A Study to Gather Data for Maintaining Mobility and Quality of Life for Manual Wheelchair Users

Overview

Información sobre este estudio

The purpose of this study is to develop a pattern recognition algorithm for manual wheelchair related activities of daily living. This study also aims to identify shoulder impingement risk score of MWC-related ADLs and determine cumulative shoulder impingement risk of MWC-related ADLs.

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.

Group 1: Adults with an SCI who use a manual wheelchair

Group 2: Able-bodied adults

Inclusion Criteria:

  • Group1
    • Age 18-70 at time of enrollment
    • Traumatic or non-traumatic SCI
    • Uses a manual wheelchair as primary mode of mobility for >1 year
    • Independently mobile enough to participate in the study
    • Willingness to participate in the study
    • Active shoulder range of motion within limits needed for the tasks performed during the study
  • Group 2
    • 18-70 years of age
    • Able to walk independently with no reliance on an orthotic, prosthetic, or gait aid
    • Functional upper extremity range of motion
    • Willingness to participate in study

Exclusion Criteria: 

  • Group 1
    • Surgery or significant injury to the shoulder(s) of interest (such as dislocation, fracture or full rotator cuff tear) in which return to pre-injury functional status was NOT attained
    • Peripheral nerve impairment of the upper extremity being tested
    • Evidence of significant denervation of multiple scapular muscles
    • Shoulder or wrist instability on the upper extremity to be tested
    • Allergy to medical grade adhesive tape (used to secure sensors to skin)
  • Group 2
    • Any documented musculoskeletal or neurological disorders that would be expected to impact shoulder health or change ability to walk independently
    • Previous diagnosis of shoulder tears prior to enrollment or suspected tendon tears with physical exam

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

Rochester, Minn.

Investigador principal de Mayo Clinic

Melissa Morrow, Ph.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
.
CLS-20307352

Mayo Clinic Footer