CompletedNot Applicable

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

France526 participantsStarted 2024-10-31

Plain-language 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.

Who can participate

Age range18 Years

SexFEMALE

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Inclusion Criteria: The study will be offered to all women who have been offered to participate in a randomized trial relating to their pregnancy and/or childbirth in participating services. Exclusion Criteria: None

What they're measuring

Collection of maternal demographic characteristics

Timeframe: Day 1

Collection of obstetric characteristics

Timeframe: Day 1

Collection of characteristics related to information provided

Timeframe: Day 1

Trial details

NCT IDNCT06612320

SponsorAssistance Publique - Hôpitaux de Paris

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-10-28

View on ClinicalTrials.gov More Pregnancy Related trials