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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02106026
Other study ID # LACT-120413
Secondary ID
Status Completed
Phase N/A
First received March 28, 2014
Last updated April 2, 2014
Start date December 2004
Est. completion date October 2006

Study information

Verified date April 2014
Source Universidad Miguel Hernandez de Elche
Contact n/a
Is FDA regulated No
Health authority Argentina: Ministry of Health
Study type Interventional

Clinical Trial Summary

An antenatal education intervention in primiparous women improves breastfeeding duration and reduces post-natal complications.


Description:

A randomized controlled clinical trial of an educational intervention was undertaken at a public hospital. the investigators compared a health education based on techniques to prevent complications and increase information about the benefits of breastfeeding with the usual practice. A group of nurses delivered the educational intervention. The trial involved randomization of 314 primiparous women. The analysis was by 'intention-to-treat'.


Recruitment information / eligibility

Status Completed
Enrollment 314
Est. completion date October 2006
Est. primary completion date October 2006
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- primiparous women,

- no contraindications to breastfeeding,

- no skin disorders,

- no breast surgery,

- voluntary provision of data to enable their later localization.

Exclusion Criteria:

- women who planned to deliver their babies in other hospitals,

- twin pregnancy

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Intervention

Other:
Preventive education
The intervention group received education to facilitate successful breastfeeding and symptom management as nipple pain. This was supported by strategies designed to (1) prevent problems associated with breastfeeding (nipple lesions, cracks and mastitis), (2) perform breast-care procedures, (3) strengthen information about the advantages of maternal breastfeeding (nutritional support, importance as food for the baby, availability, post-partum recovery) and (4) provide asepsis and hygiene measures.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Universidad Miguel Hernandez de Elche

Outcome

Type Measure Description Time frame Safety issue
Primary Breastfeeding duration At 6 months postpartum No
Primary Breastfeeding duration At 1 month postpartum
Secondary Knowledge about breastfeeding and care of the breasts, Inmediate postpartum period. No
Secondary Incidence of mothers with post-natal breast complications, such as cracks, breast lesions or mastitis At 1 month postpartum No
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