Web-based program to support first-time parents
The Development and Evaluation of a Web-based Childbirth and Parenting Intervention Program: A Randomized Controlled Trial
This study tests a web-based program designed to help first-time parents feel more confident and improve their baby's health by providing support and resources.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 600 (estimated) |
| Ages | 20 Years to 60 Years |
| Sex | All |
| Sponsor | Taipei Medical University Academic / other |
| Locations | 1 site (Taipei) |
| Trial ID | NCT04981730 on ClinicalTrials.gov |
What this trial studies
This study develops and evaluates a web-based intervention aimed at enhancing parenting self-efficacy and improving infant health outcomes for first-time mothers and fathers. It employs a two-arm, single-blind randomized controlled trial design, where participants are randomly assigned to either the intervention group or a control group. The program focuses on addressing psychological distress and promoting effective parenting strategies through tailored online resources. Outcomes such as anxiety, depression, sleep quality, and social support will also be assessed alongside primary outcomes related to parenting self-efficacy.
Who should consider this trial
Good fit: Ideal candidates for this study are first-time mothers and fathers aged 20 and above, who are in their second or third trimester of a singleton pregnancy and can read and write in Mandarin.
Not a fit: Patients with chronic diseases, obstetric complications, or those unable to comply with the study requirements may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this program could significantly improve the confidence and mental well-being of first-time parents, leading to better health outcomes for both parents and infants.
How similar studies have performed: Other studies have shown success with web-based interventions for parenting support, indicating potential for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: for this study are first-time mothers and fathers who are 1. 20 years old and above; 2. primipara with a singleton pregnancy at second and third-trimester gestation; 3. able to read and write in Mandarin; 4. the husband or support partner will be willing to attend the intervention program; 5. able to access and use the Internet by computer and/or smartphone daily. Exclusion Criteria: are the first-time mothers and fathers who have 1. chronic diseases; 2. obstetric complications; 3. an abnormal fetal screening; 4. unable or unwilling to comply with the requirements of the research protocol; 5. women and their partners did not have time for the web-based intervention program; 6. participation on any other interventional study.
Where this trial is running
Taipei
- Taipei Medical University Hospital — Taipei, Taiwan (Recruiting)
Study contacts
- Principal investigator: Shu-Yu Kuo — Taipei Medical University
- Study coordinator: Shu-Yu Kuo
- Email: sykuo@tmu.edu.tw
- Phone: +886-2-2736-1661
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.