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. 2018 Dec 20;18:138. doi: 10.1186/s12911-018-0714-7

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — The four remote protocol compliance metrics tracked in this report using the Intel® Pharma Analytics Platform with their associated smartphone application screenshots. a The PD trial tracked three metrics as defined by the study protocol: app-based medication reporting of the patient’s normal, predefined medication regimen, smartwatch data streaming excluding charging time, and app-based daily symptoms reporting. b The HD trial tracked four compliance measures as defined by the study protocol: app-based medication reporting of the investigational drug, daily smartwatch data streaming excluding charging time, app-based daily symptoms reporting, and performance of structured motor assessments at home. The smartwatch graphic was obtained from Wikimedia Commons