Trials / Recruiting
RecruitingNCT05840367
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
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 15 (estimated)
- Sponsor
- Sygehus Lillebaelt · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Partner 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. |
Timeline
- Start date
- 2023-06-01
- Primary completion
- 2024-11-30
- Completion
- 2024-12-31
- First posted
- 2023-05-03
- Last updated
- 2024-04-26
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT05840367. Inclusion in this directory is not an endorsement.