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 @ 12:06 AM
Ignite Modification Date:
2025-12-25 @ 12:06 AM
NCT ID:
NCT05820958
Eligibility Criteria:
Inclusion Criteria:
* first physiological delivery;
* no previous miscarriages;
* normal course of pregnancy;
* normal fetal development confirmed by prenatal ultrasound examination;
* consent to the intervention in the form of intensifying tactile contact with the child during the observation period.
Exclusion Criteria:
* poor health of the child after birth, Apgar score\< 8 points;
* complicated physiological delivery with accompanying poor physical condition of the mother after delivery (deep vein thrombosis, pulmonary embolism, postpartum hemorrhage, inflammation);
* deterioration of the child's health condition preventing contact between mother and child (child's illness, incubation of the child);
* deterioration of the mother's health during the observation period;
* deterioration of the mother's emotional state during the observation due to external factors, such as sudden deterioration of the financial situation, traumatic family events (death, severe illnesses, accidents, etc.), significant deterioration of partnership relations between the child's parents, emotionally burdensome legal problems.
* lack of proper compliance with intervention procedures in the form of intensifying tactile contact with the child, the number of procedures performed \<50% of the recommended number.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT05820958
Study Brief:
Protocol Section:
NCT05820958