Healthy women
Conditions
Interventions
Women in the control group will receive conventional breastfeeding support in the hospital and in the community.
Women in the intervention group will also receive conventional breastfeeding support.
Sponsors
Graduate School of Medicine, The University of Tokyo
Lao Tropical and Public Health Institute, Ministry of Health, Lao People'
s Domestic Republic
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Eligibility criteria include the ability to participate in Laotian, and having had a singleton birth.
Exclusion criteria
Exclusion criteria: If either the women or her infant has a medical condition that can interfere with breastfeeding, she will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Infant feeding status 6 weeks, 14 weeks, and 6 months postpartum | — |
Secondary
| Measure | Time frame |
|---|---|
| Breastfeeding self-efficacy 6 weeks and 14 weeks postpartum | — |
Countries
Asia(except Japan)
Contacts
Public ContactKeiko Nanishi
The University of Tokyo Graduate School of Medicine
Outcome results
None listed