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The impact of Clonidine, a pharmacological treatment for attention deficit hyperactivity disorder (ADHD), on behavioural and brain imaging measures of attention, inhibition and error processing.

Phase 4
Recruiting
Conditions
Study employs a commonly used ADHD medication (Clonidine) with healthy human adults (only) and examines changes in behaviours that are of relevance to ADHD (inhibition, error processing, selective attention)
Mental Health - Other mental health disorders
Registration Number
ACTRN12615000093583
Lead Sponsor
Professor Mark Bellgrove
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
26
Inclusion Criteria

healthy adult
Normal or corrected to normal vision

Exclusion Criteria

History of psychiatric illness
Currently on medication
Smoker
Regular recreational drug use

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
mean stop signal reaction time (SSRT) - a measure of response inhibition<br>[At approx 90-180 minutes following placebo vs Clonidine administration<br>];number of errors on error awareness task (EAT)<br>[Approximately 90-180 minutes following Placebo vs Clonidine administration];Mean asymmetry measure - spatial asymmetry task<br>[At approx 90-180 minutes following placebo vs Clonidine administration]
Secondary Outcome Measures
NameTimeMethod
amplitude of the Error positivity (Pe) - an electrophysiological (EEG) correlate of error awareness (see primary outcome 2) [At approx 90-180 minutes following placebo vs Clonidine administration];amplitude of the Error related negativity (ERN) - an electrophysiological (EEG) correlate of error processing (see primary outcome 2) [At approx 90-180 minutes following placebo vs Clonidine administration];EEG measure of (pre-target) alpha power spatial asymmetry (see primary outcome 3)[At approx 90-180 minutes following Placebo vs Clonidine administration]
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