This study is currently recruiting participants.
Number
90-CC-0168
Sponsoring Institute
National Institutes of Health Clinical Center (CC)
Recruitment Detail
Type: Participants currently recruited/enrolled Gender: Male & Female Min Age: 1 Mo Max Age: 99 Years
Referral Letter Required
No
Population Exclusion(s)
Pregnant Women
Keywords
Biomechanics; Kinesiology; Walking; Natural History
Recruitment Keyword(s)
None
Condition(s)
Movement Disorder
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Supporting Site
NIH Clinical Center
Volunteers from one month old to old age who have normal movement patterns or who have developed different ways to perform movement tasks may be eligible for this study. A physician or physical therapist will screen candidates to determine their strength, flexibility and range of motion of joints.
Participants will be asked to perform movements such as walking, walking up or down stairs, standing quietly or reaching for an object or using treadmill. For the test, the arms and legs are wrapped with a soft, rubber-like material to which small plastic reflective balls are attached. A piece of firm material called a shell may be attached to the rubber sleeves or other areas of the body. Then the volunteer performs the specified task several times while special cameras record the movement. These cameras will record the positions of the reflective balls during movement and may show the person s face or body. Electrical activity in the muscles also may be measured, using small metal electrodes attached to the surface of the skin with an adhesive bandage.
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INCLUSION CRITERIA: Individuals with neuromuscular disorders and Healthy Volunteers in order to be eligible to participate in this study, must meet all of the following criteria: -Children; One month old to 17 years of age --In the case of infants and very young children, they need to be able to imitate or perform an action on cue (e.g., reach out for a toy that is presented or take steps if placed on a treadmill) based on the parent report if the subject is a child and physician observation during history and physical examination. -Adults; 18 years 99 years -In good general health as evidenced by medical history or diagnosed with impairment of neuromusculoskeletal system -Stated willingness to comply with all study procedures and availability for the duration of the study -Provision of signed and dated informed consent form -For those participants older than 5 years of age who have an abnormal gait pattern when walking as a result of a central nervous system injury, Dr. Alter will ask them or their guardian about their seizure history EXCLUSION CRITERIA: Individuals with neuromuscular disorders and Healthy Volunteers, who meets any of the following criteria will be excluded from participation in this study: -Individuals with pacemakers -Pregnancy -Adults unable to provide informed consent
Individuals with neuromuscular disorders and Healthy Volunteers in order to be eligible to participate in this study, must meet all of the following criteria:
-Children; One month old to 17 years of age
--In the case of infants and very young children, they need to be able to imitate or perform an action on cue (e.g., reach out for a toy that is presented or take steps if placed on a treadmill) based on the parent report if the subject is a child and physician observation during history and physical examination.
-Adults; 18 years 99 years
-In good general health as evidenced by medical history or diagnosed with impairment of neuromusculoskeletal system
-Stated willingness to comply with all study procedures and availability for the duration of the study
-Provision of signed and dated informed consent form
-For those participants older than 5 years of age who have an abnormal gait pattern when walking as a result of a central nervous system injury, Dr. Alter will ask them or their guardian about their seizure history
EXCLUSION CRITERIA:
Individuals with neuromuscular disorders and Healthy Volunteers, who meets any of the following criteria will be excluded from participation in this study:
-Individuals with pacemakers
-Pregnancy
-Adults unable to provide informed consent
Principal Investigator
Referral Contact
For more information: