The main objective is to assess whether there are factors associated with women's refusal to participate in a randomized clinical trial involving first-trimester screening for pre-eclampsia. The secondary objective is to qualitatively evaluate the reasons for acceptance and refusal to participate.
1. Determine the acceptance/refusal rate among all women identified, eligible and offered RCT. 2. Comparison of demographic characteristics between the two groups * Group 1: women accepting to participate in RCT * Group 2: women refusing to participate in RCT 3. Assessment of motivations for acceptance (based on questionnaire given to women who agree to participate) 4. Evaluation of reasons for refusal to participate - obstacles (based on the questionnaire given to women who refuse to participate).
Study Type
OBSERVATIONAL
Enrollment
472
Questionnaire about acceptance
Questionnaire about refusal
Port-Royal Maternity
Paris, IDF, France
Factors associated with women's refusal
The primary objective is to assess whether there are factors associated with women's refusal to participate in the RANSPRE randomized clinical trial.
Time frame: Day 1
Number of acceptations
Time frame: Day 1
Number of refusals
Time frame: Day 1
Demographic characteristics
Time frame: Day 1
Questionnaire "acceptance"
Evaluation of motivations linked to acceptance (based on the questionnaire given to women who agree to participate) The secondary objective is to qualitatively assess the reasons for acceptance of participation.
Time frame: Day 1
Questionnaire "refusal"
Evaluation of the reasons for refusing to participate - obstacles (based on the questionnaire given to women who refuse to participate). The secondary objective is to qualitatively assess the reasons for refusal of participation.
Time frame: Day 1
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