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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05206162
Other study ID # EC/2017/0780
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2, 2017
Est. completion date November 13, 2017

Study information

Verified date January 2022
Source University Hospital, Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess the effect of continuous (cTBS) and intermittent theta burst stimulation (iTBS) stimulation on motor cortex excitability using TMS-EEG. Based on prior literature, the investigators hypothesized that N100 amplitude would be differently modulated by these two modalities.


Description:

Each participant underwent three experimental sessions, at least one week apart in a cross-over design, assessing the effects of a single TBS train over the motor cortex on TMS-evoked potentials measured at the same location and resting-state EEG, immediately before and after the intervention. At each session a different type of TBS was applied (cTBS, iTBS or sham) in a randomized sequence. Subjects were uninformed about the expected effects of each intervention. Sham stimulation was achieved by adding a plastic spacer (25mm thickness) between coil and scalp, preventing effective cortical stimulation.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date November 13, 2017
Est. primary completion date November 13, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Age 18-65 years - Male - Right handed subjects - IQ > 70 - Healthy participants, as determined by history, clinical investigation and investigator's judgment - No history of central nervous system condition - No chronic intake of neurotropic drugs - TMS Safety Screening questionnaire and informed consent signed Exclusion Criteria: - Pregnancy, short-term birth wish or childbearing age without adequate birth control - Intracranial metal hardware (excluding dental filling): surgical clips, shrapnell, electrodes under the stimulation area - Presence of pacemaker, implantable cardioverter-defibrillator (ICD), permanent medication pumps, cochlear implants or deep brain stimulation (DBS)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
theta burst stimulation
TBS over the left motor hotspot, delivered at 80% of resting motor threshold (RMT), according to the Huang et al. protocol, consisting of bursts of stimuli that are presented every 200ms (5Hz), with bursts consisting of 3 stimuli at 50 Hz. A total of 600 pulses are delivered.

Locations

Country Name City State
Belgium University Hospital Ghent Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary TBS-induced modulation of single-pulse TMS-evoked EEG responses (TEPs) - peak latency/amplitude of TEP components at Cz measurement takes place immediate before and after TBS stimulation train
Primary TBS-induced modulation of single-pulse TMS-evoked EEG responses (TEPs) - Local Mean Field Power (LMFP) across a region of interest (ROI) measurement takes place immediate before and after TBS stimulation train
Primary TBS-induced modulation of single-pulse TMS-evoked EEG responses (TEPs) - divergence index (DI) across all EEG channels measurement takes place immediate before and after TBS stimulation train
Secondary TBS-induced modulation of paired-pulse TMS-evoked EEG responses (TEPs) measurement takes place immediate before and after TBS stimulation train
Secondary TBS-induced modulation of resting-state EEG measurement takes place immediate before and after a single TBS stimulation train
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