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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00473161
Other study ID # EMG biofeedback
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received May 11, 2007
Last updated May 21, 2014
Start date May 2007

Study information

Verified date May 2014
Source University of Southern California
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

A newly-developed device for biofeedback of surface EMG will be used to either increase or decrease activity in the muscles of children with poor reaching due to cerebral palsy.


Description:

Children ages newborn to 21 with a diagnosis of arm weakness, hypertonia, or hyperkinesia due to cerebral palsy will be recruited. A muscle that is either over-active or under-active will be selected for each child. The child will be provided with the device to wear for 1 month in order to call attention to the identified muscle. At the beginning and end of the month, reaching will be assessed using three-dimensional kinematic motion capture. The outcome measure will be the speed and curvature of reaching to a target in front of the child.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 1 Month to 21 Years
Eligibility Inclusion Criteria:

- weakness, hypertonia, or hyperkinetic disorder affecting one or both arms

- reduced speed or quality of reaching

Exclusion Criteria:

- any condition that would increase the risk of participation

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
surface EMG biofeedback


Locations

Country Name City State
United States Stanford University Stanford California

Sponsors (1)

Lead Sponsor Collaborator
University of Southern California

Country where clinical trial is conducted

United States, 

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