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Smartwach Actigraphy for Detection of REM Sleep Behavior Disorder: The dBM-DEV Study

N. Schnalke, T. Feige, J. Zaras, C. Chatzichristos, F. Wang, M. de Vos, I. Gerasimou, A. Moustaklis, N. Del Campo, M. Fabbri, R. Debs, M. Almarcha-Menargues, M. Kurtis, O. Sanchez-Solino, D. Matzakou-Karvouniari, A. Mioglou, C. Sotirakis, L. Hadjileontiadis, S. Hadjidimitriou, B. Falkenburger (Dresden, Germany)

Meeting: 2026 International Congress

Keywords: Parkinson’s, Rapid eye movement(REM), Synucleinopathies

Category: Parkinson's disease: Biomarkers (non-Neuroimaging)

Objective: To evaluate feasibility and performance of multi-night at-home recordings using a smartwatch to (1) detect REM sleep behavior disorder (RBD) compared with polysomnography (PSG) and (2) assess performance relative to a screening questionnaire (REM Sleep Behavior Disorder Screening Questionnaire; RBDSQ).

Background: RBD is a prodromal manifestation of Parkinson’s disease (PD) and other synucleinopathies. Identification RBD relies on PSG, which is typically limited to one or two nights despite substantial night-to-night variability of symptoms. Accessible and reliable approaches for longitudinal screening are needed. This study is part of AI-PROGNOSIS, a research project funded by the European Union (Grant Agreement No. 101080581).

Method: The digital biomarkers development study (dBM-DEV) recruited 81 participants across three European sites (Germany, Spain, France). The development cohort included 29 participants with PSG-confirmed RBD (27 idiopathic RBD [iRBD], 2 PD with RBD) and 24 controls. The confirmation cohort included 28 PD participants with unknown RBD status. Participants wore a smartwatch nightly for up to three months. PD participants underwent PSG. RBD-associated features were extracted, and machine-learning algorithms were developed for subject-level RBD detection. In PD participants, smartwatch-derived digital biomarker (dBM) results were compared with RBDSQ (cut-off ≥6) and one-night PSG.

Results: Controls and iRBD participants in the development cohort were classified with high accuracy using seven nights of data (88%, XGBoost). In the confirmation cohort, 22 of 23 PD participants with sufficient smartwatch data were classified as dBM-positive. PSG was performed in 24 PD participants. Of 16 conclusive PSGs, 13 were RBD-positive and 3 RBD-negative, while 8 were inconclusive. The observed PSG-based RBD prevalence in PD was 81%. The pre-specified endpoint (higher specificity of dBMs vs RBDSQ) was inconclusive due to too few PSG-negative cases. Sensitivity was not statistically different (dBM 91% vs RBDSQ 100%).

Conclusion: Multi-night smartwatch recordings are feasible and show high sensitivity for RBD detection in real-world settings. The high prevalence of RBD in PD participants and frequent inconclusive single-night PSG findings support longitudinal dBM assessments, which may aid identification of individuals with RBD for clinical trials. Further studies are needed to test the specificity of dBMs.

To cite this abstract in AMA style:

N. Schnalke, T. Feige, J. Zaras, C. Chatzichristos, F. Wang, M. de Vos, I. Gerasimou, A. Moustaklis, N. Del Campo, M. Fabbri, R. Debs, M. Almarcha-Menargues, M. Kurtis, O. Sanchez-Solino, D. Matzakou-Karvouniari, A. Mioglou, C. Sotirakis, L. Hadjileontiadis, S. Hadjidimitriou, B. Falkenburger. Smartwach Actigraphy for Detection of REM Sleep Behavior Disorder: The dBM-DEV Study [abstract]. Mov Disord. 2026; 41 (suppl 1). https://www.mdsabstracts.org/abstract/smartwach-actigraphy-for-detection-of-rem-sleep-behavior-disorder-the-dbm-dev-study/. Accessed October 1, 2026.
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