ADHD Clinical Trial
Official title:
An Open-lable Investigation of the Effect of rTMS on Attention in an Adult Sample Suffering From ADD
Verified date | September 2023 |
Source | University of Tehran |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of the current open-lable study was to use low-frequency repetitive transcranial magnetic stimulation (rTMS) to improve the attention deficits in a sample of adult patients suffering from attention deficit disorder. Participants received 10 sessions of rTMS over Fz (located using the EEG 10-20 international system) and underwent assessments of their attentional capacity using the gradCPT task in an fMRI scanner, before and after the intervention. Other behavioral assessments of their attention symptoms have also been conducted.
Status | Completed |
Enrollment | 10 |
Est. completion date | March 1, 2023 |
Est. primary completion date | February 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Normal intelligence level (>90) - Diagnosis of ADD by a psychiatrist using the ADHD-RS-IV with Adult Prompts Exclusion Criteria: - Scores of 21 or more on BDI and/or BAI - History of head trauma - History of a major psychological or neurological condition - Presence of metal in the head - History of seizures - Serious cardiovascular disease - Use of medications with an impact on cognitive functions during the treatment window (patients with a constant and stable dose were included) - Recent use of alcohol or substance abuse |
Country | Name | City | State |
---|---|---|---|
Iran, Islamic Republic of | National Brain Mapping Lab | Tehran |
Lead Sponsor | Collaborator |
---|---|
University of Tehran |
Iran, Islamic Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in performance | Shortened version (4 min) of the continuous go/no-go task: gradual-onset continuous performance task (gradCPT) | Up to 10 days, i.e., before and after the completion of the 10 sessions of rTMS | |
Secondary | Change in self-report attention scores | The 6-item ASRS-V1.1 Adult ADHD Self-Report | Baseline, after 5 days of stimulation, after 10 days of stimulation; Range= 0-6; Higher scores represent worse outcome | |
Secondary | Change in investigator-rated attention scores | Investigator-Rated Attention-Deficit Hyperactivity Disorder (ADHD) Rating Scale-IV (I-ADHD RS-IV) with adult prompts | Baseline, after 5 days of stimulation, after 10 days of stimulation; Range:0 - 54; Higher scores represent worse outcome |
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