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Abstracts from the International Congress of Parkinson’s and Movement Disorders.

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Implementation of the Parkinson’s Disease-Health Index (PD-HI), a Novel, Validated, Disease-Specific Patient-Reported Outcome Measure, in a 24-Month Natural History Study

J. Purks, J. Seabury, J. Weinstein, A. Varma, S. Rosero, C. Engebrecht, C. Irwin, C. Shupe, A. Arky, J. Heatwole, C. Zizzi, N. Dilek, J. Adams, E. Dorsey, C. Heatwole (Rochester, USA)

Meeting: 2024 International Congress

Abstract Number: 486

Keywords: Parkinson’s, Scales

Category: Rating Scales

Objective: To evaluate and optimize the relevance, usability and longitudinal responsiveness of the Parkinson’s Disease-Health Index (PD-HI) for use in PD clinical trials.

Background: The use of valid, clinically relevant, and sensitive outcome measures is a priority of the FDA for PD therapeutic trials. In prior work, we developed and validated a disease-specific patient-reported outcome (PRO) measure known as the PD-HI. The present study is evaluating the PD-HI in a 24-month natural history study of PD to obtain longitudinal instrument metrics and optimize its current use for clinical trials and regulatory claims.

Method: We partnered with a variety of PD organizations (registries, foundations, support groups and clinics) to recruit an international cohort of adults with PD for a 24-month longitudinal study. Participants are completing the PD-HI, Neuro-QoL and the MDS-UPDRS parts 1b and 2 at baseline and every 6 months for a total of 24 months. Also, participants are completing a global impression of change questionnaire (6-24 months) and a survey preference form (baseline and 24 months). Statistical analysis will examine changes in PRO scores over time, the correlation of patient-reported disease progression with demographic and clinical characteristics and PD participant preferences for different PROs.

Results: 260 adults enrolled in the study and 206 participants completed at least one demographic survey question and one question on the PD-HI, meeting minimum threshold for data inclusion. A total of 149 participants completed all baseline survey assessments. To date, 114 participants have completed their 6-month assessment with all remaining 6-month assessments scheduled for completion by April 2024. Forthcoming longitudinal data will evaluate the PD-HI’s responsiveness to change and determine minimally clinically important difference values of the PD-HI and its subscales. This data will also assess how various PD symptomatic domains progress over time and identify which demographic and clinical characteristics are associated with a faster disease progression.

Conclusion: PD-HI is a 13-domain PRO that was designed and validated for use in PD clinical trials. Longitudinal evaluation of the PD-HI will further document its ability to track disease over time and quantify what constitutes a clinically meaningful change in its scores over time.

Summary of the PD-HI

Summary of the PD-HI

To cite this abstract in AMA style:

J. Purks, J. Seabury, J. Weinstein, A. Varma, S. Rosero, C. Engebrecht, C. Irwin, C. Shupe, A. Arky, J. Heatwole, C. Zizzi, N. Dilek, J. Adams, E. Dorsey, C. Heatwole. Implementation of the Parkinson’s Disease-Health Index (PD-HI), a Novel, Validated, Disease-Specific Patient-Reported Outcome Measure, in a 24-Month Natural History Study [abstract]. Mov Disord. 2024; 39 (suppl 1). https://www.mdsabstracts.org/abstract/implementation-of-the-parkinsons-disease-health-index-pd-hi-a-novel-validated-disease-specific-patient-reported-outcome-measure-in-a-24-month-natural-history-study/. Accessed June 15, 2025.
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