ADHD
Conditions
Keywords
ADHD, TMS, brain stimulation, clinical improvement
Brief summary
Objectives:The purpose of the study is to explore the efficacy and safety of HBLPADD Coil deep brain TMS in subjects with ADHD. Patient Population: The intention is to treat 40 patients diagnosed with ADHD. The patients will be of all racial, ethnic and gender categories, ranging from 18 to 65 years of age. Structure: The study is a randomized, prospective, 5 weeks, double blind study. Blinding: The treatment administrator and the study personnel and patients will be masked to the treatment being administrated. The study group will receive active dTMS treatment and the control group will receive an inactive, sham treatment
Interventions
DEVICEHBLPADD coil deep TMS
20 daily deep TMS treatment
DEVICESham
inactive treatment
Sponsors
Shalvata Mental Health Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Patients between the ages of 18-65(male and female). 2. Diagnosed as suffering from Attention-Deficit Hyperactivity Disorder according to the DSM IV. 3. Patients taking medication for ADHD will give their consent to stop those medication 48 before entering the study and throughout the daily treatments. 4. Gave informed consent for participation in the study. 5. If referred by the treating psychiatrist, he or she approves of the subjects participation in the study.
Exclusion criteria
1. Suffering from other diagnosis on axis 1. 2. antipsychotic treatment with stabilizers; medications from the Benzodiazepines group are allowed, if need be,to a maximum dosage of 2 mg lorazepam. 3. History of lack of tolerance to TMS. 4. Axis 2 diagnosis according to the DSM IV. 5. Substantial suicidal risk as judged by the treating psychiatrist or by an independent psychiatrist. 6. Attempted suicide in the past year. 7. High and not controlled blood pressure. 8. History of epilepsy, seizure, or hot spasm. 9. History of epilepsy or seizure in first degree relatives. 10. History of a significant head injury 11. History of metal in the head (outside the mouth space). 12. Known history of any metallic particles in the eye, implanted cardiac pacemaker or any intracardiac lines, implanted neurostimulators, surgical clips or any medical pumps. 13. Use of hearing aids for hearing loss. 14. History of frequent or severe headaches. 15. History of drug or alcohol abuse during the last year. 16. Inability to achieve satisfying level of communication with the subject. 17. Participation in current clinical study or clinical study within 30 days prior to this study 18. Patients declared as legally incompetent, with an appointed physical guardian and/or cannot sign informed consent due to cognitive incompetence. 19. Women - Pregnancy or not using a reliable method of birth control.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy will be examined by the change in the CAARS questionnaire from the baseline visit to the determination visit in the treatment group compared to the control group. | 5 weeks |
Secondary
| Measure | Time frame |
|---|---|
| clinical improvement as measured using Clinical global Impression (CGI). | 5 weeks |
Countries
Israel
Contacts
Primary ContactYechiel Levkovitz, MD
Outcome results
None listed