Effectiveness of an Educational Intervention to Maintain Exclusive Breastfeeding (PROLACT)
Recruitment status was: Recruiting
|Exclusive Breastfeeding||Behavioral: Intervention group Behavioral: Usual care|
|Study Design:||Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
|Official Title:||Effectiveness of an Educational Group Intervention in Primary Care to Maintain Exclusive Breastfeeding. Cluster Randomised Clinical Trial. PROLACT Study.|
- Exclusive breastfeeding(EBF) [ Time Frame: six months ]Evaluate the presence of EBF 6 months after educational intervention.
- Type of breastfeeding, duration of EBF, reasons for breastfeeding ceasing intervention satisfaction (SERVQUAL). [ Time Frame: Six months ]
|Study Start Date:||February 2015|
|Estimated Study Completion Date:||December 2015|
|Estimated Primary Completion Date:||December 2015 (Final data collection date for primary outcome measure)|
Experimental: intervention group
Intervention group receive a training education on breastfeeding. Education training is provided by an expert group from General Direction of Primary Care
Behavioral: Intervention group
Education on breastfeeding
Behavioral: Usual care
Objective: Evaluate the effectiveness of an educational group intervention performed by primary healthcare professionals in terms of increasing the proportion of mother-infant pairs using exclusive breastfeeding at six months compared to routine practice. Design: cluster randomized trial. Setting: Multicentre. Primary Care Health Centres (PCHC). Madrid. Subjects: mother-infant pairs using exclusive breastfeeding who come for any query to the health centre, as long as the infant is not older than four weeks and who consent to participate in the study.
Sample size: N= 432 (216 in each arm). Randomisation: Unit of randomization: primary healthcare centres.
Analysis unit: mother-infant pairs, recruitment to consecutive sampling. Intervention: Educational group intervention in the treatment group and the usual intervention in the control group.
Variables: Main response variable: mother-infant pairs using exclusive breastfeeding (EBF) at six months. Secondary variables: type of breastfeeding at 6 months, duration of EBF, reasons for ceasing breastfeeding, satisfaction with the intervention (SERVQUAL). Prognostic variables: infant, mother and professional.
Data Analysis: Analysis of main effectiveness by intention to treat, comparing the proportion of mother-infant pairs using EBF at six months in both groups. The estimation adjusted using an explanatory logistics regression model. To assess the effect of the educational group intervention on the duration of the various type of breastfeeding, a survival analysis will be used comparing the two groups using the log-rank test. The control of potential confounding variables will be performed by the construction of various Cox regression models.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01869920
|Gerencia de Atencion Primaria||Recruiting|
|Contact: Susana Martín, Nurse firstname.lastname@example.org|
|Principal Investigator:||María J Santamaría, Nurse||Gerencia de Atención Primaria, Madrid|
|Principal Investigator:||Susana Martín, Nurse||Gerencia de Atención Primaria, Madrid|