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myRhythmWatch

Evidence Tier:CLINICAL GRADE

Validated in clinical trials

For:Researchers & AcademicsClinicians & Healthcare ProfessionalsGeneral Public & Enthusiasts

App Summary

myRhythmWatch uses Apple Watch accelerometer data to help individuals, clinicians, and researchers assess and monitor 24-hour rest-activity rhythms, which are linked to various health outcomes including cognitive impairment. A preliminary pilot study (N=40) established the platform's feasibility in older adults with and without mild cognitive impairment, finding that more fragmented rhythms were associated with worse processing speed. The associated research concludes that this system provides a feasible and scalable approach for characterizing health risk factors, supporting its use in future clinical trials and for personal health awareness.

App Screenshots

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Detailed Description

Functionality & Mechanism

myRhythmWatch is a mobile health platform developed for the passive quantification of 24-hour rest-activity rhythms (RARs). The system captures raw accelerometer data through a continuously worn Apple Watch for a minimum of three days. This data is synchronized via HealthKit and Bluetooth to a web-based service where nonparametric and extended-cosine RAR variables are computed. The interface then visualizes these metrics, providing a longitudinal assessment of rhythm stability, amplitude, and fragmentation to facilitate rhythm monitoring.

Evidence & Research Context

  • A validation study (N=23) comparing Apple Watch data to a research-grade ActiGraph device demonstrated good-to-excellent consistency (ICC=0.84) and strong correlations (Spearman R=0.7–0.9) for key rest-activity rhythm metrics.
  • A pilot feasibility study (N=40) in older adults, including individuals with mild cognitive impairment (MCI), confirmed the system is a viable and acceptable tool for longitudinal data collection in this population.
  • In the same pilot study, specific rhythm characteristics, such as fragmentation and activity onset timing, were significantly associated with neuropsychological performance on memory and processing speed tasks.
  • The platform was designed to provide a scalable, real-time method for circadian rhythm assessment, addressing the practical limitations of traditional actigraphy for large-scale research and clinical applications.

Intended Use & Scope

This platform is intended for researchers and clinicians for the longitudinal assessment of rest-activity rhythms. It serves as a tool for risk factor characterization and monitoring, not for clinical diagnosis. The derived metrics are device-specific and should not be directly compared with values from other actigraphy systems. Interpretation requires professional context and is not a substitute for clinical evaluation.

Studies & Publications

3 publications

Peer-reviewed research associated with this app.

Validation Study

Comparison of rest-activity rhythm metrics from apple watch and ActiGraph devices

Zhang et al. (2025) · Sleep

Apple Watch measurements showed good-to-excellent consistency with ActiGraph for rest-activity rhythm monitoring.

Abstract Study Objectives Objective rest–activity rhythm (RAR) disturbances are linked with major disease outcomes. If consumer wearables yield RAR measures comparable to traditional research devices, these popular devices could provide a scalable option for clinical applications of RAR monitoring, e.g. risk factor screening. Methods We asked a convenience sample of participants (analytic n = 23; mean age = 27 years; 80% female) to wear Apple
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Pilot/Feasibility Study

Detecting Sleep/Wake Rhythm Disruption Related to Cognition in Older Adults With and Without Mild Cognitive Impairment Using the myRhythmWatch Platform: Feasibility and Correlation Study

Jones et al. (2025) · JMIR Aging

Successfully collected sufficient sleep/wake rhythm data from all participants using consumer wearables.

Abstract Background Consumer wearable devices could, in theory, provide sufficient accelerometer data for measuring the 24-hour sleep/wake risk factors for dementia that have been identified in prior research. To our knowledge, no prior study in older adults has demonstrated the feasibility and acceptability of accessing sufficient consumer wearable accelerometer data to compute 24-hour sleep/wake rhythm measures. Objective We aimed to establish
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myRhythmWatch

Free