Completed

Father-Involvement Breastfeeding Telephone Support for Exclusive Breastfeeding and Postnatal Care

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

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.

What is being tested

Breastfeeding telephone support

Behavioral
Who is being recruted

Behavior

+ Breast Feeding

+ Feeding Behavior

Over 18 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: April 2022
See protocol details

Summary

Principal SponsorThe Hong Kong Polytechnic University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleThe Effect of a Father-involvement Breastfeeding Telephone Support Intervention on Exclusive and Sustained Breastfeeding: A Randomized Controlled Trial.
NCT05109988
Principal SponsorThe Hong Kong Polytechnic University
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

649 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

BehaviorBreast FeedingFeeding Behavior

Criteria

3 inclusion criteria required to participate
giving birth to a single healthy baby at term

ability to speak and read the Chinese language

aged 18 years or above

1 exclusion criteria prevent from participating
psychiatric illness

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants in this group receive weekly, personalized breastfeeding counseling sessions over the phone. These sessions last between 20 to 30 minutes and are conducted in the first month after the baby's birth, for both mothers and fathers.

Study 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

Suspended

Ngai Fei Wan

Hong Kong, Hong KongOpen Ngai Fei Wan in Google Maps
CompletedOne Study Center