Comparison of Heart Rate Variability Analysis Durations and Their Relationship With Blood Pressure

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorSinop University

About this trial

This observational study aims to compare heart rate variability (HRV) parameters obtained from different analysis durations in healthy adults and to examine how these parameters relate to resting blood pressure values. HRV is a noninvasive measure commonly used to assess autonomic nervous system activity. Standard short-term HRV analysis is typically based on 5-minute recordings, but shorter and longer analysis durations are also used in research and practice. This study will evaluate whether HRV values derived from 1-minute, 5-minute, 10-minute, and 20-minute analysis windows differ from one another and whether their relationships with systolic blood pressure, diastolic blood pressure, and mean arterial pressure change according to analysis duration. Participants will attend a single study visit. After a rest period, resting blood pressure and pulse will be measured, and a continuous HRV recording will be obtained using a chest strap device. The study is designed to provide methodological information on the comparability of different HRV analysis durations under the same physiological conditions.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy adults aged 18 to 40 years

Willing and able to provide informed consent

Able to comply with pre-assessment instructions, including restrictions related to caffeine intake and strenuous physical activity

No condition preventing heart rate variability and blood pressure measurements

Disqualifiers

History of diagnosed cardiovascular, neurological, or autonomic nervous system disease

Known arrhythmia or pacemaker use

Regular use of medications that may affect heart rate variability, such as beta blockers or antiarrhythmic drugs

Acute infection, fever, or any condition affecting general health status on the day of assessment

Trial design

Design model

Single group

Treatments tested in this trial

  • Heart Rate Variability and Blood Pressure Assessment

    Other intervention

    Participants will complete a single-visit resting physiological assessment under standardized conditions. After an adaptation period, systolic blood pressure, diastolic blood pressure, and pulse will be measured using an automated oscillometric upper-arm blood pressure monitor. Continuous RR interval data will then be recorded using the Polar H10 chest strap and analyzed with Kubios HRV software. Heart rate variability parameters will be calculated from predefined 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous recording for methodological comparison.

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Healthy Adult Assessment GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

RMSSD Across Different Analysis Durations

Root mean square of successive differences (RMSSD), in milliseconds (ms), calculated from predefined 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording obtained under standardized resting conditions.

Time frame
Baseline, during a single study visit
2

SDNN Across Different Analysis Durations

Standard deviation of normal-to-normal intervals (SDNN), in milliseconds (ms), calculated from predefined 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording obtained under standardized resting conditions.

Time frame
Baseline, during a single study visit
3

Low-Frequency Power Across Different Analysis Durations

Low-frequency (LF) power, in ms\^2, calculated from predefined 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording obtained under standardized resting conditions.

Time frame
Baseline, during a single study visit
4

High-Frequency Power Across Different Analysis Durations

High-frequency (HF) power, in ms\^2, calculated from predefined 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording obtained under standardized resting conditions.

Time frame
Baseline, during a single study visit.

Secondary outcomes

1

Agreement of RMSSD Across Different Analysis Durations

Agreement of RMSSD values, in milliseconds (ms), obtained from 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording, assessed using intraclass correlation coefficients and Bland-Altman analysis.

Time frame
Baseline, during a single study visit
2

Agreement of SDNN Across Different Analysis Durations

Agreement of SDNN values, in milliseconds (ms), obtained from 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording, assessed using intraclass correlation coefficients and Bland-Altman analysis.

Time frame
Baseline, during a single study visit
3

Agreement of Low-Frequency Power Across Different Analysis Durations

Agreement of low-frequency (LF) power values, in ms\^2, obtained from 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording, assessed using intraclass correlation coefficients and Bland-Altman analysis.

Time frame
Baseline, during a single study visit
4

Agreement of High-Frequency Power Across Different Analysis Durations

Agreement of high-frequency (HF) power values, in ms\^2, obtained from 1-minute, 5-minute, 10-minute, and 20-minute analysis windows extracted from the same continuous resting RR interval recording, assessed using intraclass correlation coefficients and Bland-Altman analysis.

Time frame
Baseline, during a single study visit

Other outcomes

Sponsors and contacts

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