Skip to content

Pathophysiology during neural information processing in ADHD

Pathophysiology during neural information processing in ADHD

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00014922
Enrollment
32
Registered
2018-07-18
Start date
2017-11-20
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

F90

Interventions

Group 1: This is a non-interventional study (EEG, neuropsychological testing, interview), which is independent of the clinical drug treatment with methylphenidate. Amendment 1: unmedicated adult pati

Sponsors

Klinik für Psychiatrie und Psychotherapie der Uniklinik Köln
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Amendment 1+2: 1) Age 18-45 2) Sufficient understanding of the German language for the questionnaire survey 3) Written informed consent of patients 4) Diagnosis of ADHD according to ICD-10 5) Clinically indicated treatment with methylphenidate 6) Stable psychotropic medication (except ADHD medication) for at least 4 weeks Amendment 1: unmedicated, concerning methylphenidate Amendment 2: Medicated for at least 6 months with methylphenidate

Exclusion criteria

Exclusion criteria: 1. known neurological disorders affecting the brain, including condition after craniocerebral trauma with unconsciousness greater than 5 minutes 2. harmful substance use according to ICD-10 3. taking antipsychotics up to 4 weeks before baseline and during the examination period For Amendment 1: 4. taking pharmaceuticals for ADHD treatment on the day of the examination (not extended release) or within 48 hours (extended release and atomoxetine) before baseline For Amendment 2: 4. taking pharmaceuticals for ADHD treatment on the day of the examination (not extemded release) or within 48 hours (extended release and atomoxetine) before baseline, with the exception of methylphenidate 5. motor hyperactivity at the time of measurement that makes an EEG examination impossible 6. known IQ < 70 7. premature birth < 32 wks

Design outcomes

Primary

MeasureTime frame
Evidence of specific changes in the EEG relative to medication

Secondary

MeasureTime frame
Relationship between EEG parameters, dosage of medication, neuropsychology and interviews on the current condition (ADHS-E, Wender Utah Rating Scale short form (WURS-K), Wender-Reimherr-Interview (WRI-V), Testbatterie zur Aufmerksamkeitsprüfung (TAP))

Countries

Germany

Contacts

Public ContactRalf Müller

Klinik für Psychiatrie und Psychotherapie der Uniklinik Köln

ralf.mueller@uk-koeln.de0221 478 86238

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026