Abstract

Abstract Introduction Wearable devices and mind-body interventions (MBIs) continue to receive widespread interest as tools for improving sleep. This study investigated the feasibility of using an automated electronic survey system and wearable heart rate (HR) monitor in the context of a fully remote clinical trial study to produce detailed measures of participant adherence, daily sleep quality, and associations with physiological outcomes captured by wearable devices. Methods Eighteen healthy participants (age 18-30yrs, 12 female) were randomized to one of three 8-week long interventions: slow-paced breathing (SPB, N=5, 24.6 ± 2.1 years, 4 female), mindfulness (M, N=6, 23.7 ± 3.7 years, 4 female), or yogic breathing (SPB+M, N=7, 24.3 ± 3.1 years). Participants completed two weeks of daily sleep logs prior to a virtual laboratory visit, consisting of a 60-min intervention-specific training with 20-min guided practice, and subsequent tasks including experimental stress induction. Participants started a 24-hour HR recording using a Polar H10 chest strap on the night prior. Then, participants were instructed to repeat their assigned intervention practice daily, using a guided audio similar to their initial training, while concurrently recording HR data and completing a detailed practice log. HR interbeat interval data were examined with spectral analysis using full spectrograms for inspection of timecourse and frequency-specific patterns in both the nocturnal recordings and daily practice sessions. Results Participants completed an average of 75% of daily practice sessions across the 8-week intervention period (SPB: 77%, M: 65%, SPB+M: 77%). An automated procedure was developed to analyze and visualize the timecourse of HRV-derived breathing patterns in the 754 completed practice sessions and 36 nocturnal recordings. The three groups were then successfully distinguishable based on breathing rates and mindfulness questionnaires. Nocturnal HR recordings demonstrated visually identifiable patterns of interindividual variability and intraindividual consistency. Statistical analysis is ongoing to further characterize these patterns. Conclusion These findings support feasibility for a fully remote, semi-automated clinical trial study assessing component-specific effects of these MBIs on sleep, including detailed spectral analysis of high-quality HR data. Future studies would benefit from examining scalability of this type of study design with wearable physiology in both clinical and nonclinical populations. Support (If Any) Pilot Research Grant, Osher Center for Integrative Medicine of Harvard Medical School and Brigham & Women’s Hospital; National Institutes of Health (5T32HL007901-22)

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