Skip to content

Assessing Tele-Health Outcomes in Multiyear Extensions of PD Trials

Tele-health Outcomes as Digital Biomarkers of Parkinson's Disease Progression During Extended Follow up of STEADY-PD3 and SURE-PD3 Trial Participants

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03538262
Acronym
AT-HOME PD
Enrollment
226
Registered
2018-05-29
Start date
2018-10-01
Completion date
2022-03-21
Last updated
2023-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Keywords

SURE-PD3, STEADY-PD III, Parkinson disease, PD, Parkinson Study Group (PSG), Telemedicine, Smartphone, Disease progression, Televisits, Patient-reported outcomes

Brief summary

An observational study to characterize and compare long-term clinical outcomes data collected remotely through periodic tele-visits, interactive smartphone app sessions, and web-based surveys in individuals with Parkinson's Disease (PD) who have completed the interventional phases of the STEADY-PD3 and SURE-PD3 clinical trials.

Detailed description

Telemedicine and smartphone-based remote sensor assessments represent particularly promising opportunities to streamline study conduct, reduce participant burden, and allow for the collection of data beyond the usual episodic, in-clinic assessments. Demonstrating the utility of these relatively inexpensive accessible platforms for the measurement of PD progression would also establish the infrastructure for long-term follow up of participants after completion of interventional studies. STEADY-PD3 (a.k.a. STEADY-PD III) and SURE-PD3 were both designed as phase 3 trials of potential disease-modifying interventions in PD. In both studies, de novo PD participants were randomized in 1:1 allocation to active therapy versus placebo with longitudinal follow up for three and two years, respectively. Both studies include collection of DNA and plasma samples, which along with rigorously collected clinical data will become part of the Parkinson's Disease Biomarker Program (PDBP), providing valuable resources for biomarker development. Long-term observation of participants from these two trials, together comprising \ 600 early PD subjects, is invaluable not only in characterizing any persistent or delayed benefits of either randomized treatment but also in the development of tele-health outcomes to facilitate future interventional trials in PD and of neurotherapeutics more broadly. Challenges of traditional long-term follow up of large cohorts are the high cost of in-clinic assessment, the high dropout rates and the need to maintain multi-site infrastructure. The objective of this study is to leverage modern technology to develop, pilot and implement a 100% virtual model for long-term follow up utilizing telemedicine and smartphone platforms for quantitative monitoring of clinician- and patient-reported outcomes (PROs). This cohort may also serve to test feasibility of new technology platforms as they become available.

Interventions

None listed

Sponsors

Northwestern University
CollaboratorOTHER
Sage Bionetworks
CollaboratorOTHER
University of Rochester
CollaboratorOTHER
National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
Michael J. Fox Foundation for Parkinson's Research
CollaboratorOTHER
The Parkinson Study Group
CollaboratorNETWORK
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

1. Enrollment in STEADY-PD3 or SURE-PD3 studies 2. Prior consent to be contacted by the University of Rochester (UR) or if a participant from STEADY-PD III or SURE-PD3 studies directly contacts UR to request information about study participation 3. Internet-enabled device that will support participation in tele-visits 4. Have created or willing to create a Global Unique Identifier (GUID) 5. Willing and able to provide informed consent 6. English fluency 7. For participants opting to participate in the smartphone component, possession of a suitable smartphone (iPhone or Android) with adequate data plan and cellular network access/signal or wifi access

Exclusion criteria

1\. Inability to carry out study activities as determined by study staff

Design outcomes

Primary

MeasureTime frameDescription
Change in Tele-visit Modified MDS-UPDRS Parts 1-3 (Total Score)Two years (0, 12, and 24 months)Participants will be asked to complete (from home or other preferred environment) an hour-long Tele-visit that includes the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS), comprising MDS-UPDRS part 1a and (modified) part 3, as well as completion or confirmation of patient-reported component parts 1b and 2. The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse features. Parts I-III contain 59 total questions (13 in Part I, 13 in Part II, and 33 in Part III). Total scores are calculated as simple sums of component items with mean imputation by Part if no more than 1, 2, or 7 items are missing for Parts I through III, respectively. Total scores may range from 0 to 236, with 0 meaning no symptoms and 236 meaning worse symptoms.
Change in Tele-visit MDS-UPDRS Part 2 (Score)Two years (0, 12, and 24 months)The Movement Disorders Society Unified PD Rating Scale (MDS-UPDRS) Part II score comprises patient-reported responses to 13 questions on motor experiences of daily living. The response to each question is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Part II scores may range from a minimum of 0 to a maximum of 52, with higher values meaning worse symptoms.
Change in Smartphone Tapping (Score)Two years (0, 3, 6, 9, 12 , 15, 18, 21, and 24 months)The Smartphone Tapping Score is derived from a 30-second finger tapping task performed separately for each hand. The score ranges from 0 to 1 and higher scores are worse.
Change in Fox Insight MDS-UPDRS Part 2 (Score)Two years (0, 6, 12, 18, and 24 months)The Fox Insight MDS-UPDRS (Movement Disorders Society Unified PD Rating Scale) Part II score comprises patient-reported responses to 13 questions on motor experiences of daily living. Participants report their responses online through the Fox Insight web-based platform. The response to each question is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Part II scores may range from a minimum of 0 to a maximum of 52, with higher values meaning worse symptoms.

Secondary

MeasureTime frameDescription
Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)Two years (0, 3, 6, 9, 12, 15, 18, 21, and 24 months)The Non-motor Symptoms Questionnaire (NMS-QUEST) is a 30-question self-reported assessment. Each question is of a yes/no format with a score of 1 given to each yes answer, with total scores ranging from 0-30, with higher scores indicating a greater number of non-motor symptoms. Participants completed the assessment online in Fox Insight.
Change in Tele-visit Schwab and England (S&E; Score)Two years (0, 12, and 24 months)The Schwab and England scale is a Site Investigator and subject assessment of the subject's level of independence. The subject will be scored on a percentage scale reflecting his/her ability to perform acts of daily living. Printed scores with associated descriptors range from 0% to 100% in increments of 5%, with higher percentages associated with more independence. A score of 0% implies vegetative functions such as swallowing, bladder and bowel functions are not functioning; bedridden. A score of 100% implies subject has full ability and is completely independent; essentially normal.
Change in Tele-visit Clinician Global Impression - Severity (CGIS; Score)Two years (0, 12, and 24 months)The Clinician Global Impression (CGI) is an observer-rated scale that measures illness severity (CGIS). The CGIS is rated on a 7-point scale, with the severity of illness scale using a range of responses from 1 (normal) through 7 (amongst the most severely ill patients).
Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)Two years (0, 3, 6, 9, 12, 15, 18, 21, and 24 months)The Fox Insight PDQ-8 (Parkinson's Disease Questionnaire, short-form 8 item version) is a self-administered questionnaire used to measure quality of life in persons with Parkinson's disease. The response to each question is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Scores range from a minimum of 0 to a maximum of 32, with a higher score indicating a poorer quality of life.
Change in Tele-visit MDS-UPDRS Part 1a (Score)Two years (0, 12, and 24 months)Participants will be asked to complete (from home or other preferred environment) an hour-long Tele-visit that includes the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS), comprising MDS-UPDRS part 1a (i.e., the first six questions of part 1). The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse features. Part 1a scores may range from a minimum of 0 to a maximum of 24, with higher values meaning worse disability.
Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)Two years (0, 3, 6, 9, 12, 15, 18, 21, and 24 months)The Fox Insight Rapid Eye Movement Behavior Disorder (RBD) score is a patient-reported binary (no or yes) response to a single question of whether they act out their dreams while asleep. Participants report their response online through the Fox Insight web-based platform. The score value is dichotomous (or missing) and ranges from 0 (no symptom) to 1 (yes response).
Change in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score)Two years (0, 3, 9, 15, and 21 months)The Parkinson's Daily Activities Questionnaire -15 (PDAQ-15) is a 15-item measure of activities of daily living (ADL) that are impacted by cognitive impairment in participants with Parkinson's disease. The PDAQ-15 is derived from the original 50-item scale and is completed by the participant in Fox Insight. Scores range from 0 to 60, with higher scores indicating better function.
Change in Fox Insight Geriatric Depression Scale (GDS; Score)Two years (0, 12, and 24 months)The Geriatric Depression Scale (GDS) is a measure of depression completed by the participant online in Fox Insight. The scale has 30 yes/no questions, with each question having a maximum score of 1 and a total possible score ranging from 0 to 30. The higher the score, the greater the depression.
Change in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score)Two years (0, 6, 12, 18, and 24 months)The Fox Insight EQ-5D (European Quality of life survey) is a standardized measure of health-related quality of life assessing five dimensions of health. It comprises five corresponding questions on mobility, self-care, pain, usual activities, and psychological status with three possible answers for each item (1=no problem, 2=moderate problem, 3=severe problem). A derived summary index score is higher with better health-related quality of life. A maximum of 1 corresponds to the best quality of life, whereas a score of 0 is intended to approximate a state equivalent to death, with values less than 1 corresponding to a state worse than death.
Change in Tele-visit MDS-UPDRS Part 1b (Score)Two years (0, 12, and 24 months)The Movement Disorders Society Unified PD Rating Scale (MDS-UPDRS) Part Ib is the patient-reported portion of Part I, and assesses non-motor experiences of daily living. The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Part Ib contains 7 questions, and its scores may range from a minimum of 0 to a maximum of 28, with higher values meaning worse symptoms.
Change in Tele-visit Modified MDS-UPDRS Part 3 (Score)Two years (0, 12, and 24 months)Participants will be asked to complete (from home or other preferred environment) an hour-long Tele-visit that includes the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS), comprising MDS-UPDRS (modified) part 3. This measure omits 5 questions related to rigidity and 1 question related to postural instability, with a range from 0 to 108. The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse features.
Change in Tele-visit Montreal Cognitive Assessment (MoCA; Score)Two years (0, 12, and 24 months)The Montreal Cognitive Assessment (MoCA) assesses attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation. Points are awarded for the correct completion of MoCA tasks. Scores for each task are summed for a total score (range 0-30). Higher scores indicate greater cognitive capacity.

Countries

United States

Participant flow

Participants by arm

ArmCount
Former Phase 3 PD Trial Participants
The AT-HOME PD cohort enrolled upon completion of STEADY-PD3 or during completion of SURE-PD3; enrolling 2 to 6 years after diagnosis, and on standard dopaminergic therapy for 0 to 3 years. Former STEADY-PD3 participants had been randomized (1:1) to 3 years of isradipine or placebo treatment; SURE-PD3 participants had been randomized (1:1) to 2 years of inosine or placebo treatment.
226
Total226

Baseline characteristics

CharacteristicFormer Phase 3 PD Trial Participants
Age at diagnosis60.9 years
STANDARD_DEVIATION 8.9
Age at symptom onset59.4 years
STANDARD_DEVIATION 9.1
Age, Continuous64.7 years
STANDARD_DEVIATION 8.8
Clinician Global Impression - Severity
1 = Normal, not at all incapacitated
1 Participants
Clinician Global Impression - Severity
2 = Borderline incapacitated
60 Participants
Clinician Global Impression - Severity
3 = Mildly incapacitated
146 Participants
Clinician Global Impression - Severity
4 = Moderately incapacitated
19 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
6 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
220 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Fox Insight EQ-5D Score0.858 score on a scale
STANDARD_DEVIATION 0.132
Fox Insight GDS Score1.830 score on a scale
STANDARD_DEVIATION 2.348
Fox Insight MDS-UPDRS Part II Score7.978 score on a scale
STANDARD_DEVIATION 4.95
Fox Insight NMS-QUEST Score6.950 score on a scale
STANDARD_DEVIATION 4.136
Fox Insight PDAQ-15 Score55.444 score on a scale
STANDARD_DEVIATION 4.965
Fox Insight PDQ-8 Score2.927 score on a scale
STANDARD_DEVIATION 2.925
Fox Insight REM (Rapid Eye Movement) Behavior Disorder Score0.373 score on a scale
STANDARD_DEVIATION 0.487
Hoehn & Yahr1.8 units on a scale
STANDARD_DEVIATION 0.4
MDS-UPDRS Part I7.54 units on a scale
STANDARD_DEVIATION 4.84
MDS-UPDRS Part Ia1.46 units on a scale
STANDARD_DEVIATION 2.1
MDS-UPDRS Part Ib6.08 units on a scale
STANDARD_DEVIATION 3.4
MDS-UPDRS Part II8.60 units on a scale
STANDARD_DEVIATION 5.39
MDS-UPDRS Part III24.9 units on a scale
STANDARD_DEVIATION 11.5
MDS-UPDRS Part IV2.42 units on a scale
STANDARD_DEVIATION 3.15
MDS-UPDRS Parts I-III Total Score41.0 units on a scale
STANDARD_DEVIATION 16.5
MoCA total score27.9 units on a scale
STANDARD_DEVIATION 2
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
4 Participants
Race (NIH/OMB)
Black or African American
4 Participants
Race (NIH/OMB)
More than one race
2 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
215 Participants
Schwab & England Activities of Daily Living (ADL)89.7 units on a scale
STANDARD_DEVIATION 8.3
Sex: Female, Male
Female
90 Participants
Sex: Female, Male
Male
136 Participants
Smartphone Tapping (Score)0.627 score on a scale
STANDARD_DEVIATION 0.224
Use of antiparkinsonian medications
No
16 Participants
Use of antiparkinsonian medications
Yes
210 Participants
Use of levodopa
No
62 Participants
Use of levodopa
Yes
164 Participants
Years from diagnosis to baseline3.82 years
STANDARD_DEVIATION 1.19
Years from symptom onset to baseline5.30 years
STANDARD_DEVIATION 1.95

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 226
other
Total, other adverse events
1 / 226
serious
Total, serious adverse events
0 / 226

Outcome results

Primary

Change in Fox Insight MDS-UPDRS Part 2 (Score)

The Fox Insight MDS-UPDRS (Movement Disorders Society Unified PD Rating Scale) Part II score comprises patient-reported responses to 13 questions on motor experiences of daily living. Participants report their responses online through the Fox Insight web-based platform. The response to each question is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Part II scores may range from a minimum of 0 to a maximum of 52, with higher values meaning worse symptoms.

Time frame: Two years (0, 6, 12, 18, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight MDS-UPDRS Part 2 (Score)BL to Month 6-0.002 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight MDS-UPDRS Part 2 (Score)BL to Month 121.027 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight MDS-UPDRS Part 2 (Score)BL to Month 181.367 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight MDS-UPDRS Part 2 (Score)BL to Month 241.771 score on a scale
Comparison: Statistical analysis for BL to Month 6p-value: 0.996Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 12p-value: 0.054Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 18p-value: 0.025Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: 0.006Mixed Models Analysis
Primary

Change in Smartphone Tapping (Score)

The Smartphone Tapping Score is derived from a 30-second finger tapping task performed separately for each hand. The score ranges from 0 to 1 and higher scores are worse.

Time frame: Two years (0, 3, 6, 9, 12 , 15, 18, 21, and 24 months)

Population: Only subjects who consented and enrolled in the smartphone assessments are included in the analysis.

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 3-0.051 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 6-0.088 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 9-0.057 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 12-0.078 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 15-0.106 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 18-0.116 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 21-0.114 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Smartphone Tapping (Score)BL to Month 24-0.139 score on a scale
Comparison: Statistical analysis for BL to Month 3p-value: 0.007Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 6p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 9p-value: 0.004Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 12p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 15p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 18p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 21p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: <0.001Mixed Models Analysis
Primary

Change in Tele-visit MDS-UPDRS Part 2 (Score)

The Movement Disorders Society Unified PD Rating Scale (MDS-UPDRS) Part II score comprises patient-reported responses to 13 questions on motor experiences of daily living. The response to each question is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Part II scores may range from a minimum of 0 to a maximum of 52, with higher values meaning worse symptoms.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit MDS-UPDRS Part 2 (Score)BL to Month 120.575 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit MDS-UPDRS Part 2 (Score)BL to Month 241.550 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.011Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: <0.001Mixed Models Analysis
Primary

Change in Tele-visit Modified MDS-UPDRS Parts 1-3 (Total Score)

Participants will be asked to complete (from home or other preferred environment) an hour-long Tele-visit that includes the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS), comprising MDS-UPDRS part 1a and (modified) part 3, as well as completion or confirmation of patient-reported component parts 1b and 2. The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse features. Parts I-III contain 59 total questions (13 in Part I, 13 in Part II, and 33 in Part III). Total scores are calculated as simple sums of component items with mean imputation by Part if no more than 1, 2, or 7 items are missing for Parts I through III, respectively. Total scores may range from 0 to 236, with 0 meaning no symptoms and 236 meaning worse symptoms.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Modified MDS-UPDRS Parts 1-3 (Total Score)BL to Month 122.197 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Modified MDS-UPDRS Parts 1-3 (Total Score)BL to Month 248.943 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.006Mixed Models Analysis
p-value: <0.001Mixed Models Analysis
Secondary

Change in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score)

The Fox Insight EQ-5D (European Quality of life survey) is a standardized measure of health-related quality of life assessing five dimensions of health. It comprises five corresponding questions on mobility, self-care, pain, usual activities, and psychological status with three possible answers for each item (1=no problem, 2=moderate problem, 3=severe problem). A derived summary index score is higher with better health-related quality of life. A maximum of 1 corresponds to the best quality of life, whereas a score of 0 is intended to approximate a state equivalent to death, with values less than 1 corresponding to a state worse than death.

Time frame: Two years (0, 6, 12, 18, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score)BL to Month 6-0.010 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score)BL to Month 12-0.015 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score)BL to Month 180.003 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score)BL to Month 24-0.040 score on a scale
Comparison: Statistical analysis for BL to Month 6p-value: 0.595Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 12p-value: 0.44Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 18p-value: 0.909Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: 0.068Mixed Models Analysis
Secondary

Change in Fox Insight Geriatric Depression Scale (GDS; Score)

The Geriatric Depression Scale (GDS) is a measure of depression completed by the participant online in Fox Insight. The scale has 30 yes/no questions, with each question having a maximum score of 1 and a total possible score ranging from 0 to 30. The higher the score, the greater the depression.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Geriatric Depression Scale (GDS; Score)BL to Month 120.401 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Geriatric Depression Scale (GDS; Score)BL to Month 240.855 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.409Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 0.149p-value: 0.149Mixed Models Analysis
Secondary

Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)

The Non-motor Symptoms Questionnaire (NMS-QUEST) is a 30-question self-reported assessment. Each question is of a yes/no format with a score of 1 given to each yes answer, with total scores ranging from 0-30, with higher scores indicating a greater number of non-motor symptoms. Participants completed the assessment online in Fox Insight.

Time frame: Two years (0, 3, 6, 9, 12, 15, 18, 21, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 30.447 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 61.062 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 91.432 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 121.323 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 151.642 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 181.720 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 211.660 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score)BL to Month 242.046 score on a scale
Comparison: Statistical analysis for BL to Month 3p-value: 0.074Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 6p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 9p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 12p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 15p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 18p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 21p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: <0.001Mixed Models Analysis
Secondary

Change in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score)

The Parkinson's Daily Activities Questionnaire -15 (PDAQ-15) is a 15-item measure of activities of daily living (ADL) that are impacted by cognitive impairment in participants with Parkinson's disease. The PDAQ-15 is derived from the original 50-item scale and is completed by the participant in Fox Insight. Scores range from 0 to 60, with higher scores indicating better function.

Time frame: Two years (0, 3, 9, 15, and 21 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score)BL to Month 30.611 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score)BL to Month 9-0.798 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score)BL to Month 15-0.400 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score)BL to Month 21-1.618 score on a scale
Comparison: Statistical analysis for BL to Month 3p-value: 0.285Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 9p-value: 0.267Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 15p-value: 0.564Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 21p-value: 0.034Mixed Models Analysis
Secondary

Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)

The Fox Insight PDQ-8 (Parkinson's Disease Questionnaire, short-form 8 item version) is a self-administered questionnaire used to measure quality of life in persons with Parkinson's disease. The response to each question is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Scores range from a minimum of 0 to a maximum of 32, with a higher score indicating a poorer quality of life.

Time frame: Two years (0, 3, 6, 9, 12, 15, 18, 21, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 91.258 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 30.396 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 60.637 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 121.113 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 151.687 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 181.543 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 211.317 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score)BL to Month 241.744 score on a scale
Comparison: Statistical analysis for BL to Month 3p-value: 0.041Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 6p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 9p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 12p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 15p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 18p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 21p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: <0.001Mixed Models Analysis
Secondary

Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)

The Fox Insight Rapid Eye Movement Behavior Disorder (RBD) score is a patient-reported binary (no or yes) response to a single question of whether they act out their dreams while asleep. Participants report their response online through the Fox Insight web-based platform. The score value is dichotomous (or missing) and ranges from 0 (no symptom) to 1 (yes response).

Time frame: Two years (0, 3, 6, 9, 12, 15, 18, 21, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 3-0.125 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 6-0.008 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 90.020 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 120.088 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 15-0.117 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 180.148 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 210.003 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score)BL to Month 240.349 score on a scale
Comparison: Statistical analysis for BL to Month 3p-value: 0.2Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 6p-value: 0.888Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 9p-value: 0.837Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 12p-value: 0.394Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 15p-value: 0.268Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 18p-value: 0.039Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 21p-value: 0.979Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: 0.014Mixed Models Analysis
Secondary

Change in Tele-visit Clinician Global Impression - Severity (CGIS; Score)

The Clinician Global Impression (CGI) is an observer-rated scale that measures illness severity (CGIS). The CGIS is rated on a 7-point scale, with the severity of illness scale using a range of responses from 1 (normal) through 7 (amongst the most severely ill patients).

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Clinician Global Impression - Severity (CGIS; Score)BL to Month 120.103 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Clinician Global Impression - Severity (CGIS; Score)BL to Month 240.004 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.006Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: 0.937Mixed Models Analysis
Secondary

Change in Tele-visit MDS-UPDRS Part 1a (Score)

Participants will be asked to complete (from home or other preferred environment) an hour-long Tele-visit that includes the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS), comprising MDS-UPDRS part 1a (i.e., the first six questions of part 1). The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse features. Part 1a scores may range from a minimum of 0 to a maximum of 24, with higher values meaning worse disability.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit MDS-UPDRS Part 1a (Score)BL to Month 120.189 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit MDS-UPDRS Part 1a (Score)BL to Month 240.313 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.145Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: 0.029Mixed Models Analysis
Secondary

Change in Tele-visit MDS-UPDRS Part 1b (Score)

The Movement Disorders Society Unified PD Rating Scale (MDS-UPDRS) Part Ib is the patient-reported portion of Part I, and assesses non-motor experiences of daily living. The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse symptoms. Part Ib contains 7 questions, and its scores may range from a minimum of 0 to a maximum of 28, with higher values meaning worse symptoms.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit MDS-UPDRS Part 1b (Score)BL to Month 121.026 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit MDS-UPDRS Part 1b (Score)BL to Month 241.238 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: <0.001Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: <0.001Mixed Models Analysis
Secondary

Change in Tele-visit Modified MDS-UPDRS Part 3 (Score)

Participants will be asked to complete (from home or other preferred environment) an hour-long Tele-visit that includes the Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS), comprising MDS-UPDRS (modified) part 3. This measure omits 5 questions related to rigidity and 1 question related to postural instability, with a range from 0 to 108. The MDS-UPDRS is assessed on a 5-point Likert scale ranging from 0 to 4 where higher scores imply worse features.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Modified MDS-UPDRS Part 3 (Score)BL to Month 120.457 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Modified MDS-UPDRS Part 3 (Score)BL to Month 244.617 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.382Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: <0.001Mixed Models Analysis
Secondary

Change in Tele-visit Montreal Cognitive Assessment (MoCA; Score)

The Montreal Cognitive Assessment (MoCA) assesses attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation. Points are awarded for the correct completion of MoCA tasks. Scores for each task are summed for a total score (range 0-30). Higher scores indicate greater cognitive capacity.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Montreal Cognitive Assessment (MoCA; Score)BL to Month 12-0.051 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Montreal Cognitive Assessment (MoCA; Score)BL to Month 240.142 score on a scale
Comparison: Secondary analysis for BL to Month 12p-value: 0.688Mixed Models Analysis
Comparison: Secondary analysis for BL to Month 24p-value: 0.293Mixed Models Analysis
Secondary

Change in Tele-visit Schwab and England (S&E; Score)

The Schwab and England scale is a Site Investigator and subject assessment of the subject's level of independence. The subject will be scored on a percentage scale reflecting his/her ability to perform acts of daily living. Printed scores with associated descriptors range from 0% to 100% in increments of 5%, with higher percentages associated with more independence. A score of 0% implies vegetative functions such as swallowing, bladder and bowel functions are not functioning; bedridden. A score of 100% implies subject has full ability and is completely independent; essentially normal.

Time frame: Two years (0, 12, and 24 months)

ArmMeasureGroupValue (LEAST_SQUARES_MEAN)
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Schwab and England (S&E; Score)BL to Month 12-0.440 score on a scale
Former Phase 3 PD Trial ParticipantsChange in Tele-visit Schwab and England (S&E; Score)BL to Month 24-0.338 score on a scale
Comparison: Statistical analysis for BL to Month 12p-value: 0.446Mixed Models Analysis
Comparison: Statistical analysis for BL to Month 24p-value: 0.565Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026