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Kinesia 360 Parkinson's Monitoring Study | Clinical Trials | Clareo Health

COMPLETEDNA

Kinesia 360 Parkinson's Monitoring Study

Kinesia 360 Multi-Center Parkinson's Monitoring Study

NCT02657655•Great Lakes NeuroTechnologies Inc.

Summary

Kinesia 360 is an ambulatory symptom monitoring device for Parkinson's Disease (PD). The aim of this study is to investigate the impact, validation, and usability of the Kinesia 360 system.

Detailed Description

This is a five-month study of 45 subjects (approximately 15 subjects per site), consisting of adult volunteers that have been clinically diagnosed with Parkinson's disease. Subjects will have a confirmed history of motor fluctuation with a variety of Parkinson's disease symptom severities. All subjects will user the Kinesia 360 system and complete motor diaries several times per month during the study period. Symptom reports will be provided to the treating clinical team. Motor function, quality of life, engagement, and satisfaction with care will be tracked throughout the study.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Idiopathic Parkinson's Disease,
•History of motor fluctuations (2 hrs/day of Off time and/or 1 hr/day of troublesome dyskinesia)
•Fluent in English

Exclusion Criteria

•Inability to carry out study activities
•Subjects with cognitive deficits that would prevent following instructions and serious medical conditions that would compromise a subject's safety
•Subjects who have dementia, exhibited by Montreal Cognitive Assessment (MoCa) score of 22 or less.
•Subjects who have had Deep Brain Stimulation (DBS) surgery less than 6 months prior to study enrollment, or who are deemed by the study investigator to be highly likely to undergo DBS surgery during the 6 month study period.

Locations (4)

Johns Hopkins University

Baltimore, Maryland, United States

University of Rochester

Rochester, New York, United States

Cleveland Clinic

Cleveland, Ohio, United States

Greenville Health System

Greenville, South Carolina, United States

Key Dates

Start Date

January 1, 2016

Primary Completion Date

February 1, 2017

Completion Date

February 1, 2017

Last Updated

February 19, 2018

Enrollment

ESTIMATED participants

Conditions

Parkinson's Disease

Interventions

Kinesia 360

DEVICE

Deep Brain Stimulation Therapy in Movement Disorders

NCT02119611

Parkinson's Disease

View study

RECRUITINGPHASE1

Research Into the Safety of a New Agent (VT-5006) in People With and Without Parkinson's Disease

NCT07310264

Healthy Volunteers (HV)Parkinson's Disease (PD)

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RECRUITINGNA

Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-PD) China Study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: February 19, 2018Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Kinesia 360 Parkinson's Monitoring Study

Inclusion Criteria

Exclusion Criteria

Deep Brain Stimulation Therapy in Movement Disorders

Research Into the Safety of a New Agent (VT-5006) in People With and Without Parkinson's Disease

Adaptive DBS Algorithm for Personalized Therapy in Parkinson's Disease (ADAPT-PD) China Study

A Study to Evaluate the Efficacy and Safety of Intravenous (IV) Prasinezumab in Participants With Early-Stage Parkinson's Disease

Effect of Striatal Temporal Interference Stimulation on Language Processing in Neurodegenerative Diseases

SAD Study in Patients With Parkinson's Disease and Motor Fluctuations