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Clinical Trials/NCT03357549
NCT03357549
Completed
N/A

Effectiveness of an Brief Motivational Intervention to Promote Breastfeeding

University of Extremadura1 site in 1 country88 target enrollmentJanuary 11, 2018
ConditionsBreast Feeding

Overview

Phase
N/A
Intervention
Not specified
Conditions
Breast Feeding
Sponsor
University of Extremadura
Enrollment
88
Locations
1
Primary Endpoint
Changes in degree of exclusivility of Breastfeeding
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Breastfeeding is the ideal feeding for the newborn. The success of the initiation and maintenance of breastfeeding can be influenced by different factors, as breastfeeding self-efficacy. Brief Motivational Intervention (BMI) is a form of collaborative guidance, person-centered approach aimed at strengthening the motivation to adopting healthy initiatives and can increase the self-efficacy.

The hypothesis is that an BMI to promote breastfeeding, during immediate postpartum plus telephone support at the first and third postpartum months, will significant increase in the adherence and duration of breastfeeding compared with the habitual education action applied at the same time. Also, the BMI will increase the breastfeeding self-efficacy of the particpants, and this breastfeeding self-efficacy will be a mediator of the effect between the IMB and the breastfeeding duration.

The general self-efficacy of the participants will change the size of the effect of BMI.

Registry
clinicaltrials.gov
Start Date
January 11, 2018
End Date
March 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University of Extremadura
Responsible Party
Principal Investigator
Principal Investigator

Cristina Franco Antonio

Nurse specialist in obstetrics and gynecology (Midwife)

University of Extremadura

Eligibility Criteria

Inclusion Criteria

  • All women with term gestations who have given birth healthy newborns by vaginal delivery at the hospital .who agree to participate in the study by signing informed consent, will be includes in the study

Exclusion Criteria

  • Mothers who, by medical indication or own decision, do not initiate breastfeeding in the first hour of the newborn's life.
  • Mother of children who require admission to the neonatal unit.
  • Women with a previously diagnosed psychiatric disorder.
  • Neurological or cognitive impairment that impedes the evaluation and the BMI
  • Resident status that prevents correct follow-up of patients (eg. residence outside Spain).
  • Women with language or communication barriers

Outcomes

Primary Outcomes

Changes in degree of exclusivility of Breastfeeding

Time Frame: 1st, 3st and 6th month postpartum

Breastfeeding is measure acording to degree of exclusivity, acording to WHO definition: Exclusive breastfeeding, Predominant breastfeeding and Partial breastfeeding

Secondary Outcomes

  • Changes in Breastfeeding Self-efficacy(Pre-intervention. 1st, 3rd and 6th month)
  • Changes on General Self-efficacy(Pre-intervention, 1st, 3rd and 6th month)

Study Sites (1)

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