Comparison Between a Mindfulness-Based Program and Standard Therapeutic Follow-Up During Pregnancy
Recruiting
N/A
Interventional Study
Mindfulness Protocols
Pregnancy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 70 (estimated)
- Sponsor
- Universite Cote d'Azur · Other
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About This Trial
This study aims to evaluate the effects of a 6-week mindfulness meditation program in pregnant women, compared with a psychological support control program.
Participants in the mindfulness arm will complete one instructor-led meditation session per week and five guided audio meditation sessions at home each week.
The primary objectives are to determine whether the mindfulness program leads to:
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Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant women between 3 and 7.5 months of gestation (12-28 weeks).
* Ability to speak and read French sufficient to understand study documents and complete questionnaires.
* Willingness to participate in the study and to be randomized to one of the study groups.
Exclusion Cr…
Contacts
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