Enhancing Upper Limb Prostheses With Radio Frequency Identification

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-08-31

Study Completion Date

2014-06-30

Brief Summary

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The purpose of this study is to determine if Radio Frequency Identification (RFID) can lead to greater prosthesis function and control. Subjects are asked to perform specific tasks and actions using the traditional control method, as well as RFID control.

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Detailed Description

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Conditions

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Below Elbow Amputation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Functional Assessment

Participant will be asked to perform a series of tasks involving their prosthesis. These tasks can involve switching grips as well as moving objects.

Group Type EXPERIMENTAL

Morph

Intervention Type DEVICE

Morph is a small electric controller that is retrofit into existing myoelectric prostheses to equip them with wireless identification capabilities. Specifically, Morph allows the prosthesis to react to RFID tags in the environment.

Interventions

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Morph

Morph is a small electric controller that is retrofit into existing myoelectric prostheses to equip them with wireless identification capabilities. Specifically, Morph allows the prosthesis to react to RFID tags in the environment.

Intervention Type DEVICE

Other Intervention Names

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Myoelectrically-Operated RFID Prosthetic Hand

Eligibility Criteria

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Inclusion Criteria

1. Age 18 or greater.
2. Below elbow amputation, unilateral or bilateral.
3. Chronic stable amputation: \> 6 months from amputation.
4. Stable prosthesis prescription: \> 3 months since last major prosthesis modification.
5. Cognitively intact, as determined by Mini-Mental Status Examination score \> 24.
6. Able to provide informed consent and available to participate in study activities.
7. No severe residual limb motor/sensory impairment or pain likely to interfere with treatment.
8. Expected to be medically and psychiatrically stable for study duration.