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Refusal to Participate in a Randomized Trial Involving Pregnancy and Childbirth: Factors Associated With Refusal and Reasons for Refusal and Acceptance

NCT06612320 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 526

Last updated 2026-04-08

No results posted yet for this study

Summary

The main objective is to assess whether there are factors associated with women's refusal to participate in a randomized clinical trial involving pregnancy and childbirth in France. The secondary objective is to qualitatively evaluate the reasons for acceptance and refusal to participate.

Conditions

  • Pregnancy Related

Interventions

BEHAVIORAL

Questionnaire about acceptance

Questionnaire about acceptance

BEHAVIORAL

Questionnaire about refusal

Questionnaire about refusal

Sponsors & Collaborators

  • URC-CIC Paris Descartes Necker Cochin

    collaborator OTHER

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Yoann Athiel, MD · Port-Royal Maternity - APHP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-31
Primary Completion
2025-10-28
Completion
2025-10-28

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06612320 on ClinicalTrials.gov