Adolescent Mothers, Grandmothers, Breastfeeding and Complementary Feeding

May 28, 2009 updated by: Hospital de Clinicas de Porto Alegre

Effect of Intervention About Breastfeeding and Complementary Feeding in Adolescent Mothers and Their Grandmothers

The purpose of this study is to determine whether counseling sessions on breastfeeding for adolescent mothers and their grandmothers in the maternity ward and at home are effective in to improve the exclusive and total breastfeeding rates during the first six month, as well as the convenient timing of supplementary feeding introduction.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Despite the recognized value of exclusive breastfeeding during the first months of a child's life and efforts for promoting this practice, rates for this pattern of breastfeeding in Brazil are below those recommended by the World Health Organization(WHO), which advocates exclusive breastfeeding during the first 6 months. The last national survey about the prevalence of breastfeeding revealed a median duration of 10 months. However , the length of exclusive breastfeeding was only 23 days.

A lot of studies identified maternal age as predictor of breastfeeding. In African, Asian, Latin American and the Pacific societies, older women, or grandmothers,traditionally have considerable influence on decisions related to maternal and child health at the household level.

Considering all that, interventions intended to increase frequency of breastfeeding, particularly exclusive breastfeeding. However, there are few studies on this subject.

Study Type

Interventional

Enrollment (Actual)

344

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Rio Grande do Sul
      • Porto Alegre, Rio Grande do Sul, Brazil, 90035-903
        • Hospital de Clínicas de Porto Alegre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Adolescent mothers
  • Mothers living in the city of Porto Alegre
  • Healthy nontwin newborns with birth weight equal or greater than 2500g

Exclusion Criteria:

  • Mothers living with mother-in-law
  • Mother-infant pairs that were unable to stay together due to a health concern in either the mother or infant
  • Mammaplasty reductive

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: visit with grandmother
Teenagers mothers and their grandmothers receive counseling sessions about breastfeeding and complementary feeding.
The intervention groups received counseling sessions about breastfeeding and complementary feeding at maternity ward and at home with 7,15,30,60 and 120 days.
Other Names:
  • Group one- no grandmother and no intervention
  • Group two- no gradmother and with intervention
  • Group three - with grandmother and no intervention
  • Group four- with grandmother and with intervention
Experimental: visit without grandmother
Teenagers mothers don´t live with their grandmothers and receive counseling sessions about breastfeeding and complementary feeding.
The intervention groups received counseling sessions about breastfeeding and complementary feeding at maternity ward and at home with 7,15,30,60 and 120 days.
Other Names:
  • Group one- no grandmother and no intervention
  • Group two- no gradmother and with intervention
  • Group three - with grandmother and no intervention
  • Group four- with grandmother and with intervention
No Intervention: no visit with grandmother
Teenagers mothers live with their grandmothers and don´t receive counseling sessions about breastfeeding and complementary feeding.
No Intervention: no visit without grandmother
Teenagers mothers don´t live with their grandmothers and don´t receive counseling sessions about breastfeeding and complementary feeding.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Frequency of exclusive and total breastfeeding
Time Frame: First year
First year

Secondary Outcome Measures

Outcome Measure
Time Frame
Pattern of complementary feeding
Time Frame: one year
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: ELSA REGINA J GIUGLIANI, MD,PhD,IBCLC, Hospital de Clínicas de Porto Alegre

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2006

Primary Completion (Actual)

August 1, 2008

Study Completion (Actual)

January 1, 2009

Study Registration Dates

First Submitted

May 28, 2009

First Submitted That Met QC Criteria

May 28, 2009

First Posted (Estimate)

May 29, 2009

Study Record Updates

Last Update Posted (Estimate)

May 29, 2009

Last Update Submitted That Met QC Criteria

May 28, 2009

Last Verified

May 1, 2009

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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