Objective, Passive Assessment of LRRK2 Carriers (OPAL)

  • STATUS
    Recruiting
  • End date
    Jul 31, 2023
  • participants needed
    10
  • sponsor
    University of Rochester
Updated on 12 May 2022
movement disorder
Online studies

Summary

This study is currently only open to active participants in the University of Rochester’s VALOR-PD study. The goal of this project is to identify objective, sensitive, and convenient measures for assessing early signs of Parkinson's disease in an at-risk population at home. We will do so by using a wireless sensor and analyzing the radio signals that bounce off patients' bodies, while patients go about their normal life without needing to wear sensors, answer questionnaires, or actively perform any tests.

Description


Details
Condition Parkinson Disease
Treatment Emerald device
Clinical Study IdentifierNCT05287620
SponsorUniversity of Rochester
Last Modified on12 May 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

At least 50 years of age
Able and willing to provide informed consent
English fluency
U.S. resident
LRRK2 G2019S gene carrier, determined by participation in VALOR-PD
Mild parkinsonian signs, determined by modified Movement Disorder Society-Unifeid Parkinson's Disease Rating Scale (MDS-UPDRS) score from the most recent VALOR-PD visit
Have WiFi in their residence
Access to a smartphone or tablet

Exclusion Criteria

Inability to complete study activities, as determined by the study team
Any medical or psychiatric condition that, in the study team's judgement, would preclude participation
Self-reported or VALOR-PD investigator determined Parkinson's disease
Any movement disorder (e.g. essential tremor)
Currently taking neuroleptics or other drugs known to cause parkinsonism
Pregnancy
Non-ambulatory status
More than one ambulatory pet in the household
More than two individuals in the household (not including participant)
these criteria can be waived at the discretion of the investigators
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What happens next?
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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