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Reducing Fear of Childbirth Among Pregnant Women

Reducing Fear of Childbirth Among Pregnant Women: Women's Lived Experience, Predictors, and Effects of Mindfulness-based Childbirth Education

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04214431
Enrollment
404
Registered
2020-01-02
Start date
2015-12-07
Completion date
2019-12-20
Last updated
2020-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fear of Childbirth

Keywords

fear of childbirth, pregnancy, childbirth education,

Brief summary

Pregnant women often experience fear of childbirth or anxiety toward the labor pain or uncertainties associated with labor process. To develop and evaluate the efficacy of childbirth educational interventions on reduction of fear or anxiety is an important issue in maternal health care.

Detailed description

Fear of childbirth is a common clinical problem among perinatal women and link to adverse health effects on mother's and offspring's well-being. Recently, reducing the childbirth fear becomes a highly important maternity care issues as a result of the fact that the birth rate has been declining rapidly as well as Cesarean rate increased steadily. However, the studies on fear of childbirth among perinatal population in Taiwan were limited. In this proposal the investigators plan to conduct a randomized controlled study examining the effects of mindfulness-based childbirth education. In the randomized controlled study, women will be recruited and randomized into the experiment group (receiving mindfulness-based childbirth education and traditional childbirth education),or will be allocated in the control group receiving traditional childbirth education. Intention-to-treat analysis as well as mixed regression modeling will be used to estimate the effectiveness of the interventions.

Interventions

8-week mindfulness-based childbirth education

Sponsors

Taipei Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

1. aged of 20 years or greater; 2. 12-25 week of gestation, Singleton pregnancy; 3. able to communicate with Mandarin or Taiwanese; 4. High levels of fear of Childbirth (greater 9 or above on Numeric Rating Scale).

Exclusion criteria

1. Current having psychological diseases or substance abuse, unable to follow the mindfulness-based childbirth education; 2. unable to attend every class or each assessment; 3. received any cognitive training in past one year.

Design outcomes

Primary

MeasureTime frameDescription
Fear of childbirthpregnancy 12-24 weeksFear of childbirth measure by the Wijma Delivery Expectancy/ Experience Questionnaires, W-DEQ with total score ranging between 0\ 165. The high score indicated higher levels of childbirth fear.

Secondary

MeasureTime frameDescription
Anxietypregnancy 12-24 weeksAnxiety measure by State-Trait Anxiety Inventory, STAI
Depressionpregnancy 12-24 weeksDepression measure by Edinburgh Postnatal Depression Scale, EPDS, , with a total score ranging 0,30. A higher score represents a higher level of depression.
Mindfulnesspregnancy 12-24 weeksMindfulness measure by Chinese Version Mindful Attention Awareness Scale (CMAAS), with a total score ranging 15-90, the higher score and the high levels of mindfulness.
Birth outcomespostpartum 1 weekTo analyze the mode of delivery, including vaginal delivery or cesarean delivery.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026