Comparison of Heart Rate Variability Measurement on the Arm and Chest in Vagus Nerve Stimulation

Bahçeşehir University

Status: Enrolling

Conditions: Sympathetic; Imbalance

Treatments: Device: Transcutaneous Auricular Vagus Nerve Stimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT07000175

AVU10002

Details and patient eligibility

About

Healthy participants will be included in this study by invitation and randomised into three groups. Participants in each group will receive bilateral transcutaneous vagus nerve stimulation with the same frequency, current transit time and current intensity. Heart rate variability will be measured over the chest in the first group, over the right arm in the second group and over the left arm in the third group. Then, the differences between the groups in heart rate variability parameters (time-dependent, frequency-dependent) will be compared. The aim of this study is to examine the differences between heart rate variability measurements measured at different sites.

Full description

Heart rate variability is defined as the change in beat-to-beat interval, and the sympathetic and parasympathetic nervous system influences the change in beat-to-beat interval through cardiovascular connections. Heart rate variability measurement can be obtained by different methods. However, which method is more effective is controversial. The aim of this study was to investigate the differences between heart rate variability parameters measured on the chest, right arm and left arm.

Healthy participants aged 18-45 years will be included in the study. The inclusion criteria will be determined as being 18 years of age or older and not having any acute or chronic disease. Exclusion criteria will be determined as being previously involved in any neuromodulation intervention, smoking or alcohol use, and regular medication use.

Participants included in the study will be randomised into three groups and transcutaneous vagus nerve stimulation will be applied. The duration of treatment will be 20 minutes and single session stimulation will be performed. Current intensity, current passage time and frequency will be planned to be the same in each patient. Before and after stimulation, heart rate variability will be measured over the chest in the first group, over the right arm in the second group and over the left arm in the third group. Then, heart rate variability parameters (time-dependent, frequency-dependent) will be compared between the groups.

Enrollment: 39 estimated patients

Sex: All

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18 years of age or older
• To know how to read and write Turkish
• Not having any acute or chronic disease

Exclusion criteria

• Previous application of any neuromodulation method
• Smoking or alcohol use
• Use of any supplementary medication

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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39 participants in 3 patient groups

Measurement over the chest

Active Comparator group

Description:

Heart rate variability will be measured on the chest for 5 minutes before and after transcutaneous vagus nerve stimulation.

Treatment:

Device: Transcutaneous Auricular Vagus Nerve Stimulation

Measurement over the right arm

Active Comparator group

Description:

Heart rate variability will be measured on the right arm for 5 minutes before and after transcutaneous vagus nerve stimulation.

Treatment:

Device: Transcutaneous Auricular Vagus Nerve Stimulation

Measurement over the left arm

Active Comparator group

Description:

Heart rate variability will be measured on the left arm for 5 minutes before and after transcutaneous vagus nerve stimulation.

Treatment:

Device: Transcutaneous Auricular Vagus Nerve Stimulation