Effect of Breastfeeding Optimization on Early Vascular Development

NCT01566812 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2017-03-07

No results posted yet for this study

Summary

This study aims to find out whether breast feeding optimization will increase breast feeding rates and to evaluate its effect on cardiovascular risk and general health of children.

Conditions

Interventions

BEHAVIORAL

Breast feeding optimization

Breast feeding optimization program extends from late pregnancy period to 6 months after birth. Prenatal intervention consists of individual and group counseling/education; perinatal intervention consists of in-hospital lactation support; postnatal intervention consists of home visit, counseling session, reminding telephone call and bulk SMS, special counseling for working mothers, breast pump rental, occupational-related support

BEHAVIORAL

Usual care

Usual care applied in the hospital

Sponsors & Collaborators

  • CEEBM

    collaborator UNKNOWN
  • Julius Center

    collaborator OTHER
  • Budi Kemuliaan Hospital

    collaborator UNKNOWN
  • Indonesia University

    lead OTHER

Principal Investigators

  • Nikmah S Idris, MD · Indonesia University

  • Cuno SPM Uiterwaal, Ass Prof, MD, PhD · Julius Center

  • Sudigdo Sastroasmoro, Prof, MD, PhD · CEEBM, University of Indonesia

  • Rulina Suradi, MD, Prof. · Indonesia University

  • Diederick E Grobbee, Prof, MD, PhD · Julius Center

  • Mohammad Baharuddin, MD · Budi Kemuliaan Hospital

  • Debby Bogaert, MD, PhD · Utrecht University

  • Annemieke MV Evelein, MD · Julius Center

  • Wahyuni Indawati, MD · Indonesia University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2018-02-28
Completion
2018-02-28

Countries

  • Indonesia

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01566812 on ClinicalTrials.gov