Human Movement Database

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-99
SponsorNational Institutes of Health Clinical Center (CC)

About this trial

This study will collect information on the different ways people control limb and body movements. This information will be used to develop a database on normal movements and adaptive movements of people who have diseases that affect the way they move. The database will serve as a tool to improve diagnosis and treatment of patients with movement-related problems.

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Children; One month old to 17 years of age

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

Disqualifiers

Individuals with pacemakers

Pregnancy

Adults unable to provide informed consent

Trial population

Normal/healthy volunteers and volunteers with impairments of the neuromusculoskeletal system. Subjects will be evenly distributed between males and females

Trial design

Design model

Case-control

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

7,500 Participants
are grouped into 2 trial groups
Group A: healthy volunteer
Group B: Impaired volunteer

Trial outcomes

Primary outcomes

1

Gait Kinematics

Strength and spasticity testing both include torque or force measurements as the primary outcomes. Balance testing typically yields the amount, velocity and direction of sway in response to different conditions or perturbations.

Time frame
end of testing

Secondary outcomes

Other outcomes

Sponsors and contacts

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