Multi Neuro-functional Biomarkers for Monitoring the Effects of Treatments in ADHD Children
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- STATUS
- Recruiting
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- participants needed
- 20
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- sponsor
- IRCCS Eugenio Medea
Summary
MIMOSA study aims to characterize from behavioral, neurophysiological and neurocognitive perspectives children and adolescents with attention deficit hyperactivity disorder (ADHD), in order to identify a possible biomarker of response to medication treatments. To achieve this aim, in the study children with ADHD (drug naive) are recruited and undergo behavioral and clinical screenings, neurocognitive profile, and neurophysiological evaluation with functional near infrared spectroscopy (fNIRS). ADHD group is evaluated before the beginning of medications, at first dose of medication (only imaging evaluation fNIRS), and after a period of two/three months of continuous treatment with medication.
Details
| Condition | Oppositional Defiant Disorder, Attention deficit hyperactivity disorder |
|---|---|
| Age | 6years - 18years |
| Treatment | Methylphenidate |
| Clinical Study Identifier | NCT04272021 |
| Sponsor | IRCCS Eugenio Medea |
| Last Modified on | 19 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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