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Feasibility of the Portable YouGrabber System

NCT02368223 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2015-07-24

No results posted yet for this study

Summary

The aim of the study is to determine the feasibility of the portable version of the YouGrabber® system in children with central motor disorders.

Conditions

Interventions

DEVICE

YouGrabber

2 weeks of home-based therapy with a virtual-reality enhanced upper limb training system

Sponsors & Collaborators

  • University Children's Hospital, Zurich

    lead OTHER

Principal Investigators

  • Corinna Gerber, MSc · University Children's Hospital Zurich, Rehabilitation Centre Affoltern am Albis

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
5 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2015-07-31
Completion
2015-07-31

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02368223 on ClinicalTrials.gov