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Clinical Trial Summary

we propose for patient in the course of Medically Assisted Reproduction a study with to arm: one arm active "Breathing Control and Retention" and the other arm control


Clinical Trial Description

After signing the informed consent, the patient makes an appointment for an exchange with the psychologist at the Reproduction center. During this exchange, the psychologist gives him the evaluation scales, explains to him when to complete them and re-explains the progress of the study. Patients in the active "Breathing Control and Retention" group make 4 appointments, one week apart, with the Bluenery Academy. They self-assess 2 days before starting the breathing program (M0), 2 days after the end of the program, 1 month after starting the program (M1). Patients in the "Usual follow-up" control group complete the self-assessments 2 days after the discussion with the psychologist (M0) and 1 month later (M1). At the end of the 2 assessments, the patient was included. sends his assessment book to the psychologist. An appointment will be made after the rating to communicate the results to them. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06357208
Study type Interventional
Source Centre Hospitalier Universitaire de Nice
Contact Valérie BENOIT
Phone 0492034702
Email benoit.v@chu-nice.fr
Status Not yet recruiting
Phase N/A
Start date May 1, 2024
Completion date December 1, 2025

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