Healthy Clinical Trial
Official title:
Motor Learning: Behavioral and Physiologic Studies in Normal Volunteers and Stroke Patients
This study will try to elucidate learning processes associated with motor training in the
weak arm of stroke patients compared with healthy controls. Results from previous clinical
trials indicate that training may enhance motor function in healthy volunteers, and perhaps
also in stroke patients, even more than 1 year after the stroke. Normal, healthy volunteers
and stroke patients 18 years of age and older may be eligible for this study.
Study subjects will have a physical examination and participate in 6 additional clinic
visits-training and testing sessions on study days 1, 2, 3, 4 and 5, and a final testing
session on day 12. During these sessions, they will perform a series of motor tasks,
including writing, picking up objects, turning cards, stacking checkers and moving cans,
which will be timed and videotaped. Each session will be divided into blocks of 10 trials
for each task, separated by 2-minute rest periods.
Before and after training on days 1, 2, 5 and 12, subjects will have transcranial magnetic
stimulation (TMS) to determine brain changes associated with learning a motor task. For this
procedure, the patient is seated in a comfortable chair, and an insulated wire coil is
placed on the scalp or skin. A brief electrical current is passed through the coil, creating
a magnetic pulse that stimulates the brain. These pulses generate very small electrical
currents in the brain cortex, briefly disrupting the function of the brain cells in the
stimulated area. The stimulation may cause muscle twitching or tingling in the scalp, face,
or limb. During the stimulation, the subject may be asked to slightly tense certain muscles
or perform other simple actions.
Electrical nerve stimulation and electromyography will be done to record muscle responses to
stimulation. A nerve is stimulated by placing wires on the skin over the nerve and passing a
brief electrical current between the wires. Electromyography involves taping metal
electrodes to the skin over the muscle.
Before and after each session, subjects' muscle strength will be tested with a pinch gauge.
They will also be asked to make a mark on a line drawn on paper, to rate their test
performance and levels of attentiveness and fatigue.
| Status | Completed |
| Enrollment | 78 |
| Est. completion date | June 2005 |
| Est. primary completion date | |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | N/A and older |
| Eligibility |
INCLUSION CRITERIA FOR HEALTHY VOLUNTEERS Age: 18 years to 100 years Normal physical and neurological examinations EXCLUSION CRITERIA FOR HEALTHY VOLUNTEERS Contraindications for transcranial magnetic stimulation: pacemaker, implanted medical pump, metal plate in skull, metal objects inside the eye or skull, history of seizures INCLUSION CRITERIA FOR STROKE PATIENTS Age: 18 years to 100 years Single ischemic or hemorrhagic hemispheric stroke at least one year before enrollment in study, confirmed by neuroimaging studies (computerized tomography or magnetic resonance imaging). Ability to perform the Jebsen-Taylor test. EXCLUSION CRITERIA FOR STROKE PATIENTS More than one stroke. Other brain lesions (i.e., traumatic brain injury, brain tumor) or neurological problems (i.e., multiple sclerosis, dementia, Parkinson's disease) Depression or poor motivational capacity Serious cognitive deficits (defined as equivalent to a mini-mental state exam score of 20 or less). Inability to understand instructions for the Jebsen-Taylor test. Uncontrolled medical problems including 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, uncontrolled epilepsy Contraindications for transcranial magnetic stimulation: pacemaker, implanted medical pump, metal plate in skull, metal objects inside the eye or skull, history of seizures |
N/A
| Country | Name | City | State |
|---|---|---|---|
| United States | National Institute of Neurological Disorders and Stroke (NINDS) | Bethesda | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| National Institute of Neurological Disorders and Stroke (NINDS) |
United States,
Boyd LA, Winstein CJ. Implicit motor-sequence learning in humans following unilateral stroke: the impact of practice and explicit knowledge. Neurosci Lett. 2001 Jan 26;298(1):65-9. — View Citation
Bridgers SL, Delaney RC. Transcranial magnetic stimulation: an assessment of cognitive and other cerebral effects. Neurology. 1989 Mar;39(3):417-9. — View Citation
Bütefisch C, Hummelsheim H, Denzler P, Mauritz KH. Repetitive training of isolated movements improves the outcome of motor rehabilitation of the centrally paretic hand. J Neurol Sci. 1995 May;130(1):59-68. — View Citation
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT06052553 -
A Study of TopSpin360 Training Device
|
N/A | |
| Completed |
NCT05511077 -
Biomarkers of Oat Product Intake: The BiOAT Marker Study
|
N/A | |
| Recruiting |
NCT04632485 -
Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
|
||
| Completed |
NCT05931237 -
Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults
|
N/A | |
| Terminated |
NCT04556032 -
Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women
|
N/A | |
| Completed |
NCT04527718 -
Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT04107441 -
AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects
|
Phase 1 | |
| Completed |
NCT04065295 -
A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225
|
Phase 1 | |
| Completed |
NCT04998695 -
Health Effects of Consuming Olive Pomace Oil
|
N/A | |
| Completed |
NCT01442831 -
Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects
|
Phase 1 | |
| Terminated |
NCT05934942 -
A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood
|
Phase 1 | |
| Recruiting |
NCT05525845 -
Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI
|
N/A | |
| Completed |
NCT05515328 -
A Study in Healthy Men to Test How BI 685509 is Processed in the Body
|
Phase 1 | |
| Completed |
NCT04967157 -
Cognitive Effects of Citicoline on Attention in Healthy Men and Women
|
N/A | |
| Completed |
NCT05030857 -
Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects
|
Phase 1 | |
| Recruiting |
NCT04494269 -
A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls
|
Phase 1 | |
| Recruiting |
NCT04714294 -
Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers
|
Phase 1 | |
| Completed |
NCT04539756 -
Writing Activities and Emotions
|
N/A | |
| Recruiting |
NCT04098510 -
Concentration of MitoQ in Human Skeletal Muscle
|
N/A | |
| Completed |
NCT03308110 -
Bioavailability and Food Effect Study of Two Formulations of PF-06650833
|
Phase 1 |