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Active, not recruitingNCT05627336Updated Jul 18, 2024

Tokophobia ; Our Clinical Experience

An observational study in Tocophobia and Pregnancy Complications, sponsored by Kanuni Sultan Suleyman Training and Research Hospital. Active, not recruiting at 1 site in Turkey. Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-07-18.

Sponsored by Kanuni Sultan Suleyman Training and Research Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2025, 1 year 9 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

Fear of childbirth, or what has historically been called tokophobia, is often described as a severe fear of birth and pathological fear of childbirth. The reasons for fear of childbirth are stated as biological reasons, psychological reasons and lack of social support. However, it is still not possible to clearly explain the reasons for the fear of childbirth in pregnant women and the risk factors affecting them. The reasons for the fear of childbirth and the affecting factors have not been fully explained.

Read the detailed description

The aim of this study is to examine the relationship between fear of childbirth and anxiety sensitivity in pregnant women, and whether the mode of delivery changes depending on this fear and these data. The aim of the authors is to reveal the frequency and causes of tokophobia in pregnant women followed in their clinics and to show the birth patterns of these patients.

02

Conditions studied

  • Tocophobia
  • Pregnancy Complications

Keywords

  • vaginal birth
  • cesarean delivery
  • fear of childbirth
03

In context

Pregnancy Complications

437 studies on the registry are indexed under Pregnancy Complications; 119 are open to participants now.

This study's planned enrollment of 300 is close to the median of 320 across 205 observational studies indexed under Pregnancy Complications.

Browse Pregnancy Complications studies →

Lead sponsor

Kanuni Sultan Suleyman Training and Research Hospital is the lead sponsor of 216 studies on the registry; 34 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

3rd trimester pregnant women who are followed up in our clinic and will give birth in our clinic. Pregnant women between the ages of 18 and 40

Inclusion criteria

  • 3rd trimester pregnant women who are followed up in our clinic and will give birth in our clinic.
  • Pregnant women between the ages of 18 and 40

Exclusion criteria

Exclusion Criteria:

  • Those in the risky pregnancy category (preeclampsia, gdm, iugr... etc.)
  • Known to have fetal anomaly during follow-ups
  • Those with chronic disease
  • Those with sexually transmitted diseases
  • Those with a history of cesarean section
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Interventions

  • Diagnostic testpregnant women in the 3rd trimester

    Pregnant women who are in their third trimester and will give birth in the clinic will form the study group. These pregnant women will be measured by applying a set of questionnaires to measure their fear of childbirth.

06

What researchers measure

Primary outcomes

  1. diagnosis of tokophobia

    patients will be administered W-DEQ: Wijma Delivery Expectancy/Experience Questionnaire part A. As a result, those who score above 85 will be diagnosed with tokophobia. this test; Each question has a point equivalent, and the diagnosis will be reached by adding all the points at the end.

    Time frame: 2 months

  2. type of birth

    The birth types of patients diagnosed with tokophobia will be examined. It will be tried to show statistically whether tokophobia increases cesarean section rates or not.

    Time frame: 2 months

07

Study locations

1 site
  • Acıbadem University Atakent Hospital, Department of Obstetrics and Gynecology,
    Istanbul, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05627336
Lead sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Responsible party
Pınar Kadirogulları (Pinar KADIROGULLARI Assoc.Prof, Kanuni Sultan Suleyman Training and Research Hospital) — Principal investigator
First posted
Nov 25, 2022
Start date
Jan 1, 2023
Primary completion
Jan 1, 2025 (estimated)
Completion
Jan 1, 2025 (estimated)
Last update
Jul 18, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.

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