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Prospective Evaluation of Forceplate Measured Levodopa-Induced Dyskinesia

Completed
Conditions
Parkinson's Disease
Registration Number
NCT00912977
Lead Sponsor
Oregon Health and Science University
Brief Summary

Nearly all Parkinson's disease (PD) patients eventually develop abnormal and unwanted movements (dyskinesias; LID) caused by the gold standard treatment, Levodopa. The severity of these movements can range from subtle to extremely debilitating and may or may not interfere with normal activities such as putting on a coat or brushing ones teeth. The purpose of this study is to demonstrate the validity and reliability of objectively measuring dyskinesia with a forceplate.

Detailed Description

The main outcome measure of this study are measurements taken every half hour during an inpatient study visit. These measurements include standing on a forceplate for 1 minute while performing a mental task such as reciting the alphabet backwards. During this forceplate stance, a rater will visually score your movements. All participants must be eligible for another Parkinson's disease study at Oregon Health and Science University.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Parkinsons disease
  • Older than 18
Exclusion Criteria
  • Must be participating in a Parkinsons disease study at Oregon Health & Science University

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Forceplate MeasureEvery 1/2 hour
Secondary Outcome Measures
NameTimeMethod
Visual Rating Scaleevery 1/2 hour

Trial Locations

Locations (1)

Oregon Health & Science University

🇺🇸

Portland, Oregon, United States

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