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

27 maj 2026 uppdaterad av: Imperial College London

Induction of Labour: Women's Knowledge and Experience

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.

Studieöversikt

Status

Har inte rekryterat ännu

Studietyp

Observationell

Inskrivning (Beräknad)

112

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

N/A

Testmetod

Icke-sannolikhetsprov

Studera befolkning

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.

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Pregnant women booked for induction of labour - 82 participants
Participants will complete questionnaires and/or take part in semi-structured interviews to assess their knowledge and experiences related to induction of labour.
Clinicians in maternity at Chelsea and Westminster Hospital NHS FT, 20-30 participants
Participants will complete questionnaires and/or take part in semi-structured interviews to assess their knowledge and experiences related to induction of labour.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Women's Pre- Induction knowledge of induction of labour
Tidsram: The project will take 24 months.
Assessment will be performed using the Pre-Induction Survey, with a maximum score of 55.
The project will take 24 months.

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 maj 2026

Primärt slutförande (Beräknad)

1 december 2027

Avslutad studie (Beräknad)

1 maj 2028

Studieregistreringsdatum

Först inskickad

13 april 2026

Först inskickad som uppfyllde QC-kriterierna

27 maj 2026

Första postat (Faktisk)

1 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

1 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

27 maj 2026

Senast verifierad

1 maj 2026

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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