Fear of Childbirth, Birth Beliefs, Mode of Birth Preferences in Childbirth Preparation Classes
NCT ID: NCT07345468
Last Updated: 2026-01-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
58 participants
INTERVENTIONAL
2023-07-15
2023-11-15
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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face-to-face childbirth preparation classes
The training was given face-to-face in the face-to-face classes group
face-to-face childbirth preparation education
Women in the face-to-face education group received face-to-face childbirth preparation classes.
online childbirth preparation classes
The training was given online in the online classes group.
online childbirth preparation education
Women in the online group received online classes at the same time.
Interventions
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face-to-face childbirth preparation education
Women in the face-to-face education group received face-to-face childbirth preparation classes.
online childbirth preparation education
Women in the online group received online classes at the same time.
Eligibility Criteria
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Inclusion Criteria
* 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.
Exclusion Criteria
* Had any high-risk pregnancy symptoms,
* Were below the 20th week and above the 32nd week.
18 Years
45 Years
FEMALE
Yes
Sponsors
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Kutahya Health Sciences University
OTHER
Responsible Party
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Sevil Cicek Ozdemir
Principal Investigator
Locations
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Kütahya Health Sciences University
Kütahya, , Turkey (Türkiye)
Countries
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Other Identifiers
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KutahyaHSUU
Identifier Type: -
Identifier Source: org_study_id
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