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Baseline results of a virtual longitudinal, observational study of Parkinson’s disease: The AT-HOME PD cohort

T. Myers, R. Schneider, L. Omberg, E. Macklin, E. Baloga, P. Snyder, S. Duquette, K. Amodeo, C. Tarolli, J. Adams, C. Lungu, J. Gottesman, E. Kayson, E. Dorsey, L. Mangravite, T. Simuni, M. Schwarzschild (Boston, MA, USA)

Meeting: MDS Virtual Congress 2020

Abstract Number: 923

Keywords: Parkinsonism

Category: Parkinson’s Disease: Clinical Trials

Objective: To describe the baseline characteristics of Parkinson’s disease (PD) clinical trial participants enrolled in a remote, long-term observational follow-up study.

Background: Participation in clinical research studies is cumbersome and assessments are often restricted to infrequent and time-consuming, in-clinic observation. Mobile and remote technologies may reduce participant burden, permit objective assessment in the home and result in new digital biomarkers of disease progression.

Method: Participants from two completed phase 3 clinical trials of potential disease-modifying therapeutics (SURE-PD3 and STEADY-PDIII) enrolled into AT-HOME PD. This 24-month observational study remotely characterizes long-term clinical outcomes through annual virtual research visits with a remote specialist. Optionally, participants complete quarterly two-week bursts of smartphone-based motor tasks and may opt into passive collection of GPS-based data (mPower). Additionally, participants may enroll in an online companion study, Fox Insight, and complete quarterly participant-reported outcome measures. In a sub-study, we are enrolling up to fifty individuals with PD from a separate on-going, longitudinal, observational study. Sub-study participants complete a single virtual research visit, which will establish the cross-sectional reliability of in-clinic versus virtual assessments (MoCA and MDS-UPDRS).

Results: From the two clinical trials, 350 individuals were pre-screened and 226 completed a baseline visit for AT-HOME PD (mean age (SD) of 64.3 (8.8) years, 39.8% female, 94% white) with participants located in 42 states and Canada. Of the optional study components, 72% of participants enrolled in Fox Insight and 81% in mPower. As of February 25, 2020, 12,714 smartphone-based motor tasks (mean (SD) 71.8 (74)/participant) have been completed with 57 individuals contributing passively collected data. The cohort has a mean (SD) modified MDS-UPDRS (AHPD-U01NS107009) part III score of 24.93 (11.50), Hoehn & Yahr of 1.79 (0.44), Schwab and England of 90.1% (5.6%), and MoCA score of 28 (1.9). Baseline virtual research visits were met with 97% satisfaction.

Conclusion: We successfully enrolled 45% of potentially eligible participants from the parent study cohorts into this long-term remote follow-up study, establishing the infrastructure for a new research model that is well accepted by participants.

To cite this abstract in AMA style:

T. Myers, R. Schneider, L. Omberg, E. Macklin, E. Baloga, P. Snyder, S. Duquette, K. Amodeo, C. Tarolli, J. Adams, C. Lungu, J. Gottesman, E. Kayson, E. Dorsey, L. Mangravite, T. Simuni, M. Schwarzschild. Baseline results of a virtual longitudinal, observational study of Parkinson’s disease: The AT-HOME PD cohort [abstract]. Mov Disord. 2020; 35 (suppl 1). https://www.mdsabstracts.org/abstract/baseline-results-of-a-virtual-longitudinal-observational-study-of-parkinsons-disease-the-at-home-pd-cohort/. Accessed June 15, 2025.
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