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:
2025-12-24 @ 3:56 PM
Ignite Modification Date:
2025-12-24 @ 3:56 PM
NCT ID:
NCT01260792
Eligibility Criteria:
Inclusion Criteria:
* Child known for the teacher for at least three months so that his evaluation Reflect most faithfully possible the usual behavior of the child,
* Child having the Frenchman for mother tongue to avoid the consequences on him Behavior of a linguistic obstacle,
* Authorization to use the data signed by at least one of the parents of the child and by the very child when he is old at least of six years.
* Parents speaking and reading the Frenchman.
Exclusion Criteria:
* Child known to follow a specific treatment of a disorder(confusion)attentional with / without Hyperactivity-impulsiveness (eg. Ritaline Ò, Ritaline Ò LP, Arranged Ò LP, Strattera Ò) Whatever is its duration. Indeed, a selection on this criterion would introduce a way Major which(who) would return the less reliable results(profits) of the study.
* Child presenting a known neurological or psychiatric disorder, or a deficit Intellectual because the attentional disorders(confusions), the psychomotor excitement and The impulsiveness can be symptoms inherent to the other pathologies Neurological and\\or psychiatric.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
5 Years
Maximum Age:
18 Years
Study:
NCT01260792
Study Brief:
Protocol Section:
NCT01260792