Skip to content

Mothers' Experience of Category 1 Cesarean Section

Mothers' Experience of Category 1 Cesarean Section - in a Hospital Where the Partner is Present in the Operating Room. A Qualitative Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05840367
Enrollment
22
Registered
2023-05-03
Start date
2023-06-01
Completion date
2025-03-01
Last updated
2026-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Section Complications

Brief summary

The aim of this qualitative prospective study is to investigate how mothers experience a category 1 cesarean section in a hospital where the partner is present in the operation room during the entire process (induction of general anestesia, cesarean section, possible resuscitation of newborn). Mothers will be included in the study, if they wish to participate, on day 1 or 2 following the cesarean section and a brief, structured interview will be held concerning her experience of the cesarean section. Clinical baseline data regarding the mother, the cesarean section and the infant will be collected from patients files. Mothers will be contacted again three months after the cesarean section, and a semi-structured interview will be held via telephone. At the end of the interview a screening for posttraumatic stress will be performed, using the PTSD-8 tool. The interviews will be recorded and transscribed verbatim. Content of interviews will be analysed using manifest content analysis. NVivo software will be used for coding interviews.

Interventions

BEHAVIORALPartner present in the operation room

The partner (father, co-mother or other close relative present for the birth) is present in the operation room during the entire category 1 cesarean section. This is standard clinical practice in this particular hospital since June 2021.

Sponsors

Sygehus Lillebaelt
Lead SponsorOTHER
University of Southern Denmark
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Mothers who had a category 1 cesarean section in Kolding Hospital, Denmark during a 1-year period

Exclusion criteria

* Not speaking/understanding Danish

Design outcomes

Primary

MeasureTime frameDescription
Mothers' experience of the category 1 cesarean sectionThree months after the cesarean sectionQualitative analysis of data regarding mothers' experience of a category 1 cesarean section in a hospital where the partner is present in the operation room. Semi-structured interviews will be held, recorded digitally and transscribed. Content will be analysed qualitatively using manifest content analysis, and major themes as well as sub-themes will be identified, describing mothers' experience with the category 1 cesarean section.

Secondary

MeasureTime frameDescription
PTSDThree months after the cesarean sectionOccurence of posttraumatic stress as evaluated using the PTSD-8 tool (in Danish)

Countries

Denmark

Contacts

STUDY_CHAIRAnne C Brøchner, MD, Associate Professor

Lillebaelt Hospital Kolding, Department of Anesthesiology and Intensive Care, and University of Southern Denmark, Department of Regional Health Research

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026