MedPath

T-mult: exploring the impact of TMS induced virtual lesions on the multimodal brain network and cognitio

Recruiting
Conditions
not applicable
10029305
cognitief functioneren
Registration Number
NL-OMON53939
Lead Sponsor
Vrije Universiteit Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

* Age between 20 and 65 years old
* Native Dutch speaker
* Able to provide written informed consent.

Exclusion Criteria

* Current diagnosis of neurological or psychiatric disease (including traumatic
head injury)
* Current and regular use of centrally acting drugs (recreational or
prescribed, including analgesics), including use of alcohol ~8 hours prior to
an appointment
* Presence of any contraindications for MRI, MEG, or TMS (including
resting-motor threshold >75% of maximum stimulator output or no useful
motor-evoked potential elicitable)
* Previous rTMS treatment.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary effect of rTMS will be assessed through the change in performance<br /><br>on a neuropsychological test measuring executive functioning in the domain of<br /><br>executive functioning pre- and post-intervention. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondarily, changes in network organization will be characterised by<br /><br>(multimodal) neuroimaging pre- and post-treatment. Pre-treatment imaging will<br /><br>include magnetoencephalography (MEG), diffusion MRI (dMRI), task-based<br /><br>functional MRI (tbfMRI), and resting state fMRI (rsfMRI); post-treatment<br /><br>imaging will include only tbfMRI. </p><br>
© Copyright 2025. All Rights Reserved by MedPath