IMPACT OF BREATH CONTROL AND RETENTION ON PATIENT STRESS. E.S IN MEDICALLY ASSISTED REPRODUCTION (BHBB)

Centre Hospitalier Universitaire de Nice

Status: Completed

Conditions: Reproductive Disorder

Treatments: Other: Breathing Control and Retention

Study type: Interventional

Funder types: Other

Identifiers

NCT06357208

23-AOI-06

2023-A02687-38 (Other Identifier)

Details and patient eligibility

About

the investigator 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

Full 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. The participants 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.

Enrollment: 12 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Unmarried woman and couple of women with societal infertility,
• couple with medical infertility defined as absence of pregnancy after 12 months without contraception,
• age greater than 18 years,
• patient who has signed informed consent and affiliated to social security.
• Patient available at the proposed slots over 4 weeks

Exclusion criteria

• pregnant women before starting the program,
• heart failure
• Thrombocytopenia
• epilepsy

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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12 participants in 2 patient groups

Breathing Control and Retention

Experimental group

Description:

Breathing Control and Retention

Treatment:

Other: Breathing Control and Retention

Usual follow-up

No Intervention group

Description:

the patient come at the begin of the study and come back after one month