Attention Deficit Hyperactivity Disorder Clinical Trial
Official title:
Role of Transcranial Direct Current Stimulation (tDCS) in Patients With Attention Deficit Hyperactivity Disorder (ADHD)
The purpose of this study is to determine whether transcranial direct current stimulation
(tDCS) is effective in the treatment attention deficit hyperactivity disorder (ADHD).
Randomized, double-blind Controlled Clinical Trial
Subjects Adults (between 18 and 59 years of age) with ADHD who meet the inclusion criteria
and who agree to participate in the study Will recruit from advertisements and clinical
referrals to a PRODAH
Active tDCS Anode - right DLPFC Cathode - left DLPFC Electric current is 2mA - Current is
applied for 20 min
Sham tDCS Same assembly is used Current is applied for 30 sec
Both groups 5 stimulation sessions on consecutive days
Following tools at Baseline, 1st week, 2 st week, 3st week and 4st week Adult ADHD
Self-Report Scale (ASRS) SDS - Sheehan Disability Scale CGI - Clinical Global Impression
Randomized, double-blind Controlled Clinical Trial
Subjects Adults (between 18 and 59 years of age) with ADHD who meet the inclusion criteria
and who agree to participate in the study Will recruit from advertisements and clinical
referrals to a PRODAH
Active tDCS Anode - right DLPFC Cathode - left DLPFC Electric current is 2mA - Current is
applied for 20 min
Sham tDCS Same assembly is used Current is applied for 30 sec
Both groups 5 stimulation sessions on consecutive days
Following tools at Baseline, 1st week, 2 st week, 3st week and 4st week Adult ADHD
Self-Report Scale (ASRS) SDS - Sheehan Disability Scale CGI - Clinical Global Impression
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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