Actively Recruiting
The Development and Evaluation of a Web-based Childbirth and Parenting Intervention Program
Led by Taipei Medical University · Updated on 2025-01-28
600
Participants Needed
1
Research Sites
95 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The Development and Evaluation of a Web-based Childbirth and Parenting Intervention Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
- Husband or support partner willing to attend the intervention program
- Able to access and use the Internet by computer and/or smartphone daily
You will not qualify if you...
- Having chronic diseases
- Having obstetric complications
- Having an abnormal fetal screening
- Unable or unwilling to comply with study requirements
- Women and partners without time for the web-based intervention
- Participation in any other interventional study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Taipei Medical University Hospital
Taipei, Taiwan, 110
Actively Recruiting
Research Team
S
Shu-Yu Kuo
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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