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The Therapeutic Role of rTMS in Children with ADHD a Pilot Study

Phase 2
Conditions
Mental and Behavioural Disorders
Registration Number
PACTR202110558451583
Lead Sponsor
FACULTY OF MEDCINE AIN SHAMS UNIVERSITY
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Patients diagnosed with ADHD according to DSM IV
Age ranges 7-12 years old
All patients will be on the same type of medications throughout the duration of the study (Atomoxetine 1.2 mg/kg/day)

Exclusion Criteria

Factors that might increase the risk of seizure with TMS such as a history of a seizure disorder, febrile seizures during childhood, known brain lesions, or a history of major head trauma involving loss of consciousness for more than 5 minutes.

Specific contraindications to magnetic stimulation such as any metallic object implanted in the skull (with the exception of oral dental devices), an implanted medication pump or cochlear implant, implanted intra-cardiac lines or pacemaker.

Comorbid diagnosis of autism spectrum disorder, bipolar disorder, obsessive-compulsive disorder, conduct disorder, Tourette disorder or other tic disorders, schizophrenia, schizoaffective disorder, or any other psychotic disorder.

Any other neurological disorders.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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