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Motor Function of Healthy PhysiologyEarly Phase 1NCT00453505

Modulation of Motor Function by Stimulation of the Central and Peripheral Nervous System

A Early Phase 1 study testing TMS, tDCS and tACS in people with Motor Function of Healthy Physiology, run by National Institute of Neurological Disorders and Stroke (NINDS) at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

Objectives When a stroke damages the part of the brain that controls movement, people have weakness and difficulty using their hand. There is often some improvement, but many people have permanent disability in using the affected hand. Read more about this study

Who is it for?
Ages 18 to 120 years
Conditions the study is for
Motor Function of Healthy Physiology
What is being tested?
TMS, tDCS and tACS
Type of treatment
Medical device
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
976 participants
Where
1 siteUnited States
Study dates
14 Jan 2007to 20 Dec 2019
Phase
Early Phase 1

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 120 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 and older
  • Willingness and ability to give consent
  • Normal neurological examination
  • Clearly dominant handedness (right or left) as assessed by Handedness scales

Who cannot join

  • Any severe or progressive neurological disorder or severe medical condition, or history of seizures
  • Chronic use of medications acting primarily on the central nervous system, which lower the seizure threshold or significantly alter cortical excitability such as antipsychotic drugs (chlorpromazine, clozapine), tricyclic or other antidepressants, or prescription stimulants.
  • Pacemakers or other implanted electrical devices, brain stimulators, some types of dental implants, aneurysm clips (metal clips on the wall of a large artery), metallic prostheses (including metal pins and rods, heart valves, and cochlear implants), permanent eyeliner, implanted delivery pump, or shrapnel fragments
  • Diagnosis of drug dependence made by a health care provider (ICD-9-CM code 304)
  • Staff from our section

Trial locations and contacts

1 site in 1 country.

United States1 site
  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892

Other trials in United States

About this study

Objectives

When a stroke damages the part of the brain that controls movement, people have weakness and difficulty using their hand. There is often some improvement, but many people have permanent disability in using the affected hand. Our previous research has shown that if we stimulate the nerves or the brain, we can temporarily improve how fast people with and without strokes can move their hands. But improvement is very slight and doesn t last long.

Read more

In this study, we are trying to see if different combinations of brain, skin and nerve stimulation might cause more improvement in motor function or learning. For this study, we will only include healthy people who have not had a stroke. We will use one or more types of electrical and magnetic stimulation of skin, nerves and the brain, or recording of behavior or brain activity alone without stimulation.

Study Population

Up to 1500 healthy volunteers, age 18 and older.

What will volunteers do in this study

Visits may include the following procedures:

Electromyography (EMG) which measures electrical activity of muscles.

Transcranial Magnetic Stimulation (TMS) where a wire coil is placed on the scalp, and brief electrical current creates a magnetic pulse that temporarily affect brain activity. This may feel like a pulling sensation where the coil is placed, and may result in twitches in the face, arm, or leg.

Transcranial direct current stimulation (tDCS), a technique in which a very weak electrical current is applied to the head in order to stimulate the brain.

Nerve Stimulation, where sticky pads or small metal disk electrodes attached to wires onto the skin to record muscle and nerve activity.

Magnetic resonance imaging (MRI) which uses a strong magnetic field and radio waves to take pictures of the brain. Some MRIs the volunteers are asked to lie still, and in others are asked to do various movements.

Magnetic resonance spectroscopy (MRS) uses a strong magnetic field and radio waves to take pictures of various chemicals in the brain using an MRI scanner.

Electroencephalogram (EEG) to record the electrical activity of the brain ( brain waves ).

Magnetoencephalography (MEG) records small magnetic field changes from brain activity.

Eye movement recordings

Behavioral Tests

Questionnaires

Pregnancy test (for those capable of getting pregnant)

How long is the study?

Volunteers in this study may have multiple visits. Each visit may last up to 8 hours. The number of visits we depend on the data the researchers want to collect. You may be asked to come back for visits over multiple years (up to 20 years). Taking part in this study is completely voluntary. People who volunteer to be in the study can change their mind at anytime.

Read the detailed description

Objectives

Noninvasive stimulation of the central and peripheral nervous system, including transcranial magnetic stimulation (TMS), transcranial direct and alternating current stimulation (tDCS and tACS, respectively) and cutaneous/peripheral nerve stimulation (C/PNS) alone or paired with TMS (paired associative stimulation, PAS), has been increasingly used in the investigation of cortical plasticity and as a possible adjuvant strategy in neurorehabilitation. It has been shown that TMS, tDCS, tACS and C/PNS can modulate motor function in healthy volunteers, as well as in patients with neurological disorders such as stroke.

One fundamental problem is that the optimal parameters of stimulation to modulate motor function by all of these techniques are not known. The purpose of this protocol has been to explore within safe guidelines, the effects of different stimulation parameters on motor cortical function, on oscillatory brain dynamics measured with magnetoencephalography (MEG) and electroencephalography (EEG), on eye movements, and on fMRI activation. In addition, this protocol was used to train new fellows coming to NINDS Human Cortical Physiology Section (HCPS) in the use of TMS, tDCS, tACS and C/PNS techniques.

We expected that information emerging from these studies would allow us to 1) optimize experimental protocols or stimulation parameters to collect pilot data in healthy volunteers for future patient-oriented hypothesis-driven protocols, 2) to collect pilot data for power analysis for future patient-oriented hypothesis driven protocols, and 3) to train new fellows in the use of these different methods.

As instructed, we had stopped recruitment under this protocol at the time we were informed by the NIH IRB that they determined this to be a thematic protocol (August 6, 2019). The four specific aims addressed under this protocol are:

  1. Aim 1. To identify resting behavioral and physiological substrates for neuromodulation of motor behavior
  2. Aim 2. To identify task-dependent behavioral and physiological substrates for neuromodulation of motor behavior
  3. Aim 3. To understand variability, rigor or/and reproducibility of brain stimulation effects.

As instructed, the purpose of this amendment is to request authorization to proceed with data analysis and publication. No new experiments will be carried out under this protocol.

Study Population

Up to 1500 healthy volunteers, age 18 and older.

Design

No new experiments will be carried out under this protocol. Previously, healthy volunteers received one or more of the following types of stimulation alone or in combination: (1) single- and paired-pulse TMS with inter-stimulus intervals of greater than 1s and up to 20s and intensities of up to 100% of stimulator output; (2) 1 Hz TMS for up to 30mins and up to 115% of resting motor threshold (RMT) intensity; (3) tDCS applied at an intensity of up to 4 mA for a duration of up to 60mins, as long the total charge does not exceed 7.2 C; (4) tACS applied at a peak-to-peak intensity of up to 4 mA for a duration of up to 60 minutes, as long the total charge does not exceed 7.2 C; (5) C/PNS applied alone with intensities below 130% of the peripherally-elicited-motor-threshold for up to 2 hours, or intensities up to 300% of sensory threshold when C/PNS is paired with TMS. All of these parameters of stimulation and procedures have safely been used as previously reported in the literature. Sham stimulations were delivered for each modality as scientifically needed. Some sessions included recording of behavior or brain activity (such as behavioral testing, MRI, and MEG) if brain stimulation targets were unknown. This information was used to inform the design of brain stimulation protocols.

Each subject was able to participate in up to one experimental session per day, and up to 20 total sessions over a twenty year period under this protocol. A single session lasted no longer than 8 hours. Appropriate rest breaks and meal breaks occured during long sessions. CTDB was used to track the number of sessions per subject to ensure they did not exceed 20 sessions. Protocol AIs were responsible for entering the subjects/sessions into CTDB.

We previously tested the effects of different forms of stimulation on motor cortical excitability, cognitive and motor behavioral tasks, and brain state measures derived from neuroimaging data (i.e. - MRI, fMRI, MEG and EEG). Stimulation was be applied before, after, or during physiological (i.e. motor evoked potentials, M-wave, F-wave, or H-Reflexes), neuroimaging or behavioral measures.

Outcome Measures

No new outcome measures are proposed. Changes in motor cortical excitability were previously measured as the change in the average peak-to-peak amplitude of a motor evoked potential (MEP) as measured with EMG. Neuroimaging measures included changes in oscillatory brain activity power as measured with EEG or MEG, changes in BOLD fMRI activation or changes in functional connectivity (i.e. covarying fluctuations in BOLD or spectral power across the brain). Behavioral outcome measures focused on changes in performance as a function of learning, or as a function of applied brain stimulation.

Being tested
TMS, tDCS, tACS, CPNS
Keywords
Transcranial Direct Current Stimulation, Transcranial Magnetic Stimulation, Peripheral Nerve Stimulation, Primary Motor Cortex, Corticomotor Excitability, Healthy Volunteer, HV

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TMSDevice

    <=1 Hz TMS for up to 30mins and up to 115% of resting motor threshold intensity (MT).

  • tDCSDevice

    tDCS up to 2 mA for up to 60mins.

  • tACSDevice

    tACS up to 1 mA for up to 10 minutes.

  • CPNSDevice

    CPNS alone with intensities below 130% of the peripherally-elicited-motor-threshold for up to 2 hours.

Study groups in NCT00453505
Study groupRoleWhat they receive
1ExperimentalHealthy Volunteers
Receives: Device: TMS
1aSham comparatorHealthy Volunteers
Receives: Device: TMS
2ExperimentalHealthy Volunteers
Receives: Device: tDCS
2aSham comparatorHealthy Volunteers
Receives: Device: tDCS
3ExperimentalHealthy Volunteers
Receives: Device: tACS
3aSham comparatorHealthy Volunteers
Receives: Device: tACS
4ExperimentalHealthy Volunteers
Receives: Device: CPNS
4aSham comparatorHealthy Volunteers
Receives: Device: CPNS

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. To identify task-dependent behavioral and physiological substrates for neuromodulation of motor behavior Aim

    in data analysis

    Measured: in data analysis

  2. To understand variability, rigor or/and reproducibility of brain stimulation effects.

    in data analysis

    Measured: in data analysis

  3. To identify resting behavioral and physiological substrates for neuromodulation of motor behavior Aim

    in data analysis

    Measured: in data analysis

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Mar 2007 (estimated)
  2. Study start14 Jan 2007
  3. Primary completion8 Nov 2019
  4. Study completion20 Dec 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Early Phase 1
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
976 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00453505
Sponsor's protocol ID
070122
Other IDs
07-N-0122
Status last verified
28 Aug 2026
First submitted
28 Mar 2007
Last updated
28 Sep 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Wassermann EM. Risk and safety of repetitive transcranial magnetic stimulation: report and suggested guidelines from the International Workshop on the Safety of Repetitive Transcranial Magnetic Stimulation, June 5-7, 1996. Electroencephalogr Clin Neurophysiol. 1998 Jan;108(1):1-16. doi: 10.1016/s0168-5597(97)00096-8.

    PubMed 9474057
  • Pascual-Leone A, Valls-Sole J, Wassermann EM, Hallett M. Responses to rapid-rate transcranial magnetic stimulation of the human motor cortex. Brain. 1994 Aug;117 ( Pt 4):847-58. doi: 10.1093/brain/117.4.847.

    PubMed 7922470
  • Muellbacher W, Ziemann U, Boroojerdi B, Hallett M. Effects of low-frequency transcranial magnetic stimulation on motor excitability and basic motor behavior. Clin Neurophysiol. 2000 Jun;111(6):1002-7. doi: 10.1016/s1388-2457(00)00284-4.

    PubMed 10825706

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