NCT07345468

Brief Summary

Objective: The aim of this research study is to evaluate the fear of childbirth, birth beliefs, and mode of birth preferences in pregnant who participated in face-to-face and online childbirth preparation classes. Method: This research is a quasi-experimental study. Pregnant will assign to two intervention groups, face-to-face, and online childbirth preparation classes. Data will collected twice, before (pre-test) and one-month after (post-test) the childbirth preparation training. The training will give face-to-face in the face-to-face classes group. The training will give online in the online classes group.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 15, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 15, 2023

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

September 24, 2025

Completed
4 months until next milestone

First Posted

Study publicly available on registry

January 15, 2026

Completed
Last Updated

January 15, 2026

Status Verified

January 1, 2026

Enrollment Period

3 months

First QC Date

September 24, 2025

Last Update Submit

January 8, 2026

Conditions

Keywords

ChildbirthFearEducationNursingParturitionPregnancy

Outcome Measures

Primary Outcomes (3)

  • fear of childbirth

    Level of childbirth fear

    before (pre-test) and one-month after (post-test) the childbirth preparation training

  • birth beliefs

    Natural or medical birth beliefs

    before (pre-test) and one-month after (post-test) the childbirth preparation training

  • mode of birth preferences

    Preferred mode of birth

    before (pre-test) and one-month after (post-test) the childbirth preparation training

Study Arms (2)

face-to-face childbirth preparation classes

OTHER

The training was given face-to-face in the face-to-face classes group

Other: face-to-face childbirth preparation education

online childbirth preparation classes

OTHER

The training was given online in the online classes group.

Other: online childbirth preparation education

Interventions

Women in the online group received online classes at the same time.

online childbirth preparation classes

Women in the face-to-face education group received face-to-face childbirth preparation classes.

face-to-face childbirth preparation classes

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Women aged 18-45 years
  • Nulliparous,
  • First and singleton pregnancy,
  • Between 20-32 weeks of gestation,
  • Without any pregnancy-related risk factors,
  • Who had not participated in any other childbirth preparation training,
  • Had at least a primary education level, had no communication difficulties,
  • Had access to and were able to use an internet-connected device with a camera.

You may not qualify if:

  • Multiparous pregnant who had multiple pregnancies,
  • Had any high-risk pregnancy symptoms,
  • Were below the 20th week and above the 32nd week.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kütahya Health Sciences University

Kütahya, 43020, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 24, 2025

First Posted

January 15, 2026

Study Start

July 15, 2023

Primary Completion

October 15, 2023

Study Completion

November 15, 2023

Last Updated

January 15, 2026

Record last verified: 2026-01

Locations