Women's Knowledge About Induction of Labour and Its Association With Their Experience

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorImperial College London

About this trial

Induction of labour (IOL) is a common procedure to initiate childbirth, around one in three pregnant women having their labour induced in the UK. Labour may be induced for many different reasons, including going past the due date, having high blood pressure, diabetes, concerns about the baby's growth, or reduced movements.

IOL can be a complex and lengthy process, sometimes lasting up to seven days. Many women find that their expectations of IOL do not match their real experiences. Research shows that between 5% and 20% of women report a negative birth experience, and this can have lasting effects. These may include difficulties bonding with their baby, depression after birth, fear of future childbirth, or choosing a caesarean section next time.

Studies also show that women who feel unprepared for induction, or who do not fully understand the benefits, risks, and steps involved, are more likely to have a difficult experience. At the same time, research suggests that some healthcare professionals may not feel fully confident in their knowledge of induction, and their decisions may be influenced by colleagues or local practice rather than evidence alone.

This project aims to understand how much women know about induction before it begins, how this knowledge affects their experience, and how well clinicians understand and communicate about induction.

To do this, investigators will invite women who are booked for induction at Chelsea and Westminster Hospital or West Middlesex Hospital to take part in two surveys: one before induction and one after birth. Women will also be able to volunteer for an interview to talk in more detail about their experience. They will also invite all maternity staff at the Trust to complete a short survey about their knowledge and attitudes towards induction, followed by optional interviews.

Investigators aim to recruit approximately 82 pregnant women and 20 to 30 clinicians (including midwives, obstetricians, and trainees) working in the maternity department at Chelsea and Westminster Hospital NHS Foundation Trust.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All pregnant women who are booked for IOL at Chelsea and Westminster Hospital NHS Foundation Trust which includes both Chelsea and Westminster Hospital and West Middlesex Hospital.

The ability to understand and sign a written informed consent form.

Singleton pregnancy.

Disqualifiers

Under age 18

Women who do not have sufficient understanding of the English language to provide informed consent or to complete the questionnaires and interviews independently

Those not meeting the inclusion criteria

Trial population

Pregnant women aged 18 and over who are booked for induction of labour at Chelsea and Westminster Hospital NHS Foundation Trust (including Chelsea and Westminster Hospital and West Middlesex Hospital), and clinicians (midwives, obstetricians, and trainees) working in the maternity department at the same Trust.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Survey and Interview-Based Assessment

    Other intervention

    Participants will complete questionnaires and/or take part in semi-structured interviews to assess their knowledge and experiences related to induction of labour.

Treatment groups

112 Participants
are divided into 2 treatment groups
Group A: Pregnant women booked for induction of labour - 82 participants1 intervention
Group B: Clinicians in maternity at Chelsea and Westminster Hospital NHS FT, 20-30 participants1 intervention

Trial outcomes

Primary outcomes

1

Women's Pre- Induction knowledge of induction of labour

Assessment will be performed using the Pre-Induction Survey, with a maximum score of 55.

Time frame
The project will take 24 months.

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: