About this trial
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.
Eligibility criteria
Qualifiers
18 years of age or older
To know how to read and write Turkish
Not having any acute or chronic disease
Disqualifiers
Previous application of any neuromodulation method
Smoking or alcohol use
Use of any supplementary medication
Trial design
Treatments tested in this trial
- Transcutaneous Auricular Vagus Nerve Stimulation