MOther-Child Interaction Assessment TRAINING for Pediatricians (NCT03300713) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
MOther-Child Interaction Assessment TRAINING for Pediatricians
France3,504 participantsStarted 2017-12-02
Plain-language summary
The originality of the MOCITRAINING study lies in the integration of infant and maternal care during the pediatric consultation and the assessment of the impact of this type of care in the short and medium term on The MOCITRAINING program could contribute to improving the quality of parent-child interactions.
Who can participate
Age range
23 Days – 37 Days
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Each child will be included WITH his biological mother at the first-month visit after birth.
* Age: 1 month + / - 15 days (child), accompanied by his biological mother
* Mother able to read French;
* Signed consent letter after complete information of parents about the MOCITRAINING study, its principle, advantages and disadvantages.
Exclusion Criteria:
* Preterm babies.
* Children from a twin or multiple pregnancy.
* Children with somatic diagnosis explaining the presence of digestive, sleeping or interactional disorders.
* Refusal to participate after clear information about the study;
* Refusal to sign the consent letter;
* Refusal to be informed of a diagnostic hypothesis;
* Participants not covered by the Social Security system;
* Participants incapable of consenting or under legal protection (guardianship or curatorship).
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Frequency of pathological Alarm Distress BaBy (ADBB) scores