Skip to main content
Clinical Trials/NCT03973476
NCT03973476CompletedNot Applicable

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

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina0 sites220 target enrollmentStarted: January 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
220
Primary Endpoint
Percentage of participants who breast-feed at 3 months of intervention

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Intervention group

Experimental

Mothers received a phone support service with their midwife during the 8 weeks after childbirth.

Intervention: Phone care support by midwife (Other)

Control group

No Intervention

Mothers received standard postpartum care

Outcomes

Primary Outcomes

Percentage of participants who breast-feed at 3 months of intervention

Time Frame: 3 months

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Sponsor Class
Other
Responsible Party
Sponsor

Similar Trials