Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:43 AM
Ignite Modification Date:
2025-12-25 @ 2:43 AM
NCT ID:
NCT02201433
Eligibility Criteria:
PART 1
Inclusion Criteria:
* Member of Association of Parents of premature children major (born before 37 weeks)
* Medical staff (doctors, nurses, pediatric nurses, social worker, ...) working in the NICU of the study.
* Signing of free and informed consent
PART 2
Inclusion Criteria:
* major fathers of child born before 37 weeks who survived to the early neonatal period (7days),
* French mother tongue,
* Residing in the geographical area of Brest
* Signing of free and informed consent
* Inclusion between Day 7 and Day 30 after the birth of their child
PART 3
Inclusion Criteria:
* fathers who have experienced child born premature
* caregivers of NICU
PART 1, 2 and 3 exclusion criteria:
* Person whose refuse to participate
* Persons unable to consent
* Persons whose monitoring is impossible
* minor
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02201433
Study Brief:
Protocol Section:
NCT02201433