Father-Involvement Breastfeeding Telephone Support for Exclusive Breastfeeding and Postnatal Care
This study aims to support postnatal care by evaluating the impact of father-involvement breastfeeding telephone support on the prevalence of exclusive breastfeeding in infants younger than 1 month.
Breastfeeding telephone support
Behavior
+ Breast Feeding
+ Feeding Behavior
Supportive Care Study
Summary
Study start date: April 18, 2022
Actual date on which the first participant was enrolled.This study focuses on the benefits of exclusive breastfeeding for infants during their first six months of life, which includes protection against various illnesses and reduced risk of mortality and morbidity. The study aims to implement and evaluate the effectiveness of a breastfeeding telephone support intervention that involves both mothers and fathers during the postpartum period. The main goals are to assess the impact of this father-involvement intervention on the prevalence and duration of exclusive breastfeeding, postnatal depression, and parent-infant bonding. In this randomized controlled trial, a group of postpartum mothers and fathers will be assigned to either the experimental group, receiving the father-involvement telephone support intervention, or the control group, receiving standard postpartum care. The intervention consists of four weekly 20-30 minute telephone-administered counseling sessions on breastfeeding for mothers and fathers during the first month postpartum. The main outcome measures include the prevalence and duration of exclusive breastfeeding at 1, 2, 4, and 6 months postpartum, as well as postnatal depression and parent-infant bonding assessed using the Edinburgh Postnatal Depression Scale (EPDS) and Postpartum Bonding Questionnaire (PBQ) at 2 and 6 months postpartum. The results of this study may help policy makers and health professionals design better health promotion programs for breastfeeding families, potentially reducing the public health burden of childhood illness.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.649 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.Any sex
Biological sex of participants that are eligible to enroll.Over 18 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
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location