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The Effect of Experiential Classroom on Establishing Healthy Behaviors During Pregnancy

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Enrolling

Conditions

Preconception Education
Experiential Classroom
Adverse Pregnancy Outcome
Health Behavior

Treatments

Behavioral: Experiential Classroom

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

A multi-center, prospective, randomized controlled clinical trial was conducted to explore the effect of experiential classroom on establishing healthy behaviors during pregnancy.

Full description

Adverse pregnancy outcomes, including maternal complications (eg, gestational hypertension, preeclampsia (PE), gestational diabetes mellitus (GDM), placental abruption) and fetal complications (eg, preterm birth, intrauterine growth restriction, large for gestational age (LGA), small for gestational age (SGA), macrosomia) , pose a significant public healthy problem which needs to be addressed. Several studies found that the health status and behaviors of mothers during pregnancy, including dietary patterns, physical activity and emotional well-being, not only affect pregnancy outcomes such as GDM and PE, but also have the long-term implications for the health of the offspring. Therefore, through effective preconception education, helping pregnant women establish healthy behaviors during pregnancy is of great significance in reducing the incidence of adverse pregnancy outcomes. However, traditional educational methods, mostly in the form of face-to-face lectures, have proven to be ineffective. On the other hand, experiential classroom emphasizes putting pregnant women at the center, based on their subjective willingness and previous knowledge and experience, creating an environment for free discussion, exchange, and reflection, and utilizing peer education to fully mobilize the subjective initiative of pregnant women. This approach allows them to explore, discuss, reflect, and learn autonomously, aiming to truly absorb, master, and apply theoretical knowledge. Therefore, to explore the impact of experiential classroom on the establishment of healthy behaviors during pregnancy, we conducted a multicenter, prospective, randomized controlled clinical trial. The study included pregnant women aged 20 and above, married, with singleton pregnancies in early pregnancy, who were randomly assigned to either the experiential classroom group or the routine prenatal care group. Both groups received routine prenatal care. The pregnant women in the personalized exercise guidance group learned about perinatal health knowledge under the guidance of multidisciplinary teachers and were supervised and managed through WeChat groups. The primary outcome measure was the total weight gain during pregnancy.

Enrollment

136 estimated patients

Sex

Female

Ages

20 to 45 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

136 participants in 2 patient groups

Experiential Classroom Group
Experimental group
Description:
Participants accept experiential class to establish healthy behaviors. They are also managed continuously through WeChat group chat during prenatal clinical interval.
Treatment:
Behavioral: Experiential Classroom
Standard Clinic Prenatal Care Group
No Intervention group
Description:
Participants accept regular routine prenatal care following Chinese standard.

Trial contacts and locations

1

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Central trial contact

Liangkun Ma

Data sourced from clinicaltrials.gov

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