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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02368223
Other study ID # YouGrabber_Feasibility_2014
Secondary ID
Status Completed
Phase N/A
First received February 13, 2015
Last updated July 23, 2015
Start date October 2014
Est. completion date July 2015

Study information

Verified date July 2015
Source University Children's Hospital, Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Interventional

Clinical Trial 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.


Description:

In a feasibility trial with the portable version of the YouGrabber® system it will be determined if the technique and equipment are ready to be used in a home setting where children with central motor disorders train with assistance of caregivers but without a therapist. Furthermore, it will be examined if children and adolescents with central motor disorders accept this home-based system and if they are motivated for using it.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Both
Age group 5 Years to 18 Years
Eligibility Inclusion Criteria:

- Central motor disorders

- Ability to sit in an upright position for 45 minutes

Exclusion Criteria:

- Manual Ability Classification Scale (MACS) V

- Severe visual or auditory impairments

- Severe photosensitive epilepsy

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

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

Locations

Country Name City State
Switzerland University Children's Hospital Zurich, Rehabilitation Centre Affoltern am Albis Affoltern am Albis

Sponsors (1)

Lead Sponsor Collaborator
University Children's Hospital, Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary User satisfaction (Questionnaire about usability, motivation, general opinion) Questionnaire about usability, motivation, general opinion week 2 No
Secondary Device usage (Total time of exercise per week; time of training session) Total time of exercise per week; time of training session week 2 No
Secondary Error rate (Error prone games; application problems as a home-based system) Error prone games; application problems as a home-based system week 2 No
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