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Symptom and behavior characterization in everyday life with ADHD in adulthood: a mobile virtual reality assessment

Symptom and behavior characterization in everyday life with ADHD in adulthood: a mobile virtual reality assessment - VSR-CB

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00034271
Enrollment
42
Registered
2024-12-19
Start date
2025-04-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F90

Interventions

Group 1: Adults with ADHD according to DSM-V or ICD-10 (experimental group) perform a neurpsychological task to measure sustained attention, which is integrated into a virtual reality (VR), first once

Sponsors

Klinik und Poliklinik für Psychiatrie und Psychotherapie Universitätsklinikum Bonn
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: - Sufficient understanding of the German language - Normal or corrected vision - Access to an Android or Apple smartphone - Current diagnosis of ADHD according to DSM-V or ICD-10 (experimental group)

Exclusion criteria

Exclusion criteria: - Psychotic symptoms, bipolar disorder, manic symptoms - Diseases from the schizophrenia spectrum - Substance dependence - Taking psychotropic drugs for the treatment of ADHD or antidepressants - Epilepsy or other neurological diseases - Pregnancy - Current diagnosis of ADHD or affective disorder according to DSM-V or ICD-10 (control group)

Design outcomes

Primary

MeasureTime frame
The primary objective is to compare the performance in the neuropsychological task, i.e. reaction time, reaction time variability, omission and commission errors at the baseline in the laboratory and four further time points at home between the two groups.

Secondary

MeasureTime frame
As secondary target variables, the head movements at the individual measurements will be compared between the two groups and a subjective symptom query will be included in the analysis after each measurement. Furthermore, the user-friendliness of the mobile setup used is to be investigated and the comparability of the stationary and mobile setups is to be examined.

Countries

Germany

Contacts

Public ContactNiclas Braun

Klinik und Poliklinik für Psychiatrie und Psychotherapie Universitätsklinikum Bonn

niclas.braun@ukbonn.de0228-28715723

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026