Clinical Trials Logo

Clinical Trial Summary

This is a study being performed to evaluate the safety and effectiveness of 3D printed myoelectric prosthetic devices in children with a congenital upper limb deficiency.


Clinical Trial Description

The purpose of this study is to learn more about whether myoelectric prosthetic devices would be beneficial and useful for children. The study protocol specifies 4 study visits over the course of a year at the following intervals: baseline, 3 month, 6 month, 12 months. In following the protocol, each study visit will use the Assessment of Capacity for Myoelectric Control (ACMC) functional testing. The study participants will also complete several parent-child reported health related quality of life and musculoskeletal questionnaires. Specifically, the Pediatric Outcomes Data Collection Instrument (PODCI), the Pediatric Quality of Life Inventory (PedsQL), and the Children's Hand-Use Experience Questionnaire (CHEQ) will be used to measure efficacy of the myoelectric devices.. ;


Study Design


Related Conditions & MeSH terms

  • Upper Extremity Deformities, Congenital
  • Upper Limb Deformities, Congenital

NCT number NCT04059107
Study type Interventional
Source Oregon Health and Science University
Contact
Status Enrolling by invitation
Phase N/A
Start date July 3, 2019
Completion date December 31, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT04199975 - Customized Self-Controlled Power-Driven or Mechanical Orthoses for the Upper Limb - A Pilot Study N/A