Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06062667
Other study ID # 2022/285
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2023
Est. completion date October 1, 2023

Study information

Verified date October 2023
Source Istanbul University - Cerrahpasa (IUC)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In recent years, fathers have become increasingly involved in research, but research on fathers still lags behind research on mothers. During the transition to parenthood, a complex network of relationships emerges between father, mother and baby. During the process of becoming parents, mothers and fathers begin to bond with their unborn children. The prenatal period is hypothesized to be predictive of later postnatal attachment and perception of parenting. Paternal involvement at birth is associated with positive child health outcomes and parental well-being.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date October 1, 2023
Est. primary completion date October 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group N/A and older
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
accompany the birth
Fathers will accompany their husbands during the birth process

Locations

Country Name City State
Turkey Betül Uncu Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Istanbul University - Cerrahpasa (IUC)

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 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-Infant Attachment Questionnaire (PPAQ) Edinburg Postnatal Depression Scale (EPDS)
15 days
See also
  Status Clinical Trial Phase
Completed NCT05115071 - Online Childbirth Preparation Education in Covid-19 Pandemic N/A
Completed NCT05386004 - Labour Pain and Birth-Specific Stereogram Cards (BSSC) N/A
Completed NCT05471219 - The Effect of Focus on Vaginal Examination Experience and Pain Level: a Randomized Controlled Trial N/A
Recruiting NCT05955053 - Childbirth Performed in Collaboration With Midwife-Pregnant N/A
Completed NCT06200688 - The Effect of Peanut Ball Application on Delivery Process N/A
Completed NCT06387680 - The Peanut Ball Use on Labor N/A
Completed NCT04883541 - Effects of Yoga and Meditation on The Birth Process N/A
Completed NCT05764512 - Endorphin Massage Application to Women Who Gave Birth Vaginally N/A
Completed NCT05262231 - Online Education and Breastfeeding Motivation N/A
Completed NCT04664114 - The Effect of Virtual Reality Glass During Labor Process on Labor Pain, Birth Perception and Anxiety N/A
Recruiting NCT06020339 - The Effect of the Continuous Midwifery Care Model on Birth Outcomes N/A