A Study to Evaluate SoftHand Pro for Daily Activities of Transradial Amputees

Overview

Información sobre este estudio

The purpose of this study is to compare the performance of the SoftHand Pro (SHP) and Ossur i-Limb in grasping and manipulations tasks, and to determine how grasping and manipulation performance improves over time with each device.  Data will also be obtained regarding usage patterns and user satisfaction with each device.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • the individual can successfully use their prosthesis, list the components used and that their current prosthesis is fitting properly (by performing a tension analysis);
  • the individual had a unilateral transradial amputation more than 6 months before the clinical evaluation because, to use a myoelectric prosthesis, the residual limb volume needs to be stable;
  • the individual is a current user of one of two common myoelectric prosthetic hands: Sensor Hand Speed and Bebionic (both Ottobock).

Exclusion Criteria: 

  • individuals who have had transradial amputation for less than 6 months;
  • individuals who have been fit and trained to use a prosthesis but chose not to use one;
  • clinical history of brachial plexopathy, cervical radiculopathy or polyneuropathy;
  • orthopedic, joint degeneration (i.e., arthritis, self-reported) affecting the hand or cervical spine that severely limit upper limb function (observed);
  • visual problems that would interfere with the grasping;
  • co-existing central nervous system disease with symptoms that limit upper extremity function (e.g., multiple sclerosis, motor neuron disease, myasthenia gravis, Parkinson’s disease, dystonia) revealed in medical history;
  • limited range of motion as assessed through range of motion testing;
  • inability to follow study instructions;
  • use of medications that might affect sensory and/or motor functions.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Kristin Zhao, Ph.D., M.S.

Abierto para la inscripción

Contact information:

Tyson Scrabeck CCRP

(507) 538-1016

Scrabeck.Tyson@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20551328

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