Skip to main content
OpenTrials
Completed

NCT Number: NCT03084354

Women's Experiences of Maternity Bladder Care

Background.

Although a healthy urinary system is a vital aspect in every woman's life, bladder management is an aspect of maternity care, which is, or perceived as, being poorly managed by health care professionals. Furthermore, although the relationship between childbirth and bladder dysfunction is an incontestable fact very well documented in the medical literature, women's experiences of bladder care have not been recognized by the evidence, and therefore, no research has been developed to address this topic. This fact implies a limited level of awareness and degree of implication from women in this matter.

Research question.

What are women's experiences, perceptions and knowledge of bladder care during the antepartum, intrapartum and postpartum period?

Aim.

To explore women's experiences of bladder care during the antepartum, intrapartum and postpartum period.

Design.

Exploratory, descriptive research study.

Population.

Women who have given birth to a singleton, live, term baby between two weeks and six months prior the study, and who meet the inclusion and exclusion criteria.

Methods.

In-depth semi-structured interviews.

Sample.

A purposive sample of eight to sixteen women, with a heterogeneous representation of the different modes of birth, will be sought.

Recruitment.

Postnatal midwives will act as gatekeepers identifying potential participants and providing information packs. Other recruitment resources will include posters and a study website, which will be advertised at local maternity groups.

Data collection.

Semi-structure interviews to gain a deep understanding of women's experiences of maternity bladder care. Interviews will last between thirty minutes to a couple of hours and they will be digitally recorded and transcribed verbatim.

Data Analysis.

Framework analysis assisted by memoing technique.

Ethical considerations.

Ethical approval from the Sponsor and the Health Research Authority will be sought.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

University of Southampton

Southampton, Hampshire, SO17 1BJ, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women who have received antepartum, intrapartum and postpartum care at the designated hospital.
  • Women who have given birth to a live singleton, term (37 to 42 weeks gestation) infant between two weeks and six months ago at the designated hospital.
  • Women who have been identified and received the information pack by the named postnatal midwife. Alternatively, potential participants can also get included in the study after being self-referred through local maternity groups (posters, leaflets, (PDF file) webpages and study website).

Exclusion criteria

  • Women and newborns with serious medical/life threatening conditions (pre-existing mental health, neurological, uro-genital conditions, pregnancy related complications and/or newborn related conditions, such us, preterm delivery, fetal abnormalities, admission to the neonatal unit and poor condition at birth).
  • Women who have experienced a stillbirth, neonatal death or traumatic birth.
  • Women who are not fluent in English, although Spanish participants will be included as the main researcher is fluent in both languages.
  • Women under the age of eighteen.
  • Women who are unable to be interviewed due to cognitive impairment or disabilities.

Treatment and study plan

semi-structured interviews

Other

Semi-structure interviews to gain a deep understanding of women's experiences of maternity bladder care. Interviews will last between thirty minutes to a couple of hours and they will be digitally recorded and transcribed verbatim.

Primary outcomes

  1. Women's experiences of bladder care during the antepartum, intrapartum and postpartum period

    Time frame: day 1

    Qualitative semi-structured interviews performed at one occasion where the participant describes her experience of bladder care during pregnancy, labour and after birth.

Sponsors and collaborators

Lead sponsor

University of Southampton

Other

Collaborators

  • National Institute for Health Research, United Kingdom

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Mar 20, 2017
Registry last updated
Jul 13, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.