Phase
Condition
N/ATreatment
Digital Speech Application
Clinical Study ID
Ages > 30 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
PD:
Male or female age 30 years or older at Screening Visit.
Diagnosis of PD as defined by MDS PD diagnostic criteria [1]
PD severity at Screening Visit of either:
PD Hoehn and Yahr Stage 1-2, inclusive (PD Cohort I)
PD Hoehn and Yahr Stages 3-4, inclusive (PD Cohort II)
Able and willing to complete all aspects of the study, including at home smartphoneapp and Zoom telehealth assessments.
Able to provide informed consent.
Prodromal PD:
Confirmation that participant is eligible based on clinician determined predictivecriteria of known risk of PD including
Rapid eye movement sleep behavior disorder (RBD), possible, probable ordefinite, OR
Hyposmia defined as less than 10th percentile on University of PennsylvaniaSmell Identification Test (UPSIT), age and gender adjusted, OR
Known genetic variants associated with PD risk, AND Confirmed eligible DATscan.
Male or female age 30 or older at Screening Visit.
Able and willing to complete all aspects of the study, including at home smartphoneapp and Zoom telehealth assessments
Able to provide informed consent.
Age & Sex Matched Healthy Control:
Male or female age 30 years or older at Screening visit.
Able and willing to complete all aspects of the study, including at home smartphoneapp and Zoom telehealth assessments
Able to provide informed consent.
Exclusion
Exclusion Criteria:
PD:
Late-stage PD diagnosis (i.e., Hoehn & Yahr Stage 5) at Screening Visit
Symptomatic or atypical PD syndromes due to either drugs (e.g., metoclopramide,flunarizine, neuroleptics) or metabolic disorders (e.g., Wilson's disease),encephalitis, or degenerative diseases (e.g., progressive supranuclear palsy).
Current or active clinically significant neurological disorder other than PD (in theopinion of the Investigator).
Significant cognitive impairment or clinical dementia at Screening that, in theopinion of the Investigator, would interfere with study evaluation.
History of drug and/or alcohol abuse within the past year prior to Screening Visit.
Inability or unwillingness to complete all aspects of the study - including use of aprovisioned smartphone for study assessments; completion of telehealth assessments.
Any other medical or psychiatric condition, which in the opinion of the investigatormight preclude participation.
Prodromal PD:
Clinical diagnosis of PD, other parkinsonism, or dementia.
Any current or active clinically significant neurological disorder (in the opinionof the Investigator).
Previously obtained MRI scan with evidence of clinically significant neurologicaldisorder (in the opinion of the Investigator).
Significant cognitive impairment or clinical dementia at Screening that, in theopinion of the Investigator, would interfere with study evaluation.
History of drug and/or alcohol abuse within the past year prior to Screening Visit.
Inability or unwillingness to complete all aspects of the study - including use of aprovisioned smartphone for study assessments; completion of telehealth assessments.
Any other medical or psychiatric condition, which in the opinion of the investigatormight preclude participation.
Age & Sex Matched Healthy Control:
First degree relative with PD (i.e., biologic parent, sibling, child).
Any current or active clinically significant neurological disorder (in the opinionof the Investigator).
Previously obtained MRI scan with evidence of clinically significant neurologicaldisorder (in the opinion of the Investigator).
Significant cognitive impairment or clinical dementia at Screening that, in theopinion of the Investigator, would interfere with study evaluation.
History of drug and/or alcohol abuse within the past year prior to Screening Visit.
Inability or unwillingness to complete all aspects of the study - including use of aprovisioned smartphone for study assessments; completion of telehealth assessments.
Any other medical or psychiatric condition, which in the opinion of the investigatormight preclude participation
Study Design
Study Description
Connect with a study center
Northwestern University
Chicago, Illinois 60611
United StatesActive - Recruiting
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