Overview
Background: The transition to parenthood is stressful for first-time mothers and fathers and links to adverse health outcomes. Despite Internet use's popularity, an effective web-based, individually-tailored intervention to enhance parental self-efficacy and infant health for first-time parents remains lacking.
Objectives: This study aims to develop and evaluate the effectiveness of a web-based, individually-tailored childbirth and parenting intervention program on parenting self-efficacy and infant health outcomes. The feasibility and acceptability of a theory-driven intervention will be examined in first-time mothers and fathers.
Methods: A two-arm, single-blind randomized controlled trial will be conducted to investigate the effects of web-based intervention in the first-time mother and father. Participants will be randomly allocated to a web-based intervention or a control condition. A repeated measurement will be performed.
Anticipatory results: The efficacy of a theory-driven web-based, individually tailored intervention program will provide a valuable contribution to perinatal health care for first-time mothers and fathers.
Description
The primary outcome of parenting self-efficacy and breastfeeding self-efficacy. The secondary outcomes of anxiety, depression, sleep quality, social support, infant health outcomes will be assessed. Data will be analyzed with the intention-to-treat analysis using linear mixed-effects modeling.
Eligibility
Inclusion Criteria: for this study are first-time mothers and fathers who are
- 20 years old and above;
- primipara with a singleton pregnancy at second and third-trimester gestation;
- able to read and write in Mandarin;
- the husband or support partner will be willing to attend the intervention program;
- able to access and use the Internet by computer and/or smartphone daily.
Exclusion Criteria: are the first-time mothers and fathers who have
- chronic diseases;
- obstetric complications;
- an abnormal fetal screening;
- unable or unwilling to comply with the requirements of the research protocol;
- women and their partners did not have time for the web-based intervention program;
- participation on any other interventional study.