Confident Birthing: What Influences Women's Confidence for Birth?

NCT ID: NCT03141320

Last Updated: 2018-11-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

24 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-02-01

Study Completion Date

2017-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is a grounded theory study aiming to understand women's perception of what influences their confidence for birth during labour and birth. Data is being collected using interviews and social media sources.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pregnancy Labour Birth Psychosocial Wellbeing Woman's Health

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Interview/observation of social media comments

Interview with pregnant or postnatal women and observation of relevant social media comments

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Hampshire Hospitals NHS Foundation Trust

OTHER

Sponsor Role collaborator

University of Southampton

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

20007

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

The Effect of Potcost Stories on Childbirth Fear,
NCT06740682 NOT_YET_RECRUITING NA