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Study aim
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To determine the effectiveness of a comprehensive intervention package in reducing fear of childbirth and improving childbirth self-efficacy, maternal satisfaction, and childbirth outcomes.
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Design
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A randomized, controlled, parallel-group, double-blind clinical trial with assessor and data analyst blinding will be conducted among 60 pregnant women. Randomization will be performed using a computer-generated block randomization sequence.
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Settings and conduct
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The study will be conducted at prenatal care clinics, comprehensive health centers, and affiliated hospitals of Isfahan University of Medical Sciences, Iran. Eligible pregnant women will be recruited during routine antenatal care visits, randomly allocated to the intervention or control group, and followed from 28–30 weeks of gestation until childbirth.
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Participants/Inclusion and exclusion criteria
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Inclusion criteria
Low-risk pregnant women, 28–30 weeks of gestation, W-DEQ ≥60, and willing to participate.
Non-inclusion criteria
High-risk pregnancy, indication for cesarean birth, severe psychiatric disorders, or withdrawal from the study.
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Intervention groups
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Participants will receive antenatal care based on a comprehensive intervention package including education, counseling, relaxation techniques, and use of a mobile application from 28–30 weeks of gestation until childbirth.
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Main outcome variables
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Fear of childbirth (W-DEQ), childbirth self-efficacy (CBSEI), and maternal satisfaction with vaginal birth.