Development of Educational Intervention Through Technological Platform to Support Exclusive Breastfeeding up to Six Months Pilot Study
Mobile health app
Behavior
+ Breast Feeding
+ Feeding Behavior
Supportive Care Study
Summary
Study start date: August 15, 2024
Actual date on which the first participant was enrolled.This study focuses on creating a technological platform, specifically a mobile app, to support mothers in exclusively breastfeeding their babies for the first six months. This period is critical for an infant's health, as exclusive breastfeeding provides essential nutrients and strengthens the baby's immune system. By using a user-centered design approach, the study aims to develop an app that is both effective and user-friendly, incorporating feedback from mothers and experts. The educational content within the app is crafted with the help of breastfeeding specialists to ensure it is accurate and helpful, addressing a significant need for support during early motherhood. Participants in the study engage with the breastfeeding app, which is continuously refined based on user feedback and expert input. The app serves as a digital guide, offering educational materials and practical tips on breastfeeding. As part of the study, data is managed through a sophisticated system that tracks user interactions and outcomes, allowing researchers to analyze how the app impacts breastfeeding practices. The aim is to ensure the app effectively supports mothers, potentially leading to better health outcomes for both mothers and their babies.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.10 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 45 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives