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. 2022 Jun 20;23:518. doi: 10.1186/s13063-022-06444-0

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.

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Fig. 3 — Clinical trial timeline. Participants are recruited as inpatients shortly after a stroke or as outpatients after hospital discharge. After a pre-selection, participants receive baseline evaluations and are randomly assigned to the intervention group or control group. The inpatients start using the RGS desktop setup during their stay at the hospital, while the outpatients use RGS directly in their homes. All participants in the intervention group are provided with a wearable device (RGSwear) for continuous monitoring. The control group receives rehabilitation as usual according to the standard care of the countries included in the study. According to the outcome measures assessments, all participants are evaluated again at 3, 6, and 12 months after baseline evaluation (see Tables 2 and 3)