As Parkinson's disease (PD) is a heterogeneous disorder, personalized medicine is truly required to optimize care. In their current form, standard scores from paper and pencil symptom-measures traditionally used to track disease progression are too coarse (discrete) to capture the granularity of the clinical phenomena under consideration, in the face of tremendous symptom diversity. For this reason, sensors, wearables, and mobile devices are increasingly incorporated into PD research and routine care. These digital measures, while more precise, yield data that are less standardized and interpretable than traditional measures, and consequently, the two types of data remain largely siloed. Both of these issues present barriers to the broad clinical application of the field's most precise assessment tools. This protocol addresses both problems. Using traditional tasks to measure cognition and motor control, we test the participant, while co-registering biophysical signals unobtrusively using wearables. We then integrate the scores from traditional paper-and-pencil methods with the digital data that we continuously register. We offer a new standardized data type and unifying statistical platform that enables the dynamic tracking of change in the person's stochastic signatures under different conditions that probe different functional levels of neuromotor control, ranging from voluntary to autonomic. The protocol and standardized statistical framework offer dynamic digital biomarkers of physical and cognitive function in PD that correspond to validated clinical scales, while significantly improving their precision. Video Link The video component of this article can be found at https://www.jove.com/video/59827/ 4. Among those are the disparity in the data that is acquired, namely discrete scores from clinical pencil-and-paper methods guided by observation, and continuous biophysical data physically acquired from the nervous systems output (e.g., using biosensors). The data from clinical scores tend to assume a one-size-fits all static model that enforces a single (theoretical) probability distribution function (PDF). This a priori assumption is imposed on the data without proper empirical validation, because normative data has not been acquired and characterized in the first place. As such, there is no proper similarity-metric-based criteria describing the neurotypical maturational states of the human nervous systems, as the healthy person ages and the probability spaces used to cast these parameter variations shift at some rate. Without normative data and proper similarity metrics, it is not possible to measure departures from typical states as they dynamically change across the person's life. It is also not possible to predict the sensory consequences of the upcoming changes.