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Effectiveness of Midwife Phone Support With the to Reduce the Early Abandonment of Breastfeeding

Not Applicable
Completed
Conditions
Breastfeeding
Interventions
Other: Phone care support by midwife
Registration Number
NCT03973476
Lead Sponsor
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Brief Summary

Objective: To evaluate the effectiveness of telephone support of the reference midwife, in relation to the abandonment of breastfeeding of primiparous mothers and to identify, both the risk factors and the protective factors for the early abandonment of breastfeeding.

Material and Method Randomized parallel controlled clinical trial.

Detailed Description

Sample: 220 primiparous mothers with access, during the 8 weeks postpartum, to a mobile phone to contact the midwife randomization of 110 mothers to the experimental group and 110 to the control group. The mothers of the experimental group will be offered the mobile phone number to contact their midwife after delivery. The mothers of the control group will receive the usual attention of the portfolio of services that includes the spontaneous visit in the center, the telephone call in the center, the home visit and the health education groups.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
220
Inclusion Criteria
  • Primiparians who carry out the follow-up of pregnancy for the midwife
  • The pregnant woman is of low risk
  • Possibility of the mother to make calls to the mobile phone.
  • The pregnant woman wishes to participate in the study.

Exclusion Criteria

  • Maternal or fetal pathology that can condition maternal breastfeeding.
  • idiomatic barrier.
  • Prematurity.
  • Baby with weight <2,500 gr. at birth
  • Home delivery during the puerperium
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupPhone care support by midwifeMothers received a phone support service with their midwife during the 8 weeks after childbirth.
Primary Outcome Measures
NameTimeMethod
Percentage of participants who breast-feed at 3 months of intervention3 months

Women who still breastfeed 3 months after the intervention with respect to the control arm

Secondary Outcome Measures
NameTimeMethod
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