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OpenTrials
Completed

NCT Number: NCT02125825

Ambulatory Parkinson's Disease Dyskinesia Monitor for Drug Therapy Titration

The objective is to assess a compact, portable, wireless movement disorder system with continuous monitoring capabilities to detect and quantify the severity of levodopa-induced dyskinesia in Parkinson's disease.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Johns Hopkins Medical Center, Baltimore, Maryland, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of idiopathic Parkinson's disease
  • Clinical history of levodopa-induced dyskinesia
  • 21 Years of age or older
  • Stage 2 - 4 OFF-medication on the Hoehn and Yahr scale

Exclusion criteria

  • Dementia (determined by a neuropsychological assessment)
  • Severe tremor unaffected by levodopa

Treatment and study plan

Primary outcomes

  1. Correlation between motion sensor features and clinician-rated dyskinesia severity

    Time frame: All data will be collected within a single session not to exceed 3 hours

    Motor function (movement speed and magnitude measured with a motion sensor) will be collected for a period of 2 hours after taking normally prescribed dose of levodopa.

Sponsors and collaborators

Lead sponsor

Great Lakes NeuroTechnologies Inc.

Industry

Collaborators

  • Johns Hopkins University
  • National Institute on Aging (NIA)
  • University of Rochester

Registry information

Official study title

Kinesia-D Phase II In-Clinic Continuous Assessment Study

Acronym: Kinesia-D

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Apr 29, 2014
Registry last updated
Jan 12, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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