NCT07329673Suspended
An Examination of the Performance of QbMobile in Differential Diagnosis Associated With ADHD Symptoms
An Examination of the Performance of QbMobile in Differential Diagnosis Associated With ADHD Symptoms.
Source: ClinicalTrials.gov · Last updated 25 Sept 2026
Brief summary (registry, in English)
The purpose of this study is to evaluate QbMobile's ability to collect objective data to identify specific symptom profiles in differential diagnoses (ASD, MDD, Bipolar Disorder and Anxiety Disorder) that are common with ADHD.
- Status (registry)
- Suspended
- Study type
- Observational
- Enrollment
- 300 (estimated)
- First submitted
- 11 Dec 2025
- Start date
- 1 Jan 2026
- Primary completion date
- Nov 2027
- Lead sponsor
- Qbtech AB
- Diseases
- Autism, Depression
- NCT number
- NCT07329673
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Has a concurrent medical diagnosis that could significantly affect test performance such as brain injuries, Parkinson's disease, current epilepsy or active seizures, amyotrophic lateral sclerosis (ALS), multiple sclerosis, dementias (e.g. vascular dementia, Alzheimer disease, etc);
- Use of prescription medications (e.g., anxiolytics, sedative medications) taken on the day before completing QbMobile that could significantly affect performance;
- Substance use (e.g., alcohol, drugs) that may affect performance on the day of the tests.
Other illness
- Has a DSM-5 or ICD-11 diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder, brief psychotic disorder, psychotic disorder due to another medical condition, PTSD, antisocial personality disorder, or borderline personality disorder;
- Has other conditions that could affect test performance (migraine or other types of severe headache, chronic or acute pain);
Other
- Intellectual disability designated by IQ<70;
- Has a primary diagnosis of ADHD (combined, inattentive, or hyperactivity/impulsive presentation);
Who the study is looking for
- 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 initial assessment for ASD, MDD, Bipolar Disorder or Anxiety Disorder (Separation Anxiety Disorder, Social Anxiety Disorder, Generalized Anxiety Disorder (GAD)) or has a prior diagnosis of one of the included disorders but is not currently receiving treatment;
- Meets DSM-5 or ICD-11 criteria for a primary diagnosis of ASD, MDD, Bipolar Disorder or Anxiety Disorder per sites standard clinical procedures;
- Have adequate sensory and physical ability to complete QbMobile;
- Possess or have access to an iPhone model that supports QbMobile.
Age in the registry: 6 years to 60 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CCM Clinical Research Group | Miami | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.