Clinical trial Recruiting at 1 site Observational Ages 18 and up

Understanding how women feel about induction and how it shapes their experience

Official title: Induction of Labour: Women's Knowledge and Experience

Run by Imperial College London · NCT07616765 · Data updated 2026-11-12

This study tests how prepared women feel about induction of labor and how that relates to their childbirth experience among those scheduled for induction at two London hospitals.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment112 (estimated)
SponsorImperial College London
Academic / other
Locations1 site (London, London)
StatusRecruiting
StartedJuly 1, 2026
Main results expectedDecember 1, 2027
Study endsMay 1, 2028
Registry record updatedNovember 10, 2026
Trial IDNCT07616765 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are pregnant women booked for induction of labor at Chelsea and Westminster Hospital NHS Foundation Trust who can understand English and provide informed consent (singleton pregnancies).

Probably not a fit

Women who do not participate may miss insights into preparedness and experiences that could inform care improvements.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study uses surveys and interviews to explore women's knowledge, expectations, and satisfaction related to induction of labor. It focuses on those booked for induction at Chelsea and Westminster Hospital NHS Foundation Trust and aims to identify factors linked to negative or positive birth experiences. The approach analyzes both patient and clinician perspectives to understand communication gaps and experiences throughout the induction process. Findings could highlight areas where education and planning might improve satisfaction and outcomes for women undergoing induction. The study is led by Imperial College London with participation limited to eligible pregnant women and clinicians at the participating sites.

Why it matters

Potential benefit: If successful, the study could guide improvements in patient education and support during induction, potentially improving satisfaction and emotional outcomes for mothers.

How similar studies have gone: Previous research suggests that better preparation and understanding of induction can improve patient experience, though this exact patient-population focus is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Women:

* 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.

Clinicians:

• Working at Chelsea and Westminster Hospital NHS Foundation Trust which includes both Chelsea and Westminster Hospital and West Middlesex Hospital.

Exclusion Criteria:

Women:

* 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

Clinicians:

• Those not meeting the inclusion criteria

Where it's running

  • Chelsea and Westminster Hospital NHS Foundation Trust
    London, London, United Kingdom
    Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.