NCT00802191

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
250

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2007

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
terminated

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

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

December 2, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 4, 2008

Completed
4.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2013

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2014

Completed
Last Updated

September 1, 2014

Status Verified

August 1, 2014

Enrollment Period

5.8 years

First QC Date

December 2, 2008

Last Update Submit

August 29, 2014

Conditions

Study Arms (2)

Control Group

Participants with no movement disorders.

Movement Disorders Participants

Participants have a movement disorder

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Vanderbilt University Medical Center

Nashville, Tennessee, 37232-2551, United States

Location

MeSH Terms

Conditions

Parkinson DiseaseEssential Tremor

Condition Hierarchy (Ancestors)

Parkinsonian DisordersBasal Ganglia DiseasesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMovement DisordersSynucleinopathiesNeurodegenerative Diseases

Study Officials

  • Thomas L Davis, MD

    Department of Neurology/Movement Disorders

    PRINCIPAL INVESTIGATOR

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

Locations