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

IMPACT OF BREATH CONTROL AND RETENTION ON PATIENT STRESS. E.S IN MEDICALLY ASSISTED REPRODUCTION BREATH HOLD TO BREATH BETTER PROGRAM IN MEDICALLY ASSISTED REPRODUCTION

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06357208
Acronym
BHBB
Enrollment
12
Registered
2024-04-10
Start date
2024-05-06
Completion date
2024-07-01
Last updated
2024-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reproductive Disorder

Brief summary

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

Detailed 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.

Interventions

OTHERBreathing Control and Retention

4 appointments with training of Breathing Control and Retention

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Rate of stressed patientsmonth 1with score of 27 on the Perceived Stress Scale

Secondary

MeasureTime frameDescription
STAI Y-A (anxiety state) scalemonth 1feeling anxious at the time with a score \> 39 for men and \> 47 for women

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026