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Comparison of the effect of Internet-based and in-person cognitive behavioral therapy on the fear of childbirth and choosing the mode of delivery in primiparous pregnant women

Comparison of the effect of Internet-based and in-person cognitive behavioral therapy on the fear of childbirth and choosing the mode of delivery in primiparous pregnant women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241111063668N1
Enrollment
72
Registered
2024-11-24
Start date
2024-12-20
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Fear of childbirth. ??? ?? ??????

Interventions

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Informed consent to participate in the study Being first pregnancy Having the age of 18 to 45 years Having a smartphone Having a fear of childbirth score higher than 85 (cut point) in the Vijima A questionnaire Reading and writing literacy at the elementary level and above Having a gestational age of 20 to 24 weeks based on the first day of the last menstrual period or an ultrasound scan under 12 weeks No smoking, alcohol or drugs The ability to communicate through a mobile phone, tablet or computer and participate in internet counseling sessions (for the internet-based cognitive behavioral therapy group) by the person himself or someone close to him who lives in the same house. Single pregnancy Absence of fetal abnormality in ultrasound Infertility through artificial insemination Not having any systemic diseases of the mother (diabetes, cardiovascular diseases, blood pressure, etc.) Not currently suffering from mental illnesses and taking neuropsychiatric drugs or a previous history thereof15. Absence of depression according to Beck Depression Questionnaire Absence of depression according to Beck Depression Questionnaire

Exclusion criteria

Exclusion criteria: Simultaneous participation in other clinical trials Emergence of scientific indication for cesarean section High-risk pregnancy for scientific reasons Intrauterine death of the fetus during the study

Design outcomes

Primary

MeasureTime frame
Fear of childbirth. Timepoint: Before the start of the intervention, immediately after the end of the intervention sessions, 4 weeks after the end of the intervention. Method of measurement: Vijima A childbirth fear questionnaire.

Secondary

MeasureTime frame
None. Timepoint: none. Method of measurement: none.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactkosar Piri

Ahvaz University of Medical Sciences

kosar.piri.199700@gmail.com+98 84 3362 6236

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026