Actively Recruiting

Age: 6Years - 60Years
All Genders
NCT07329673

An Examination of the Performance of QbMobile in Differential Diagnosis Associated With ADHD Symptoms

Led by Qbtech AB · Updated on 2026-05-06

300

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

An Examination of the Performance of QbMobile in Differential Diagnosis Associated With ADHD Symptoms

Who Can Participate

Age: 6Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Provide written informed consent (including parental or guardian consent and assent if under 18) for QbMobile
  • Aged over 6 years and under 60 years old
  • Referred for initial assessment or previously diagnosed with ASD, MDD, Bipolar Disorder, or Anxiety Disorder but not currently receiving treatment
  • Meets DSM-5 or ICD-11 criteria for primary diagnosis of ASD, MDD, Bipolar Disorder, or Anxiety Disorder according to clinical procedures
  • Have adequate sensory and physical ability to complete QbMobile
  • Possess or have access to an iPhone that supports QbMobile
Not Eligible

You will not qualify if you...

  • Intellectual disability with IQ less than 70
  • 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
  • Primary diagnosis of ADHD (any presentation)
  • Medical conditions affecting test performance such as brain injuries, Parkinson's disease, epilepsy or active seizures, ALS, multiple sclerosis, dementias
  • Conditions affecting test performance like severe migraine or chronic/acute pain
  • Use of prescription medications (e.g., anxiolytics, sedatives) the day before testing that could affect performance
  • Substance use (alcohol, drugs) that may affect performance on testing days

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CCM Clinical Research Group

Miami, Florida, United States, 33133

Actively Recruiting

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Research Team

R

Robert Nolen

CONTACT

R

Ragini Sanyal

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

6

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