Study of Psychomotor Development and Attachment in Children Aged 6 to 30 Months With Oral Disorder (NCT03671551) | Clinical Trial Compass
TerminatedNot Applicable
Study of Psychomotor Development and Attachment in Children Aged 6 to 30 Months With Oral Disorder
Stopped: Recruitment too low
France1 participantsStarted 2018-11-19
Plain-language summary
Dietary difficulties and eating disorders of the child are a common reason for consulting infants and young children. There is currently little data on the psychomotor development of these children and their association with parent-child attachment. The objective of this study is to evaluate, at the same time, the three physiological, psychomotor and attachment dimensions of children with eating disorders.
Who can participate
Age range
6 Months – 30 Months
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:
* Age: 6 to 30 months
* Oral disorder defined by a MCH score ≥ 61
Exclusion Criteria:
* Children in enteral nutrition asked for an indication other than oral disorders
* Children followed for serious chronic organic pathology causing disorders of the oral (DNTC, swallowing disorders, etc.)
* Child already assessed by the psychomotrician who participated in the study
* Placement of the child in a medical institution or in a foster family.
* Parents' refusal to participate in the study
* Establishment of a psychomotor follow-up between the time of the medical consultation and the psychomotor evaluation.
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.