Metaplasticity Clinical Trial
Official title:
Encoding a Motor Memory Through Metaplasticity
| Verified date | April 21, 2008 |
| Source | National Institutes of Health Clinical Center (CC) |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
This study will determine if applying electrical stimulation of the brain can influence
training to perform finger movements. The study may provide information that can be used to
design rehabilitation therapies for people who have lost the ability to move a part of their
body, such as an arm, leg, or hand following a stroke.
Healthy volunteers 18-50 years of age may be eligible for this study. Candidates are screened
with a medical history, physical examination, MRI (if one has not been done within the last
year), questionnaire to evaluate memory and attention and a pregnancy test for women who can
become pregnant.
Participants have the following tests and procedures in seven sessions over about 8 weeks:
- Questionnaires to test attention, fatigue and mood before, during and after each session
- Surface electromyography: Electrodes are filed with a conductive gel and taped to the
skin over one small hand muscle to measure the electrical activity of muscles.
- Transcranial magnetic stimulation: A wire coil is held on the scalp. A brief electrical
current passes through the coil to stimulate the brain. During the stimulation, the
subject may be asked to tense certain muscles slightly or perform other simple actions.
The stimulation may cause a twitch in muscles of the face, arm, or leg, and the subject
may hear a click and feel a pulling sensation on the skin under the coil.
- Transcranial direct stimulation (tDCS) before and during motor training: Small, wet
sponge electrodes are applied to the head - one above the eye and the other on the back
of the head. A small electrical current is passed between them. The subject may feel an
itching or tingling sensation under the electrodes or see light flashes.
- Motor learning under tDCS: tDCS is repeated while the subject performs the training
task. The training task consists of performing voluntary brisk thumb movements in a
direction opposite to TMS-induced movement directions, during 30 minutes. Training
blocks are in 10-minute segments and tDCS is applied during the first 20 minutes.
- Behavioral measurements: Evaluation of learned movement tasks.
| Status | Completed |
| Enrollment | 31 |
| Est. completion date | April 21, 2008 |
| Est. primary completion date | |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years to 50 Years |
| Eligibility |
- INCLUSION CRITERIA: - age between 18-50 years - able to perform tasks required by the study - willing and able to give consent - willing to make an eight-week commitment to the study - possibility of obtaining TMS-evoked thumb movements in a consistent direction at baseline EXCLUSION CRITERIA: - unable to perform the tasks - history of severe alcohol or drug abuse, psychiatric illness such as severe depression, poor motivational capacity, or severe language disturbances, particularly of receptive nature or with serious cognitive deficits (defined as equivalent to a mini-mental state exam score (MMSE) of 23 or less), or degenerative brain processes such as Alzheimer's disease - severe uncontrolled medical problems (e.g., cardiovascular disease, severe rheumatoid arthritis, active joint deformity of arthritic origin, active cancer or renal disease, any kind of end-stage pulmonary or cardiovascular disease, or a deteriorated condition due to age, uncontrolled epilepsy or others), more than moderate to severe microangiopathy, polyneuropathy, diabetes mellitus, or ischemic peripheral disease - problems with movement of the hands - receiving drugs acting primarily on the central nervous system, which lower the seizure threshold such as antipsychotic drugs (chlorpromazine, clozapine) or tricyclic antidepressants (for the TMS component) - pregnancy and during lactation - medical or technical contraindications to MRI procedures or devices producing artifacts that impair MRI signal (e.g., dental braces, pacemakers, implanted medication pumps, cochlear devices, neural stimulators, metal in the cranium, surgical clips, and other metal/magnetic implants, claustrophobia) |
| Country | Name | City | State |
|---|---|---|---|
| United States | National Institutes of Health Clinical Center, 9000 Rockville Pike | Bethesda | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| National Institute of Neurological Disorders and Stroke (NINDS) |
United States,
Siebner HR, Lang N, Rizzo V, Nitsche MA, Paulus W, Lemon RN, Rothwell JC. Preconditioning of low-frequency repetitive transcranial magnetic stimulation with transcranial direct current stimulation: evidence for homeostatic plasticity in the human motor cortex. J Neurosci. 2004 Mar 31;24(13):3379-85. — View Citation
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Unknown status |
NCT02263092 -
Effects of Transcranial Direct Current Stimulation Associated With Physical Exercise: a Metaplasticity Study
|
Phase 1/Phase 2 |