Why the study?
The study was conducted to determine the covariance of heart rate variability and self-reported neurobehavioral symptoms after traumatic brain injury collected using mobile health technology.
Does daily heart rate variability correlate with self-reported neurobehavioral symptoms in adults with and without traumatic brain injury?
Does daily heart rate variability correlate with self-reported neurobehavioral symptoms in adults with and without traumatic brain injury?
Remote collection of daily HRV and neurobehavioral symptoms is feasible, but the correlation between HRV and symptoms is highly individualized, requiring personalized interpretation.
Answers are grounded in this paper and cite their sources.
Variable same-day HRV-symptom correlations post-TBI; leaves open mHealth monitoring for personalized research.
Objectives: To determine the covariance of heart rate variability (HRV) and self-reported neurobehavioral symptoms after traumatic brain injury (TBI) collected using mobile health (mHealth) technology. Setting: Community. Participants: Adults with lifetime history of TBI ( n = 52) and adults with no history of brain injury ( n = 12). Design: Two-week prospective ecological momentary assessment study. Main Measures: Behavioral Assessment Screening Tool (BAST mHealth ) subscales (Negative Affect, Fatigue, Executive Dysfunction, Substance Abuse, and Impulsivity) measured frequency of neurobehavioral symptoms via a RedCap link sent by text message. Resting HRV (root mean square of successive R-R interval differences) was measured for 5 minutes every morning upon waking using a commercially available heart rate monitor (Polar H10, paired with Elite HRV app). Results: Data for n = 48 ( n = 38 with TBI; n = 10 without TBI) participants were included in covariance analyses, with average cross-correlation coefficients (0-day lag) varying greatly across participants. We found that the presence and direction of the relationship between HRV and neurobehavioral symptoms varied from person to person. Cross-correlation coefficients r ≤ −0.30, observed in 27.1% to 29.2% of participants for Negative Affect, Executive Dysfunction, and Fatigue, 22.9% of participants for Impulsivity, and only 10.4% of participants for Substance Abuse, supported our hypothesis that lower HRV would covary with more frequent symptoms. However, we also found 2.0% to 20.8% of participants had positive cross-correlations ( r ≥ 0.30) across all subscales, indicating that higher HRV may sometimes correlate with more neurobehavioral symptoms, and 54.2% to 87.5% had no significant cross-correlations. Conclusions: It is generally feasible for community-dwelling adults with and without TBI to use a commercially available wearable device to capture daily HRV measures and to complete a short, electronic self-reported neurobehavioral symptom measure for a 2-week period. The covariance of HRV and neurobehavioral symptoms over time suggests that HRV could be used as a relevant physiological biomarker of neurobehavioral symptoms, though how it would be interpreted and used in practice would vary on a person-by-person and symptom domain basis and requires further study.
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Nabasny et al. (2022) studied this question.
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