An Investigational Study Examining the Efficacy of QbMobile in Treatment Monitoring in Individual… (NCT07217977) | Clinical Trial Compass
By InvitationNot Applicable
An Investigational Study Examining the Efficacy of QbMobile in Treatment Monitoring in Individuals With ADHD
United States175 participantsStarted 2025-01-15
Plain-language summary
The current study will investigate if QbMobile can be used to improve the accuracy and objective identification of reduced ADHD symptoms in tests scores once treatment has been initiated.
Who can participate
Age range6 Years – 60 Years
SexALL
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Inclusion Criteria:
* Provide written informed consent (including parent/legal guardians consent when this is required for individuals under 18 years old and assent as is required based on the age of participant) for QbMobile;
* Aged \> 6 years and \< 60 years old;
* Referred for an ADHD assessment or has a diagnosis of ADHD but not currently receiving any type of stimulant or nonstimulant medication treatment;
* Meets DSM-5 or ICD-11 criteria for a primary diagnosis of ADHD (combined, inattentive, or hyperactivity/impulsive presentation) per sites standard clinical care evaluation;
* Qbtech Rating Scale total score of \>24 at Visit 1;
* Have adequate sensory and physical ability to complete QbMobile;
* Possess or has access to an iPhone model that supports QbMobile.
Exclusion Criteria:
* Intellectual disability designated by IQ\<75);
* Has used psychostimulant medication within 7 days prior to Visit 1;
* A concurrent medical diagnosis that could significantly affect test performance (brain injuries, Parkinson's disease, current epilepsy or active seizures, amyotrophic lateral sclerosis (ALS), multiple sclerosis, dementias (e.g., vascular dementia, Alzheimer disease, etc);
* Other conditions that could affect test performance (migraine or other types of severe headache, chronic or acute pain);
* Substance use (e.g., alcohol, drugs) that may affect performance on the day of the test.
What they're measuring
1
Change in QbMobile Total Score from Baseline at Visit 3 and Visit 4