SBIR/STTR Research Award

Kinematic Biofeedback for Independent Motor Retraining

Award identifier 6743a06d4d1d381cfebeb64cfeb5b6e9be45d03ad5bf2346c9d3ff58c0bb6152Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$217,501

Program and phase

SBIR · Phase I

Award year

2005

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CUSTOMKYNETICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2005-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): This project proposes to develop a device that will improve the quality and availability of motor retraining for individuals with neuromotor disorders due to stroke or incomplete spinal cord injury. Biofeedback of postural control variables such as ground reaction force and center of pressure sway has been used effectively, however, existing devices are not suitable for use by many patients and are not widely available. We propose to develop a therapeutic system that enables patients to practice clinically-relevant, closed chain, lower-extremity tasks (sit-to-stand transitions and balance shifts) and that uses visual biofeedback of kinematic variables to encourage use of the affected limb(s). We anticipate that use of the proposed device will improve the efficacy of traditional therapy by allowing patients to begin sit-to-stand and balance shift exercises earlier in the rehabilitation process because the proposed mechanical device will reduce the risk of falls. In Phase I we will: 1} modify an existing exercise device to provide visual biofeedback of measured variables, 2) develop clinically relevant biofeedback exercises, 3) evaluate the biofeedback displays in a study involving age-matched individuals without a neuromotor deficit, and 4) demonstrate feasibility of the approach in a pilot study where patients use the device as one component of their traditional therapy during acute rehabilitation following stroke. The pilot study wilt provide insight into the following objectives: 1) determine if the device can be used safely for this population, 2} determine if patients can understand the biofeedback information and complete the specified tasks, 3) determine if the device is viewed as a beneficial form of therapeutic exercise by both physical therapists and patients, and 4) determine if a rehabilitation program using the device improves the rate of recovery and/or the efficacy of traditional therapy. In Phase II we will improve the biofeedback interface, optimize the protocols to improve transference, develop custom electronics to generate the biofeedback displays, and test the system in an extensive clinical trial. The target market for the device is rehabilitation hospitals and clinics that serve patients following stroke or incomplete spinal cord injury.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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