Garmin HRV Accuracy: How Enhanced BBI Resolves Systematic Bias in Nightly HRV

Garmin HRV Accuracy: How Enhanced BBI Resolves Systematic Bias in Nightly HRV

Recent studies identified accuracy concerns with Garmin HRV measurements from older devices. Our validation research demonstrates that Garmin's Enhanced BBI technology completely resolves these issues, providing research-grade data quality on newer devices.

Feb 11, 2026
By Dr. Han-Ping Huang
Garmin HRV Accuracy

Introduction

Heart Rate Variability (HRV), and specifically the root mean square of successive differences (RMSSD), remains a cornerstone metric for assessing autonomic nervous system function, stress, and recovery.

In our previous article, Demystifying Garmin’s Enhanced BBI, we demonstrated that Garmin’s Enhanced Beat-to-Beat Intervals (eBBI) deliver near-ECG accuracy during low-motion conditions. We showed how eBBI preserves critical high-frequency components - such as respiratory sinus arrhythmia (RSA) - and provides per-beat confidence flags that reliably reflect signal quality.

Building on those insights, this article addresses a critical concern raised in recent validation studies: the presence of systematic biases in legacy Garmin-derived nightly RMSSD when compared to ECG reference data.

Key Findings:

  • Legacy Garmin BBI: shows systematic bias: overestimates low RMSSD, underestimates high RMSSD
  • Enhanced BBI (eBBI): eliminates this non-linear bias pattern
  • Physiological Offset: remaining +8ms offset is physiological (PRV vs HRV), not algorithmic error
  • Research Grade: Gen 4+ Garmin devices with eBBI deliver research-grade HRV accuracy

The Challenge: Reported Bias in Legacy Garmin HRV

A 2025 validation study compared nocturnal resting heart rate and HRV across five wearable devices against a Polar H10 ECG reference [1]. While devices like Oura Ring (Gen 3/4), Whoop, and Polar Grit showed differences distributed around zero in Bland-Altman analyses, the Garmin Fenix 6 exhibited a distinctive, problematic pattern (Fig. 1):

  • Overestimation when true RMSSD was low
  • Underestimation when true RMSSD was high.

This systematic bias raised valid questions regarding the reliability of legacy Garmin data for precise autonomic monitoring, prompting researchers to seek clarification [2].

Bland-Altman plot showing Garmin Fenix 6 systematic RMSSD bias compared to Oura Ring Gen 3 accuracy against Polar H10 ECG
Fig. 1. Comparison of systematic error profiles reported in previous literature. Bland-Altman plots adapted from [1] comparing average nightly RMSSD against a Polar H10 ECG reference. (a) The Garmin Fenix 6 exhibits a distinct bias pattern: overestimation at low RMSSD and underestimation at high RMSSD. (b) The Oura Ring (Gen 3) shows differences centered around zero, indicating no systematic bias across the physiological range.

Independent Validation: Legacy vs. Enhanced BBI

To investigate this, Labfront conducted a month-long overnight data collection study using a Garmin Venu 3 worn simultaneously with a validated chest-based ECG device (Movesense). Our dataset included:

  • Ground Truth: ECG-derived R-R intervals (RRI).
  • Legacy Data: Garmin legacy BBI and official 5-minute RMSSD from Garmin Connect (GC).
  • Enhanced Data: Garmin Enhanced BBI (eBBI) with per-beat confidence flags.

We calculated average 5-minute RMSSD values during sleep to match the protocol of the original validation study and performed Bland-Altman analyses.

1. Results with Legacy BBI

Our analysis confirmed the findings of the 2025 study. Both the Garmin Connect RMSSD and RMSSD derived from legacy BBI replicated the reported bias: positive differences at low variability and negative differences at high variability (Fig.2).

The cause: The underestimation at high RMSSD values aligns with known processing limitations in legacy BBI. To maximize data availability, legacy algorithms applied bandwidth-limiting filters [2]. While effective for stability, these filters inadvertently suppressed large beat-to-beat fluctuations, artificially lowering RMSSD during periods of high autonomic variability.

2. Results with Enhanced BBI

When the same dataset was processed using Enhanced BBI (eBBI) - filtering out low-confidence beats and requiring 70–90% high-confidence coverage per 5-minute window - the results changed dramatically.

The pattern of systematic bias disappeared. The Bland-Altman distribution became flat, showing no systematic underestimation across the entire RMSSD range (Fig.2).

Comparison of RMSSD bias in Garmin Connect, legacy BBI, and Enhanced BBI versus ECG reference showing elimination of systematic bias
Fig. 2. Impact of Enhanced BBI on systematic bias. Bland-Altman analysis from our independent validation comparing average 5-minute nocturnal RMSSD against an ECG reference (Movesense). (a) Official Garmin Connect (GC) values replicate the systematic bias pattern observed in the original validation study. (b) RMSSD derived directly from legacy BBI exhibits an identical error profile, confirming that official GC metrics rely on legacy processing. (c) RMSSD derived from Enhanced BBI (eBBI) with quality filtering eliminates the non-linear bias; differences are uniformly distributed around a mean offset of ≈+8 ms, with no systematic dependence on RMSSD magnitude.

A New Observation: The Physiological “Positive Offset”

While the non-linear bias was resolved, eBBI-derived RMSSD exhibited a consistent positive offset relative to the ECG reference (mean difference ≈+8 ms) (Fig.2c).

We hypothesize that the "overestimation at low RMSSD" reported in previous literature is actually a misinterpretation of this phenomenon. Unlike the legacy "bandwidth limiting" issue, this positive offset is not a processing error; rather, it appears to be a physiological characteristic of measuring Pulse Rate Variability (PRV) at the wrist versus Heart Rate Variability (HRV) at the chest.

Investigating the Signal Source

To understand this offset, we examined the underlying raw PPG signal. We collected raw PPG from a Biostrap device worn on the same wrist to serve as a proxy for the optical conditions encountered by the Garmin sensor.

  • Stable Conditions: When the PPG signal was perfectly stable, legacy BBI and eBBI closely matched the ECG RRI (Fig.3).
  • Baseline Wander: When the PPG signal exhibited low-frequency baseline drift—often driven by respiration - Garmin eBBI showed greater short-term fluctuation amplitude than the ECG even during high-confidence periods with stable sensor contact (Fig.4).

Beat-to-beat interval alignment during stable PPG conditions showing ECG, legacy BBI, and Enhanced BBI comparison
Fig. 3. Signal alignment during stable PPG conditions. Representative 45-second epoch from overnight data. (a) Beat-to-beat intervals from ECG RRI (blue), Garmin legacy BBI (green), and Enhanced BBI (red). (b) Biostrap raw PPG (red) overlaid with high-pass filtered PPG (green) and detected pulse peaks (circles). During stable conditions—where raw and filtered waveforms largely overlap—both legacy and enhanced BBI align closely with ECG RRI. Note the deviation in legacy BBI between 00:52:30 and 00:52:47; this illustrates how legacy bandwidth-limiting filters suppress large beat-to-beat fluctuations and introduce timing shifts, even when signal quality is high.

Impact of respiratory baseline drift on pulse rate variability in Enhanced BBI versus ECG showing physiological differences
Fig. 4. Impact of low-frequency baseline drift on interval variability. Representative 35-second epoch from overnight data. (a) Beat-to-beat intervals from ECG RRI (blue), Legacy BBI (green), and Enhanced BBI (red). (b) Biostrap raw PPG (red) versus high-pass filtered PPG (green) with detected pulse peaks (vertical markers). Pronounced low-frequency drift is visible where the raw and filtered waveforms diverge significantly. During these periods (notably 02:39:25–02:39:30 and 02:39:38–02:39:45), eBBI exhibits greater short-term fluctuation amplitude than ECG RRI, illustrating how respiratory-driven baseline wander modulates pulse peak timing at the wrist.

The Role of Pulse Transit Time (PTT)

This additional variability is physiological. Respiration affects not only the heart rate (RSA) but also intrathoracic pressure, venous return, and blood pressure. These factors modulate Pulse Transit Time (PTT) - the time it takes for the pulse wave to travel from the heart to the wrist.

Because PPG measures the mechanical arrival of the pulse (which is delayed by variable PTT), it inherently contains more variability than the electrical excitation measured by ECG. This phenomenon results in PPG-derived RMSSD being systematically higher than ECG-derived RMSSD, a finding corroborated by separate 2025 studies comparing Polar H10 (ECG) with Polar OH1 (arm-based PPG) [3].

Implications for HRV Research

These findings are convincingly positive for researchers utilizing Garmin devices:

  1. Enhanced BBI Resolves the Reported Primary Bias: The problematic pattern of underestimating high RMSSD seen in legacy systems is eliminated with eBBI.
  2. The Offset is Physiological: The remaining positive offset reflects real physiological differences between optical wrist sensing (PRV) and electrical chest sensing (HRV), rather than algorithmic failure.
  3. Quality Control is Critical: As highlighted in our previous work, the key to research-grade data is excluding low-confidence beats.

For researchers concerned about earlier validation studies, the solution is straightforward: Use Enhanced BBI on Gen 4+ Garmin sensors and apply confidence-based quality filters.

Conclusion: Enhanced BBI Elevates Wearable HRV to Research-Grade Reliability

The analysis presented here confirms that the transition from legacy BBI to Enhanced BBI significantly mitigates the systematic biases previously reported in Garmin-derived nightly RMSSD. eBBI yields data that more closely mirrors raw pulse peak intervals, distinguishing physiological Pulse Rate Variability from algorithmic artifacts. When combined with Labfront’s seamless integration - offering automatic syncing, confidence-based filtering, and advanced analytics - researchers can confidently deploy Garmin devices for precise studies. 

For the research community, these findings emphasize the importance of data granularity over pre-calculated metrics. Platforms like Labfront facilitate access to these raw intervals and confidence flags, enabling investigators to apply independent quality control criteria essential for rigorous analysis. Consequently, when appropriate filtering is applied to Enhanced BBI data, modern Garmin sensors offer a viable, scalable alternative to chest-based ECG for longitudinal autonomic monitoring.

Get research-grade HRV data from Garmin devices!

Labfront gives you access to validated Enhanced BBI with automatic quality filtering.

FAQ

Yes, when using Enhanced BBI on Gen 4+ Garmin devices. Our validation study shows that Enhanced BBI eliminates the systematic bias present in legacy systems and delivers research-grade accuracy. The remaining offset is physiological (PRV vs HRV) rather than a measurement error.
Enhanced BBI (Beat-to-Beat Intervals) is Garmin's advanced processing algorithm that provides near-ECG accuracy for heart rate variability measurements. Unlike legacy BBI, it includes per-beat confidence flags and preserves high-frequency components like respiratory sinus arrhythmia without bandwidth-limiting filters.
Wrist-based optical sensors (PPG) measure Pulse Rate Variability (PRV), while chest straps measure Heart Rate Variability (HRV) from electrical signals. PRV includes additional physiological variability from Pulse Transit Time—the time it takes for the pulse wave to travel from heart to wrist. This results in slightly higher RMSSD values (typically +8ms) and is a normal physiological difference, not an error.
Enhanced BBI is available on Gen 4 and newer Garmin devices. Check our most current list of compatible devices here.
HRV (Heart Rate Variability) measures variation in electrical signals from the heart, typically via ECG. PRV (Pulse Rate Variability) measures variation in mechanical pulse arrival at peripheral sites like the wrist, using optical sensors. PRV includes both cardiac variability and vascular transit time variability, making it slightly higher but still highly correlated with HRV.

Reference

  1. Dial, M. B., Hollander, M. E., Vatne, E. A., Emerson, A. M., Edwards, N. A., & Hagen, J. A. (2025). Validation of nocturnal resting heart rate and heart rate variability in consumer wearables. Physiological reports, 13(16), e70527. https://doi.org/10.14814/phy2.70527
  2. www8.garmin.com/garminhealth/news/Garmin-Enhanced-BBI_Final.pdf 
  3. Miller, D. J., Sargent, C., & Roach, G. D. (2022). A Validation of Six Wearable Devices for Estimating Sleep, Heart Rate and Heart Rate Variability in Healthy Adults. Sensors (Basel, Switzerland), 22(16), 6317. https://doi.org/10.3390/s22166317
  4. Coste, A., Millour, G., & Hausswirth, C. (2025). A Comparative Study Between ECG- and PPG-Based Heart Rate Sensors for Heart Rate Variability Measurements: Influence of Body Position, Duration, Sex, and Age. Sensors (Basel, Switzerland), 25(18), 5745. https://doi.org/10.3390/s25185745
Dr. Han-Ping Huang, PhD
Dr. Han-Ping Huang, PhD
Research Lead

Han-Ping is the senior research lead (and chief plant caretaker) at Labfront, specializing in physiological data analysis. An alumnus of the BIDMC/Harvard's Center for Dynamical Biomarkers, Han-Ping uses his PhD in electrophysics to help Labfront customers convert raw physiological data into health insights. He does his best Python coding while powered by arm massages from his spiky-tongued cat, Pi.

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