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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Key Participation Requirements

Gender

Female, Male

Age Range

30 Years and older

Trial Duration

06/01/2009 - 12/01/2009

Study Type

Observational