CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 162 enrolled
Drug / intervention
Programme to Support Breastfeedingother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06653595
NCT06653595N/ACompleted
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Randomized Control Trial to Evaluate a Breastfeeding Support and Promotion Program to Improve the Health of Premature Babies (PAP-LM)

University of Barcelona·interventional·Posted Oct 22, 2024·Updated Oct 22, 2024

In Brief

A clinical study evaluating Programme to Support Breastfeeding for Prematurity; Extreme and Prematurity. Completed, enrolled 162 participants across 2 sites.

Detailed Summary

This study evaluates the effectiveness of a breastfeeding support and promotion program to increase exclusive breastfeeding rates in the preterm group. The intervention is performed by an Advanced Practice Nurse and International Board Certified Breastfeeding Consultant (IBCLC), with high expertise in breastfeeding problems. It is a combination of face-to-face, home care and telephone attention to improve the adherence to breastfeeding. The intervention lasts 6 months.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPrematurity; Extreme, Prematurity
CountriesSpain
Collaborators--

Timeline

N/ACompletedFinished
20222023202420252026
First PostedOct 22, 2024
Enrollment StartOct 13, 2021
Primary CompletionFeb 15, 2024
Study CompletionMar 20, 2024
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 1.7 years ago

Interventions

Programme to Support Breastfeedingother

The intervention consists of active support for breastfeeding by a lactation expert and IBCLC until the premature baby is 6 months old. The intervention includes: 1 face-to-face pre-discharge session, 8 home sessions up to 4 months and 3 telephone sessions up to 6 months.