- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07616765
Women's Knowledge About Induction of Labour and Its Association With Their Experience (INFORM)
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.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
La description
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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Women's Pre- Induction knowledge of induction of labour
Délai: 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.
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Adhésion et conformité au traitement
- Comportement de santé
- Comportement
- Satisfaction des patients
- Qualité des soins de santé, accès et évaluation
- Techniques d'investigation
- Méthodes épidémiologiques
- Collecte de données
- Mécanismes d'évaluation des soins de santé
- Qualité des soins de santé
- Santé publique
- Environnement et santé publique
- Enquêtes et questionnaires
Autres numéros d'identification d'étude
- 179390
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