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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06030024
Other study ID # Attention
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2021
Est. completion date March 1, 2023

Study information

Verified date September 2023
Source University of Tehran
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
repetitive Transcranial Magnetic Stimulation
Magnetic pulses delivered to the Fz area of the brain in a low frequency (1 Hz) manner.

Locations

Country Name City State
Iran, Islamic Republic of National Brain Mapping Lab Tehran

Sponsors (1)

Lead Sponsor Collaborator
University of Tehran

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

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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