Study Stopped
Lack of study participants, no data published.
WiiMote Game Controller as a Device to Study Movement Disorders
1 other identifier
observational
250
1 country
1
Brief Summary
Purpose of the study: The purpose of this study is to investigate the Wii remote game control device for use in the study of Movement Disorders. The term "Movement Disorders" refers to a group of abnormal medical conditions characterized by involuntary body movements. Current treatment of these disorders is primarily geared to improve symptoms. Rating scales are usually used to grade response to treatment. These rating scales require special training, take a lot of time, and often present with great variability. Thus, the development of a simple device to perform efficacy measurements offers a great advantage over current methods and is less costly.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2007
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2007
CompletedFirst Submitted
Initial submission to the registry
December 2, 2008
CompletedFirst Posted
Study publicly available on registry
December 4, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2014
CompletedSeptember 1, 2014
August 1, 2014
5.8 years
December 2, 2008
August 29, 2014
Conditions
Study Arms (2)
Control Group
Participants with no movement disorders.
Movement Disorders Participants
Participants have a movement disorder
Eligibility Criteria
18 Years and older, females of childbearing potential, healthy volunteers and adults with movement disorders.
You may qualify if:
- Men and women, aged 18 or older, with abnormal movements (including tremor, chorea, dystonia, myoclonus, and tic) and normal controls (subjects without abnormal movements).
- Subjects must be willing and able to comply with study procedures.
- Patients must be willing and able to give meaningful, written informed consent.
You may not qualify if:
- \. Significant cognitive impairment which, in the opinion of the Investigator, would interfere with the ability to complete all the tests required in the protocol.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Vanderbilt Universitylead
- National Parkinson Foundationcollaborator
- Robertson County Parkinson Support Groupcollaborator
Study Sites (1)
Vanderbilt University Medical Center
Nashville, Tennessee, 37232-2551, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Thomas L Davis, MD
Department of Neurology/Movement Disorders
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
December 2, 2008
First Posted
December 4, 2008
Study Start
August 1, 2007
Primary Completion
May 1, 2013
Study Completion
August 1, 2014
Last Updated
September 1, 2014
Record last verified: 2014-08