Status:
UNKNOWN
Deep Transcranial Magnetic Stimulation (DTMS) as a Treatment for Attention Deficit Hyperactivity Disorder (ADHD) in Adults
Lead Sponsor:
Brainsway
Conditions:
Attention Deficit Hyperactivity Disorder
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
Brief Summary
The aim of the study is to assess the effect of left or right high-frequency DTMS on ADHD symptoms, cognitive performance and decision-making ability of ADHD adults, and to compare this to the effect ...
Detailed Description
Attention deficit disorder in adults may be due to hypoactivity of prefrontal areas of the brain. Increasing the activity of these areas may help improve symptoms in many of these patients. In additio...
Eligibility Criteria
Inclusion
- Men and women aged 18-65.
- Appropriate diagnosis of ADHD according to DSM-IV criteria:
- o DSM-IV criteria require not only that the ADHD symptoms be present now (self-report), but also to have been present in childhood (self-report)
- Subjects taking medications for attention deficit disorder will give their consent to stop the drugs from a week before the start of participation in the study, and during the daily treatment phase (four weeks total); subjects also will be asked not to take these medications 24 hours before participation in the review meetings (4 and 8 weeks after the end of the daily treatment phase).
- Subjects have given their written and oral consent to participate in research.
Exclusion
- Any DSM-IV Axis I psychiatric disorder.
- Use of antipsychotic stabilizers; other than benzodiazepines if necessary to a daily dosage equivalent to 2 mg Lorazepam.
- History of lack of tolerance to TMS.
- Diagnosis of severe DSM-IV personality disorder.
- Current suicidal tendency.
- Uncontrolled high blood pressure
- History of epilepsy, seizures or fever convulsions.
- History of epilepsy or convulsions in first-degree relatives.
- A history of head injury or a stroke which caused deficits.
- History of metal in the head (outside the oral cavity).
- History of plastic or metal implants, including metallic particles in the eye, pacemaker, implanted hearing aid devices, use of neurostimulators, or any medical pump.
- A history of drug or alcohol misuse.
- People who lack judgment or are unable to communicate with the experimenters.
- Participation in any other medical research during the three months prior to the time of this experiment.
- Subject's inability to sign a consent form.
- Pregnancy, or not using contraception.
Key Trial Info
Start Date :
July 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2020
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT01196910
Start Date
July 1 2011
End Date
September 1 2020
Last Update
July 14 2020
Active Locations (1)
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1
Tel-Aviv Sourasky Medical Center
Tel Aviv, Israel