- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02368223
Feasibility of the Portable YouGrabber System (YouGrabber)
July 23, 2015 updated by: University Children's Hospital, Zurich
Feasibility of a Home-based Interactive System for Upper Limb Therapy (YouGrabber)
The aim of the study is to determine the feasibility of the portable version of the YouGrabber® system in children with central motor disorders.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Interventional
Enrollment (Actual)
15
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Affoltern am Albis, Switzerland, CH-8910
- University Children's Hospital Zurich, Rehabilitation Centre Affoltern am Albis
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
5 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: YouGrabber training
Home-based YouGrabber training
|
2 weeks of home-based therapy with a virtual-reality enhanced upper limb training system
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
User satisfaction (Questionnaire about usability, motivation, general opinion)
Time Frame: week 2
|
Questionnaire about usability, motivation, general opinion
|
week 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Device usage (Total time of exercise per week; time of training session)
Time Frame: week 2
|
Total time of exercise per week; time of training session
|
week 2
|
Error rate (Error prone games; application problems as a home-based system)
Time Frame: week 2
|
Error prone games; application problems as a home-based system
|
week 2
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Corinna Gerber, MSc, University Children's Hospital Zurich, Rehabilitation Centre Affoltern am Albis
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2014
Primary Completion (Actual)
July 1, 2015
Study Completion (Actual)
July 1, 2015
Study Registration Dates
First Submitted
February 13, 2015
First Submitted That Met QC Criteria
February 20, 2015
First Posted (Estimate)
February 23, 2015
Study Record Updates
Last Update Posted (Estimate)
July 24, 2015
Last Update Submitted That Met QC Criteria
July 23, 2015
Last Verified
July 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Brain Diseases
- Wounds and Injuries
- Congenital Abnormalities
- Brain Damage, Chronic
- Craniocerebral Trauma
- Trauma, Nervous System
- Nervous System Malformations
- Neural Tube Defects
- Spinal Dysraphism
- Cerebral Palsy
- Brain Injuries
- Brain Injuries, Traumatic
- Nervous System Diseases
- Meningomyelocele
- Spina Bifida Cystica
- Central Nervous System Diseases
Other Study ID Numbers
- YouGrabber_Feasibility_2014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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