Bradykinesia Subscale Administered Alone Versus Regular Administration

Study Title
Bradykinesia Subscale Administered Alone Versus Regular Administration: Psychometric Properties
Teva Identifier
PM105
ClinicalTrials.gov Identifier
NCT00932581
Study Status
Completed
Trial Condition(s)
Parkinson's Disease
Interventions
Other: Bradykinesia UPDRS Motor Full Examination | Other: Bradykinesia subscale of UPDRS Motor Examination

Study Description

Please refer to ClinicalTrials.gov for a description of the trial
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Participation criteria and map of study locations


Key Participation Requirements

Gender
Female, Male
Age group
Adult, Older Adult
Age Range
30 Years and older
Trial Duration
06/01/2009 - 12/01/2009

Study Type

Observational