Trial to Evaluate the Efficacy of the HLPFC Coil Deep Transcranial Magnetic Stimulation System in Treating Attention Deficit and Hyperactivity Disorder (ADHD) in Adults
November 26, 2012 updated by: Soroka University Medical Center
The aim of the study is to investigate the efficacy of trans-cranial magnetic stimulation in treating attention deficit disorder in adults.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hadar Shalev, MD
- Phone Number: 97286400353
- Email: shalev@bgu.ac.il
Study Locations
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-
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Beer-Sheva, Israel
- Ben-Gurion University
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Contact:
- Hadar Shalev, MD
- Phone Number: 97286400353
- Email: shalev@bgu.ac.il
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18-65 years
- ADD/ADHD
Exclusion Criteria:
- any DSM-IV psychiatric disorder except ADD/ADHD
- use of psychoactive medications
- Epilepsy
- brain injury
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Sham Comparator: control
control-sham
|
Other Names:
|
|
Active Comparator: Deep TMS PFC Lt
Deep TMS PFC left
|
Other Names:
|
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Active Comparator: DEEP TMS PFC Rt
|
Other Names:
|
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Active Comparator: Superficial TMS PFC Lt
|
Other Names:
|
|
Active Comparator: superficial TMS PFC Rt
|
Other Names:
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
November 1, 2012
Primary Completion (Anticipated)
August 1, 2015
Study Registration Dates
First Submitted
September 20, 2012
First Submitted That Met QC Criteria
November 26, 2012
First Posted (Estimate)
November 29, 2012
Study Record Updates
Last Update Posted (Estimate)
November 29, 2012
Last Update Submitted That Met QC Criteria
November 26, 2012
Last Verified
November 1, 2012
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- sor010912ctil
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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