Ignite Creation Date:
2024-05-06 @ 6:58 PM
Last Modification Date:
2024-10-26 @ 2:57 PM
Study NCT ID:
NCT05840367
Status:
RECRUITING
Last Update Posted:
2024-04-26
First Post:
2023-04-18
Brief Title:
Mothers Experience of Category 1 Cesarean Section
Sponsor:
Sygehus Lillebaelt
Organization:
Sygehus Lillebaelt
Study Overview
Official Title:
Mothers Experience of Category 1 Cesarean Section - in a Hospital Where the Partner is Present in the Operating Room A Qualitative Study
Status:
RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
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
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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None