- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03141320
Confident Birthing: What Influences Women's Confidence for Birth?
Confident Birthing: A Qualitative Study Exploring the Influences on Women's Confidence for Birth During Pregnancy and Labour
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study aims to help women have a better birth experience, by trying to understand what a 'confident birth' means to women during pregnancy and labour. Results from a recent service evaluation at a local NHS Trust, exploring a new programme designed to enhance women's birth experience, highlighted the importance of understanding women's confidence for birth. A significant number of pregnant women that attended the course (19.5%) felt 'not at all confident' for birth. The service evaluation results also suggested that confidence for birth is an important influence of enhancing birth experience.
There is some research that suggests that if women's confidence for birth can be improved, then she may be less fearful of birth and have experience less labour pain. However, very little is known about what women consider to be a 'confident birth' and who or what they feel influences their confidence. If maternity services are able to understand this, this could possibly lead to the development of tools and strategies to help women to feel more confident for giving birth.
This is a qualitative study that involves two methods of data collection: interviews and social media. Women that are pregnant or have recently given birth will be interviewed to explore who or what they feel has influenced their confidence for birth. The interviews will last for about one and a half hours. The location for interview is flexible and women can be interviewed in their own home. In addition to this, approximately 500 messages posted on a large UK parenting website about confidence for birth will also be analysed.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- given birth within the last two years or are pregnant
- consider themselves well enough to take part in the study
- have received maternity care from specific NHS Trust
Exclusion Criteria:
- under 18 years old
- have not received maternity care from specific NHS Trust
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Semi-structured interviews
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 20007
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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