NCT01041300

Brief Summary

Our aim is to Test the influence of a new multichanel Transcranial Magnetic Stimulation stimulator (Multiway) on motor excitation, in comparision to a wildly used Magstim Super Rapid 2 single channel stimulator. Each of the 20 Healthy subjects that are inticipated to inrole to the study wiil undergo 6 simple procedures which are designed to compare the motor threshold obtained by diffrent combination of TMs coils (figure 8, double cone coil,H coil array) and stimulators (Multiway, Super Rapid 2). The entire length of the procedures is about 4 hours and all subjects will be paid for their participation in the study. Our main hypothesis is that the motor threshold obtained by the multichanel stimulator will be significtly lower then the single chanel stimulator.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
34

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Jan 2010

Typical duration for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 22, 2009

Completed
9 days until next milestone

First Posted

Study publicly available on registry

December 31, 2009

Completed
1 day until next milestone

Study Start

First participant enrolled

January 1, 2010

Completed
1.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2011

Completed
Last Updated

January 5, 2012

Status Verified

January 1, 2012

Enrollment Period

1.7 years

First QC Date

December 22, 2009

Last Update Submit

January 4, 2012

Conditions

Keywords

Transcranial Magnetic StimulationTMSMotor ThreasholdMultiwayMagstim Rapid 2Abductor policis brevisFigure 8 coilDouble cone coilCircular coilBrainswayHealthy participants.

Outcome Measures

Primary Outcomes (5)

  • Comparison between abductor policis brevis (APB) motor thresholds obtained with figure-8 using Magstim and Brainsway stimulators, for the same subjects

    one day

  • Comparison between the total power required for APB motor thresholds obtained with figure-8 Coil operated with a single channel, and circular coils operated with several channels of the Brainsway stimulator, for the same subjects.

    one day

  • Comparison between the total power required for leg motor thresholds obtained with Double Cone Coil operated with a single channel, and circular coils operated with several channels of the Brainsway stimulator, for the same subjects.

    one day

  • Comparison between the latency times for leg motor thresholds obtained with Double Cone Coil operated with a single channel, and circular coils operated with several channels of the Brainsway stimulator, for the same subjects.

    one day

  • Comparison between the motor thresholds and motor evoked potentials (MEPs) obtained with various combinations of relative intensities of pulses produced by several channels of the multi-channel Brainsway stimulator.

    one day

Interventions

Duration: Time is takes to find motor thresholds obtained with figure-8 coil using Magstim Rapid2 Stimulator (Estimated at 15 minutes). Total Duration of device: 15 minutes

Finding motor thresholds using the figure-8 coil and the Brainsway Multi-channel Stimulator (Estimated at 15 minutes). Finding motor threshold of leg obtained with Double Cone coil using the Brainsway Multi-channel Stimulator (Estimated at 15 minutes). Finding motor threshold of leg obtained with circular coils using the Brainsway Multi-channel Stimulator (Estimated at 15 minutes). Finding motor threshold of thumb obtained with circular coils on multiple channels using the Brainsway Multi-channel Stimulator (Estimated at 15 minutes). Finding motor thresholds of multiple channels using the Brainsway Multi-channel Stimulator (Estimated at 1 hour). Finding specificity of the motor thresholds of multiple channels using the Brainsway Multi-channel Stimulator (Estimated at 30 minutes). Total Duration with Device: 2 hours and 30 minutes

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Individuals between the ages of 18-65
  • Right handed individuals
  • Individual provides Negative responses to the questions on the safety questionnaire completed prior to TMS treatment.
  • Individual gave both written and verbal consent to participation in the study.

You may not qualify if:

  • Individual suffers from an Axis I disorder, as diagnosed in a Clinical interview with a Psychiatrist.
  • Individual suffers from an Axis II disorder, as diagnosed in a Clinical interview with a Psychiatrist.
  • Individual has a history of high blood pressure.
  • Individual has a history of epilepsy, epileptic seizure, or febrile seizures.
  • Individual has family members with a history of epilepsy, epileptic seizures or febrile seizures.
  • Individual has a history of head injury.
  • Individual has any metal implants in head (except for dental implants)
  • Individual has history of surgery, including metal implants or individual has a known history of metal particals in the eye, heart pumps, neurostimulator use, or any other medical pump.
  • Individual has a history of migrane.
  • Individual has a history of hearing problems or deafness.
  • Individual has a hisotry of hearing aids or implants.
  • Individual has a hisotry of drug or alcohol addiction.
  • Individual is pregnant or is sexually active and not using contraception.
  • Individual is to difficult to contact.
  • Indicidual has a legal gaurdian.
  • +2 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shalvata Mental Health Center

Hod HaSharon, Israel

Location

Study Officials

  • Eiran V Harel, MD

    Shalvata Mental Health Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 22, 2009

First Posted

December 31, 2009

Study Start

January 1, 2010

Primary Completion

October 1, 2011

Study Completion

October 1, 2011

Last Updated

January 5, 2012

Record last verified: 2012-01

Locations