- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06062667
The Effect of Fathers' Birth Experience on Paternal Attachment and Parenting Perception: Randomized Controlled Trial
Effect Of Fathers' Bırth Experıence On Paternal Attachment And Parentıng Perceptıon: A Randomızed Controlled Study
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey, 34320
- Betül Uncu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Spouses of primiparous pregnant women who had spontaneous pregnancies and were admitted to the delivery room for normal labor were included in the study.
Exclusion Criteria:
- women without husbands
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: experimental group
Fathers will accompany their husbands during the birth process
|
Fathers will accompany their husbands during the birth process
|
|
No Intervention: Control group
routine maintenance
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The father-baby bonding of fathers who accompany their spouses in the delivery room is higher than fathers who do not accompany their spouses in the delivery room.
Time Frame: 15 days
|
Primiparous pregnant women who had spontaneous pregnancies and were admitted to the delivery room for normal labor were included in the study. In determining the groups, participants were assigned to the Fathers Who Accompany the Birth (G1) and Fathers Who Did Not Accompany the Birth (G2) groups using web-based randomization (Randomizer.org). Pregnant women and their spouses in both groups who volunteered to participate in the study had the "Information Form" filled in after admission to the delivery room, and fathers filled out PAAQ and SPPRS. Two weeks after birth, the mother and father were contacted. PPAQ and SPPRS data were obtained from fathers and EPDS data were obtained from mothers. Information Form (IF), Paternal Antenatal Attachment Questionnaire (PAAQ), Self-Perception of Parental Role Scale (SPPRS), Postnatal Paternal-İnfant Attachment Questionnaire (PPAQ) Edinburg Postnatal Depression Scale (EPDS) |
15 days
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2022/285
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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