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NCT01210300 Clinical Trial

Exploring Taiwanese Womens' Decision-making Regarding Vaginal Birth After Caesarean Section

Caesarean Section Clinical Trial

Official title:
Exploring Taiwanese Womens' Decision-making Regarding Vaginal Birth After Caesarean Section

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01210300
Other study ID # 99038
Secondary ID
Status Completed
Phase N/A
First received September 26, 2010
Last updated April 22, 2011
Start date June 2010
Est. completion date September 2010

Study information
Verified date April 2011
Source Taipei Medical University WanFang Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

The incidence of caesarean section (CS) has increased globally. Taiwan's statistics report a higher incidence of repeat CS compared to vaginal birth after caesarean (VBAC). This is concerning, as repeat CS are associated with increased maternal morbidity and mortality, and neonatal respiratory problems. VBAC is an approach which reduces the likelihood of such birth complications. However, there is limited information about Taiwanese women's decision regarding VBAC and their participation in decision-making. There is also a gap in literature about information for women about CS and VBAC.

Description:

Ajzen's Theory of Planned Behaviour will theoretically underpin the study. A qualitative descriptive design using purposive sampling of 20 Taiwanese pregnant women who have previously had a CS with a live baby will be recruited from Chang Gung Memorial Hospital in Taiwan. In-depth interviews will be carried out in three phases: (1) between 34 weeks to 38 weeks of women's pregnancy; (2) on the third day after childbirth; and (3) at the fourth week after birth, the end of confinement. Boyatzis' Data Driven approach will be adopted to thematically analyze the data.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date September 2010
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Have had a previous CS with a live baby

- Currently at 34 to 38 weeks of pregnancy

- Medically eligible for a VBAC

- Have chosen to have a natural birth

- 20 years old and over

- Able to converse in Mandarin and/or Taiwanese

Exclusion Criteria:

- Previous myomectomy

- Previous classical caesarean section

- Two previous caesarean section

- Pregnant with complications

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Taiwan Chang Gung Institute of Technology Taoyuan

Sponsors (1)
Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital

Country where clinical trial is conducted

Taiwan, 

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