Effect of a Self-Efficacy-Based Educational Intervention on Breastfeending in Primigravid Women: A Randomized Controlled Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorInstituto Mexicano del Seguro Social

About this trial

This randomized controlled trial aims to evaluate the effect of a self-efficacy-based educational intervention on exclusive breastfeeding among primigravid women attending a primary care center in Mexico. Participants in the intervention group will receive four weekly educational sessions focused on breastfeeding knowledge, self-efficacy, problem-solving skills, and emotional support during the third trimester of pregnancy. The control group will receive standard prenatal care. Breastfeeding self-efficacy and exclusive breastfeeding rates will be evaluated during postpartum follow-up at 1 and 3 months after delivery.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Pregnant women aged 18 years or older

Primigravidae in the third trimester of pregnancy

Receiving prenatal care at UMF No. 9, IMSS

Ability to attend the educational sessions

Disqualifiers

High-risk pregnancy

Medical conditions contraindicating breastfeeding

Cognitive impairment or communication difficulties preventing participation

Previous participation in breastfeeding educational programs

Trial design

Design model

Parallel

Treatments tested in this trial

  • Breastfeeding Self-Efficacy Educational Program

    Behavioral

    Participants will receive four weekly educational sessions during the third trimester of pregnancy based on breastfeeding self-efficacy theory. Sessions will include breastfeeding education, practical techniques, confidence building, problem-solving strategies, and support to improve exclusive breastfeeding practices postpartum.

Treatment groups

160 Participants
are divided into 2 treatment groups
Group A: Educational Intervention GroupExperimental treatment 1 intervention
Group B: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Exclusive Breastfeeding Rate at 3 Months Postpartum

Proportion of mothers who maintain exclusive breastfeeding at 3 months postpartum after receiving an educational intervention based on breastfeeding self-efficacy.

Time frame
3 months postpartum

Secondary outcomes

Other outcomes

Sponsors and contacts

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Instituto Mexicano del Seguro Social

Lead sponsor

Tropical Disease Research Centre

Collaborator

This trial is not recruiting at the moment. You can still explore other options: