NCT00932581
Completed
Not Applicable
Investigation of the Psychometric Properties of the Bradykinesia Subscale When Administered Alone Versus as a Component of the Entire Motor Examination Section of the Unified Parkinson's Disease Rating Scale
ConditionsParkinson's Disease
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Parkinson's Disease
- Sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
- Enrollment
- 110
- Primary Endpoint
- Scores on the UPDRS motor evaluation subscale are equivalent.
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
The purpose of this study is to examine whether scores on questionnaires that rate how much Parkinson's Disease (PD) has slowed movements of the body differ when the order of the questions are changed. The consistency and accuracy of the questionnaires will also be examined. It is hypothesized that there will not be a difference.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Male or Female at least 30 years of age
- •Willing to be assessed using the motor examination section of the UPDRS and the SPES/SCOPA motor evaluation
- •Patients must be willing and able to give written informed consent prior to performing an study procedures
- •Be in the "ON" State (only for patients who fluctuate between "ON" and "OFF" states)
Exclusion Criteria
- •Absence of bradykinesia at the time of assessment
- •Hoehn and Yahr stage not available from patient's chart or not assessed between 3 and 180 days prior to clinic visit
- •Has received and experimental drug within the last thirty (30) days
Outcomes
Primary Outcomes
Scores on the UPDRS motor evaluation subscale are equivalent.
Time Frame: 4 months
Secondary Outcomes
- Correlations between the UPDRS motor examination bradykinesis subscale and the remaining UPDRS motor examination items, Hoeh and Yahr stage, Schwab and England scale, and SPES/SCOPA motor evaluation.(4 months)
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