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Clinical Trials/NCT02609217
NCT02609217
Unknown
Not Applicable

Parents' Expectations and Experiences Around Cesarean Section in Belgium

Universitaire Ziekenhuizen KU Leuven1 site in 1 country24 target enrollmentNovember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cesarean Section
Sponsor
Universitaire Ziekenhuizen KU Leuven
Enrollment
24
Locations
1
Primary Endpoint
Information on parents' fears and expectations around cesarean section
Last Updated
10 years ago

Overview

Brief Summary

The aim of this study is to gain insight in the experiences and expectations of Belgian parents concerning primary cesarean section. This will be achieved by structured patient interviews and questionnaires in 24 women undergoing the procedure and their partners. This group will be divided into two subgroups of 12 multiparous and 12 nulliparous women and their partners.

Detailed Description

The subjects in both groups will be interviewed twice and will receive three questionnaires. One to two weeks prior to the scheduled cesarean section and during a scheduled obstetric outpatient visit, the first interview and questionnaire will be administered to the couple. A second questionnaire will be provided while still hospitalized (5 days post partum), to both mother and partner. Six weeks post partum, during a scheduled obstetric outpatient visit, the couple will be interviewed for the last time and will be asked to complete the third and last questionnaire.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
May 2016
Last Updated
10 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

prof. dr. Tim Van Mieghem

Assistant professor

Universitaire Ziekenhuizen KU Leuven

Eligibility Criteria

Inclusion Criteria

  • Pregnant women
  • Partner available
  • 18-50 years of age
  • Singleton pregnancy
  • Booked for planned cesarean section ≥37 weeks of gestation
  • Dutch-speaking
  • Informed consent given

Exclusion Criteria

  • Emergency cesarean section
  • \<18 years of age or \>50 years of age
  • Multiple pregnancy
  • Inability to provide consent (language, etc.)
  • Partner not consenting
  • BMI \>35 kg/m2
  • Maternal or fetal pathologies expected to affect pre and postnatal maternal/neonatal management

Outcomes

Primary Outcomes

Information on parents' fears and expectations around cesarean section

Time Frame: 6 weeks post partum

Information on parents' fears and expectations around cesarean section will be obtained using structured patient interviews and questionnaires.

Secondary Outcomes

  • Quantitative data on postoperative pain after cesarean section(6 weeks post partum)
  • Data on frequency of breastfeeding after cesarean section(6 weeks postpartum)
  • Data on the experience of postoperative pain after cesarean section(6 weeks postpartum)
  • Data on the experience of breastfeeding after cesarean section(6 weeks postpartum)
  • Qualitative data of breastfeeding after cesarean section(6 weeks postpartum)

Study Sites (1)

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