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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03480737
Other study ID # BradleyH
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2019
Est. completion date March 30, 2021

Study information

Verified date November 2019
Source Bradley Hospital
Contact Brian Kavanaugh, PsyD
Phone 401 432 1359
Email brian_Kavanaugh@brown.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Executive functioning (EF) deficits are a core, transdiagnostic feature of psychopathology and one of the strongest predictors of clinical and functional outcomes, yet there remains a dearth of treatments available for EF deficits. EF is a collection of cognitive control processes that includes working memory (i.e., maintain/manipulate data not perceptually present), inhibition (i.e., inhibit/control of attention, thoughts, behaviors) and flexibility (i.e., shift flexibly between tasks/sets). These EF subdomains are subserved by a network (i.e., cognitive control network) of frontal (e.g., dorsolateral prefrontal cortex [DLPFC]), parietal and subcortical regions, with hypoactivation in such regions often underlying EF deficits. There is a recent call in psychiatry to develop experimental therapeutics that target anomalous neural systems underlying symptomology. Repetitive transcranial magnetic stimulation (rTMS) is a therapeutic, non-invasive method of cortical excitability modulation. High frequency rTMS to the left DPLFC has an activating effect on the cognitive control network, with initial research in adults finding a subsequent enhancing effect on working memory, inhibition, and flexibility. rTMS represents a very promising potential tool to target EF deficits in psychopathology.


Recruitment information / eligibility

Status Recruiting
Enrollment 25
Est. completion date March 30, 2021
Est. primary completion date January 30, 2021
Accepts healthy volunteers No
Gender All
Age group 13 Years to 17 Years
Eligibility Inclusion Criteria:

1. Ability to provide assent and have parent provide parental permission

2. English fluency

3. 13-17 years

4. List Sorting Test (NIH Toolbox) performance: Greater than 1.0 standard deviation (SD) below normative mean

5. Parent rating on BRIEF-2 Working Memory: Greater than 1.0 SD above normative mean

6. IQ > 80

7. Clinical diagnosis of attention deficit hyperactivity disorder (ADHD): predominantly inattentive type, predominantly hyperactive/impulsive type, combined type, or unspecified type. Diagnostic criteria will be confirmed with NICHQ Vanderbilt Assessment Scales-Parent.

Exclusion Criteria:

Participants will be screened to exclude individuals with neurological or medical conditions that might confound the results, as well as to exclude participants in whom rTMS might result in increased risk of side effects or complications. Common TMS contraindications include metallic hardware in the body, cardiac pacemaker, patients with an implanted medication pumps or an intracardiac line, or prescription of medications known to lower seizure threshold. This accounts for the majority of the exclusion criteria listed:

1. Intracranial pathology from a known genetic disorder (e.g., NF1, tuberous sclerosis) or from acquired neurologic disease (e.g. stroke, tumor), cerebral palsy, history of severe head injury, or significant dysmorphology

2. History of fainting spells of unknown or undetermined etiology that might constitute seizures

3. History of seizures, diagnosis of epilepsy, or immediate (1st degree relative) family history epilepsy

4. Any progressive (e.g., neurodegenerative) neurological disorder

5. Chronic (particularly) uncontrolled medical conditions that may cause a medical emergency in case of a provoked seizure (cardiac malformation, cardiac dysrhythmia, asthma, etc.)

6. Contraindicated metal implants in the head, brain or spinal cord (excluding dental implants or fillings)

7. Pacemaker

8. Implanted medication pump

9. Vagal nerve stimulator

10. Deep brain stimulator

11. TENS unit (unless removed completely for the study)

12. Ventriculo-peritoneal shunt

13. Signs of increased intracranial pressure

14. Intracranial lesion (including incidental finding on MRI)

15. History of head injury resulting in prolonged loss of consciousness

16. Substance abuse or dependence within past six months (i.e., DSM-5 substance use disorder criteria met)

17. Chronic treatment with prescription medications that decrease cortical seizure threshold

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Magstim Super Rapid2 stimulator, 10 Hz condition
10 Hz (2,000 pulses) at left DLPFC
Magstim Super Rapid2 stimulator, Sham condition
sham
Magstim Super Rapid2 stimulator, iTBS condition
50 Hz, iTBS (600 pulses) at left DLPFC

Locations

Country Name City State
United States E. P. Bradley Hospital East Providence Rhode Island

Sponsors (3)

Lead Sponsor Collaborator
Bradley Hospital Rhode Island Foundation, Thrasher Research Fund

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Compared to sham condition, activation of the left DLPFC prior to EF training will temporarily increase working memory performance as measured by the Sternberg Spatial Working Memory Test The SWMT is a performance-based neuropsychological test of working memory Task performance will be measured immediately prior to and following the active and sham rTMS/EF training sessions.
Secondary Compared to sham condition, activation of the left DLPFC prior to EF training will temporarily increase fronto-parietal gamma power and theta-gamma coupling during working memory demands. EEG will be measured during SWMT immediately prior to and following the active and sham rTMS/EF training sessions.