Parkinson Disease
Conditions
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
Study design
Eligibility
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
| Measure | Time frame | Description |
|---|---|---|
| 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
| Measure | Time frame | Description |
|---|---|---|
| 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
| Arm | Count |
|---|---|
| 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 |
| Total | 226 |
Baseline characteristics
| Characteristic | Former Phase 3 PD Trial Participants |
|---|---|
| Age at diagnosis | 60.9 years STANDARD_DEVIATION 8.9 |
| Age at symptom onset | 59.4 years STANDARD_DEVIATION 9.1 |
| Age, Continuous | 64.7 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 Score | 0.858 score on a scale STANDARD_DEVIATION 0.132 |
| Fox Insight GDS Score | 1.830 score on a scale STANDARD_DEVIATION 2.348 |
| Fox Insight MDS-UPDRS Part II Score | 7.978 score on a scale STANDARD_DEVIATION 4.95 |
| Fox Insight NMS-QUEST Score | 6.950 score on a scale STANDARD_DEVIATION 4.136 |
| Fox Insight PDAQ-15 Score | 55.444 score on a scale STANDARD_DEVIATION 4.965 |
| Fox Insight PDQ-8 Score | 2.927 score on a scale STANDARD_DEVIATION 2.925 |
| Fox Insight REM (Rapid Eye Movement) Behavior Disorder Score | 0.373 score on a scale STANDARD_DEVIATION 0.487 |
| Hoehn & Yahr | 1.8 units on a scale STANDARD_DEVIATION 0.4 |
| MDS-UPDRS Part I | 7.54 units on a scale STANDARD_DEVIATION 4.84 |
| MDS-UPDRS Part Ia | 1.46 units on a scale STANDARD_DEVIATION 2.1 |
| MDS-UPDRS Part Ib | 6.08 units on a scale STANDARD_DEVIATION 3.4 |
| MDS-UPDRS Part II | 8.60 units on a scale STANDARD_DEVIATION 5.39 |
| MDS-UPDRS Part III | 24.9 units on a scale STANDARD_DEVIATION 11.5 |
| MDS-UPDRS Part IV | 2.42 units on a scale STANDARD_DEVIATION 3.15 |
| MDS-UPDRS Parts I-III Total Score | 41.0 units on a scale STANDARD_DEVIATION 16.5 |
| MoCA total score | 27.9 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 baseline | 3.82 years STANDARD_DEVIATION 1.19 |
| Years from symptom onset to baseline | 5.30 years STANDARD_DEVIATION 1.95 |
Adverse events
| Event type | EG000 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
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Fox Insight MDS-UPDRS Part 2 (Score) | BL to Month 6 | -0.002 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight MDS-UPDRS Part 2 (Score) | BL to Month 12 | 1.027 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight MDS-UPDRS Part 2 (Score) | BL to Month 18 | 1.367 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight MDS-UPDRS Part 2 (Score) | BL to Month 24 | 1.771 score on a scale |
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.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 3 | -0.051 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 6 | -0.088 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 9 | -0.057 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 12 | -0.078 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 15 | -0.106 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 18 | -0.116 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 21 | -0.114 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Smartphone Tapping (Score) | BL to Month 24 | -0.139 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit MDS-UPDRS Part 2 (Score) | BL to Month 12 | 0.575 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit MDS-UPDRS Part 2 (Score) | BL to Month 24 | 1.550 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit Modified MDS-UPDRS Parts 1-3 (Total Score) | BL to Month 12 | 2.197 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit Modified MDS-UPDRS Parts 1-3 (Total Score) | BL to Month 24 | 8.943 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change 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 Participants | Change 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 Participants | Change in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score) | BL to Month 18 | 0.003 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight EuroQol Five Dimensions Questionnaire (EQ-5D; Score) | BL to Month 24 | -0.040 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Fox Insight Geriatric Depression Scale (GDS; Score) | BL to Month 12 | 0.401 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Geriatric Depression Scale (GDS; Score) | BL to Month 24 | 0.855 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 3 | 0.447 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 6 | 1.062 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 9 | 1.432 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 12 | 1.323 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 15 | 1.642 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 18 | 1.720 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 21 | 1.660 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Non-motor Symptoms Questionnaire (NMS-QUEST; Score) | BL to Month 24 | 2.046 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score) | BL to Month 3 | 0.611 score on a scale |
| Former Phase 3 PD Trial Participants | Change 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 Participants | Change 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 Participants | Change in Fox Insight Parkinson's Daily Activities Questionnaire -15 (PDAQ-15; Score) | BL to Month 21 | -1.618 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 9 | 1.258 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 3 | 0.396 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 6 | 0.637 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 12 | 1.113 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 15 | 1.687 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 18 | 1.543 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 21 | 1.317 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight Parkinson's Disease Questionnaire - 8 Item Version (PDQ-8; Score) | BL to Month 24 | 1.744 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change 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 Participants | Change 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 Participants | Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score) | BL to Month 9 | 0.020 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score) | BL to Month 12 | 0.088 score on a scale |
| Former Phase 3 PD Trial Participants | Change 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 Participants | Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score) | BL to Month 18 | 0.148 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score) | BL to Month 21 | 0.003 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Fox Insight REM (Rapid Eye Movement) Behavior Disorder (RBD; Score) | BL to Month 24 | 0.349 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit Clinician Global Impression - Severity (CGIS; Score) | BL to Month 12 | 0.103 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit Clinician Global Impression - Severity (CGIS; Score) | BL to Month 24 | 0.004 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit MDS-UPDRS Part 1a (Score) | BL to Month 12 | 0.189 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit MDS-UPDRS Part 1a (Score) | BL to Month 24 | 0.313 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit MDS-UPDRS Part 1b (Score) | BL to Month 12 | 1.026 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit MDS-UPDRS Part 1b (Score) | BL to Month 24 | 1.238 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit Modified MDS-UPDRS Part 3 (Score) | BL to Month 12 | 0.457 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit Modified MDS-UPDRS Part 3 (Score) | BL to Month 24 | 4.617 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit Montreal Cognitive Assessment (MoCA; Score) | BL to Month 12 | -0.051 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit Montreal Cognitive Assessment (MoCA; Score) | BL to Month 24 | 0.142 score on a scale |
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)
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Former Phase 3 PD Trial Participants | Change in Tele-visit Schwab and England (S&E; Score) | BL to Month 12 | -0.440 score on a scale |
| Former Phase 3 PD Trial Participants | Change in Tele-visit Schwab and England (S&E; Score) | BL to Month 24 | -0.338 score on a scale |