and 6-month visit

Follow-up

Duration - Up to 2 years postpartum

Participants are followed up to assess child health and breastfeeding outcomes up to 2 years postpartum.

Visits at 1 month, 6 months, 1 year, and 2 years postpartum

Trial Site Locations

Total: 2 locations

1

University of Sao Paulo

São Paulo, Butantã, Brazil, 05508-220

Actively Recruiting

2

Federal University of São Paulo

São Paulo, Brazil, 04021-001

Actively Recruiting

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Research Team

J

Jordyn Wallenborn

S

Stephanie Khoury

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

3

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