Using experiential classrooms to promote healthy behaviors during pregnancy
The Effect of Experiential Classroom on Establishing Healthy Behaviors During Pregnancy
This study tests if a hands-on classroom approach can help pregnant women learn and adopt healthier habits compared to traditional lectures.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 136 (estimated) |
| Ages | 20 Years to 45 Years |
| Sex | Female |
| Sponsor | Peking Union Medical College Hospital Academic / other |
| Locations | 1 site (Beijing) |
| Trial ID | NCT06413303 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the impact of an experiential classroom approach on establishing healthy behaviors among pregnant women. It aims to address adverse pregnancy outcomes by focusing on preconception education and encouraging active participation through peer discussions and reflections. The study involves a multi-center, randomized controlled design to evaluate the effectiveness of this innovative educational method compared to traditional lectures. By fostering an engaging learning environment, the trial seeks to empower women to adopt healthier lifestyles during pregnancy.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women over 20 years old, in their first trimester, with singleton pregnancies who can attend regular prenatal follow-ups.
Not a fit: Patients with severe mental illness, significant liver or kidney impairment, malignant tumors, or contraindications to exercise during pregnancy may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the incidence of adverse pregnancy outcomes and improve maternal and fetal health.
How similar studies have performed: While traditional educational methods have shown limited effectiveness, this experiential approach is relatively novel and has not been extensively tested in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Older than 20. * Singleton pregnancy. * The first trimester. * Be able to undergo regular prenatal follow-ups and delivery in PUMCH. * Be able to participate in each experiential classroom on time. * Capable of independently completing questionnaire surveys. Exclusion Criteria: * With severe mental illness. * Severe impairment of liver and kidney function. * With malignant tumors. * With contraindications to exercise during pregnancy.
Where this trial is running
Beijing
- Department of ob gyn, Peking Union Medical College Hospital — Beijing, China (Recruiting)
Study contacts
- Study coordinator: Liangkun Ma
- Email: maliangkun@pumch.cn
- Phone: 13021961166
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.