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Not yet recruiting NCT07360821

Investigation of Autonomic Stress Response Patterns in College Students With Varying Physical Activity Levels

Observational Autonomic Nervous System Activity Cardiovascular Physical Activity Level

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cardiopulmonary Exercise Testing.
Who it may be relevant to
Registry conditions: Autonomic Nervous System Activity, Cardiovascular, Physical Activity Level. Basic parameters: 18 years — 30 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study aims to investigate the differences in cardiovascular stress response patterns among individuals with various physical activity levels (sedentary controls and different types of athletes). By synchronously monitoring ECG, heart rate, skin sympathetic nerve activity (SKNA), blood pressure, and cardiac output, the study will characterize physiological dynamics during resting, orthostatic challenge, cold pressor stress, and maximal exercise.

Detailed description

Participants will be categorized into five groups based on their training background: sedentary, endurance, strength, technical, and traditional ethnic sports. The experimental protocol includes baseline measurements in lying, standing, and sitting positions, followed by a series of acute stress tests: a lie-to-stand orthostatic test, a slow breathing test, and a cold pressor test. Finally, participants will perform a ramp incremental exercise test on a cycle ergometer. Synchronous physiological data including HRV and SKNA will be collected to evaluate the dynamic regulation of the autonomic nervous system.

Interventions

  • Diagnostic test Cardiopulmonary Exercise Testing
    Cardiopulmonary Exercise Testing (CPET) is a non-invasive, integrated assessment of the cardiovascular, respiratory, and muscular systems' responses to physical stress.

Primary outcome measures

  • Heart Rate Variability [Time frame: Baseline (10-minute rest), during the 10-minute mental stress test, and during the cardiopulmonary exercise test (approx. 20 minutes)]
  • Skin Sympathetic Nerve Activity [Time frame: Baseline (10-minute rest), during the 10-minute mental stress test, and during the cardiopulmonary exercise test (approx. 20 minutes)]

Eligibility criteria

Inclusion criteria

Healthy young adults aged 18-25 years

Body Mass Index (BMI) within the range of 18.5-23.9 kg/m 2

No history of systematic professional athletic training (for sedentary group) or confirmed training background (for athlete groups)

No exercise contraindications or history of cardiovascular, respiratory, or metabolic diseases

No family history of sudden cardiac death

Ability to understand the study protocol and sign the informed consent form

Exclusion criteria

History of limb sports injury within the past 6 months or unhealed fractures

Habits of smoking or chronic alcohol consumption

Presence of implanted electronic devices (e.g., pacemakers)

Clinical diagnosis of psychiatric disorders such as anxiety or depression

Recent use of medications affecting autonomic or cardiovascular function

Regular practice of meditation or ongoing psychotherapy

Irregular menstrual cycles (for female participants)

Peripheral neuropathy or other autonomic nervous system disorders

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07360821 · 2025601H · 2025601H

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗