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

S

Shalvata Mental Health Center

Status

Unknown

Conditions

Attention Deficit Hyperactivity Disorder

Treatments

Device: rTMS
Device: shamTMS

Study type

Interventional

Funder types

Other

Identifiers

NCT00825708
SH20107

Details and patient eligibility

About

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.

Full 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.

Enrollment

20 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 18-65
  • diagnosis of ADHD according to DSM IV criteria

Exclusion criteria

  • other axis I diagnosis
  • risk factors for seizure

Trial design

20 participants in 2 patient groups

rTMS
Active Comparator group
Description:
rTMS session
Treatment:
Device: rTMS
SHAM
Sham Comparator group
Description:
sham session
Treatment:
Device: shamTMS

Trial contacts and locations

1

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Central trial contact

Eiran V Harel, MD

Data sourced from clinicaltrials.gov

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