Development of a Simulation Tool for Upper Extremity Prostheses

NCT ID: NCT01622530

Last Updated: 2018-09-18

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2010-07-31
• Study Completion Date: 2017-12-31

Brief Summary

Amputees often choose not to wear prostheses due to marginal performance or may settle for a prosthesis that offers only cosmetic improvement, but lacks function. A simulation tool consisting of a robotics-based human body model (RHBM) to predict functional motions, and integrated modules for aid in prescription, training, comparative study, and determination of design parameters of upper extremity prostheses will be developed.

The main objective of collecting and analyzing human movement during several common tasks is to optimize and validate the robotics based human model. The range of motion data of subjects performing activities of daily living such as opening a door, turning a wheel, grooming, eating, bilateral lifting, as well as recreational and sport activities such as swinging a baseball bat, and golf club will be analyzed. This motion analysis data will also be used to compare data between four groups: a control group (n=10), a braced group simulating prosthesis use (n=10), a group wearing a transradial prosthesis (n=10) and a group wearing a transhumeral prosthesis (n =10).

Detailed Description

Data will be collected by an 8 camera Vicon© motion analysis system during one 3-4 hour testing period. Forty-five reflective markers will be attached to subjects skin and clothing via a double sided adhesive electrode collar. The cameras work on an infrared spectrum and the markers are passive reflective spheres. Relations between marker positions and anatomical / known positions on the body are used to calculate the positions of body segments.This analysis will provide information on movement strategies, compensatory motion, and socket movement associated with the selected tasks for transradial and transhumeral prostheses. Differences in the range of motion of the prostheses users and control subjects will be calculated to determine compensatory motion. The movement of the prosthesis's socket as a function of task and other factors will also be measured. Measured data will be used to minimize error in the simulation of the upper body movement. Knowledge of human motor function given in the recorded data can be extended to give insight to movement parameters when designing new prosthetics. Simulations will be optimized to the collected data using a regressive best fit method.

Conditions

Traumatic Amputation of Upper Limb, Level Unspecified

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Amputees

upper limb amputees

No interventions assigned to this group

Non-amputees

No longer recruiting non-amputees

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• All subjects will be capable of providing an informed consent.
• Normal healthy adult subjects and upper limb amputees that currently use a prosthesis to complete activities of daily living will be included.

Exclusion Criteria

• Subjects younger than 18 or older than 65 will be excluded.
• Adults that are unable to consent will be excluded from the study.
• Subjects that have health issues or injuries that would prevent them from lifting five pounds or completing simple tasks of daily living will be excluded from the study.
• Subjects will be asked if they are able to lift five pounds, open a door and drink from a cup without pain or injury. Before study set up and recording begins, subjects will be asked to practice these tasks to insure that they are capable of completing them.
• Pregnant women will be excluded from this study due to the changes in some physical abilities during pregnancy.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of South Florida

OTHER

Sponsor Role: lead

Responsible Party

Stephanie L. Carey

Assistant Research Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Rajiv Dubey, PhD

Role: PRINCIPAL_INVESTIGATOR

University of South Florida

Locations

University of South Floria RRT building

Tampa, Florida, United States

Countries

United States

Related Links

http://carrt.eng.usf.edu

Center for Rehabilitation, Robotics and Assistive Technologies

Other Identifiers

09128006

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

Pro00000991

Identifier Type: -

Identifier Source: org_study_id