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Completed

NCT Number: NCT01869920

Effectiveness of an Educational Intervention to Maintain Exclusive Breastfeeding

Hypothesis: An educational intervention increases the proportion of mother-infant pairs using exclusive breastfeeding

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Gerencia de Atencion Primaria

Madrid, Spain

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female 18 years old or older,
  • mother-infant pairs using exclusive breastfeeding,
  • Signed Informed Consent

Exclusion criteria

  • Any medical conditions that prevents breastfeeding
  • infant should be not older than four weeks

Treatment and study plan

Intervention Group

Behavioral

Education on breastfeeding

Usual Care

Behavioral

Usual care

Primary outcomes

  1. Exclusive breastfeeding (EBF)

    Time frame: six months

    Evaluate the presence of EBF 6 months after educational intervention.

Secondary outcomes

  1. Type of breastfeeding and duration of EBF

    Time frame: Six months

    EBF or not exclusive breastfeeding and duration in months

  2. breastfeeding ceasing

    Time frame: During follow-up

    Reasons for breastfeeding ceasing

Sponsors and collaborators

Lead sponsor

Gerencia de Atención Primaria, Madrid

Other Gov

Registry information

Official study title

Effectiveness of an Educational Group Intervention in Primary Care to Maintain Exclusive Breastfeeding. Cluster Randomised Clinical Trial. PROLACT Study.

Acronym: PROLACT

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Jun 5, 2013
Registry last updated
Aug 22, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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