Breastfeeding Clinical Trial
Official title:
Ecological Momentary Breastfeeding Intervention to Improve Breastfeeding Outcomes: a Randomized Controlled Trial
During Chinese mothers' doing the month, they are often housebound and find it difficult to attend group support or seek help during the first month postpartum which is the critical period in sustaining exclusive breastfeeding and at high risk of weaning. This can adversely affect their general well-being, and are associated with stress, anxiety and postnatal depression. Thus, mothers have expressed the need for real-time, real world, personalized support that allow them to get immediate breastfeeding support, helps in overcoming the challenges and subsequently improve exclusive breastfeeding. The aim of the proposed study is to assess the effectiveness of an ecological momentary intervention (EMI)-based breastfeeding intervention in improving exclusive breastfeeding outcomes and to inform clinical practice and services for breastfeeding mothers in Hong Kong. Such interventions have been considered as a rising shift from traditional model of care towards an e-technology based health model that may improve exclusive breastfeeding duration globally.
Status | Not yet recruiting |
Enrollment | 518 |
Est. completion date | January 31, 2026 |
Est. primary completion date | January 31, 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - be primiparous mothers - have had a singleton pregnancy and live birth - have birthed a full-term infant (37-42 weeks gestation) - speak Cantonese - be a Hong Kong resident - have no serious medical or obstetrical complications and have not had their infant admitted to the neonatal intensive care unit (NICU) Exclusion Criteria: - is < 37 weeks gestation - has an Apgar score < 8 at five minutes - has a birthweight < 2500 grams - is born with any severe medical conditions or congenital malformations - is placed in the special care nursery for more than 48 hours after delivery - is placed in the intensive care nursery after delivery |
Country | Name | City | State |
---|---|---|---|
Hong Kong | Queen Elizabeth Hospital | Hong Kong | |
Hong Kong | Queen Mary Hospital | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of participants in each study groups exclusively breastfeeding | The number of participants who are exclusively breastfeeding at each time point. | At 1, 2, 3 and 6 months postpartum | |
Primary | Overall duration of any breastfeeding in each study groups | The number of participants who are any breastfeeding at each time point. | At 1, 2, 3 and 6 months postpartum | |
Secondary | Breastfeeding self-efficacy scores between the two study groups | Breastfeeding efficacy measured using Breastfeeding Self-Efficacy Scale - Short Form (BSES-SF). BSES-SF is a 14-item scale with total score ranging from 14 to 70. A higher score indicates higher breastfeeding self-efficacy. | baseline and 1 and 3 months postpartum | |
Secondary | Infant feeding knowledge and attitude scores between the two study groups | Attitude towards breastfeeding measured using the Iowa Infant Feeding Attitude Scale (IIFAS). IIFAS is a 17-item scale with total score ranging from 17 to 85. A higher score indicates a more favorable attitude towards breastfeeding. | baseline and 1 and 3 months postpartum |
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