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Evaluation of the Effect of rTMS on Attention in Adults Diagnosed With Attention-Deficit Hyperactivity Disorder (ADHD)

Not Applicable
Conditions
Attention Deficit Hyperactivity Disorder
Registration Number
NCT00825708
Lead Sponsor
Shalvata Mental Health Center
Brief Summary

The aim of the study is to evaluate the immediate effect of rTMS on attention in adults diagnosed with ADHD. the design is a double blind sham controlled crossover study.

Detailed Description

The subjects were randomly assigned to two groups. group 1 starts with the real rTMS session followed within one week with a sham session. group 2 starts with a sham session and within one week recieve a real session. the subjects go through a neurocognitive evaluation before and after rTMS sessions and a clinical evaluation questionnaire modified for attention.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • age 18-65
  • diagnosis of ADHD according to DSM IV criteria
Exclusion Criteria
  • other axis I diagnosis
  • risk factors for seizure

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
PANNAS questionnaire modified for attentionwithin one hour of the rTMS session
Secondary Outcome Measures
NameTimeMethod
the CANTAB neurocognitive batterywithin 2 hours of the stimulation

Trial Locations

Locations (1)

Shalvata MHC, cognitive and emotion lab

🇮🇱

Hod Hasharon, Israel

Shalvata MHC, cognitive and emotion lab
🇮🇱Hod Hasharon, Israel
Yuval Bloch, MD
Principal Investigator
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