NCT07360821

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
3mo left

Started Feb 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress46%
Feb 2026Jul 2026

First Submitted

Initial submission to the registry

January 12, 2026

Completed
10 days until next milestone

First Posted

Study publicly available on registry

January 22, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

February 25, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Expected
Last Updated

January 22, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

January 12, 2026

Last Update Submit

January 17, 2026

Conditions

Keywords

SKNA; HRV; Blood Pressure Variability; Athletes; Cardiopulmonary Exercise Testing

Outcome Measures

Primary Outcomes (2)

  • Heart Rate Variability

    Time-domain metrics (e.g., RMSSD, SDNN) derived from ECG recordings to evaluate cardiovagal modulation and cardiac autonomic balance.

    Baseline (10-minute rest), during the 10-minute mental stress test, and during the cardiopulmonary exercise test (approx. 20 minutes)

  • Skin Sympathetic Nerve Activity

    Integrated average SKNA (aSKNA) and burst metrics measured via surface electrodes to assess sympathetic nerve firing

    Baseline (10-minute rest), during the 10-minute mental stress test, and during the cardiopulmonary exercise test (approx. 20 minutes)

Study Arms (4)

Sedentary Control

Healthy adults with minimal physical activity, screened via SBQ and IPAQ-S questionnaires as baseline controls

Diagnostic Test: Cardiopulmonary Exercise Testing

Endurance Athletes

Long-distance runners or triathletes with over 1 year of regular aerobic training (e.g., 800m+ running, swimming).

Diagnostic Test: Cardiopulmonary Exercise Testing

Strength Athletes

Athletes specializing in anaerobic/power-based training, such as weightlifting, wrestling, or sprinting.

Diagnostic Test: Cardiopulmonary Exercise Testing

Traditional Ethnic Sports

Practitioners of mind-body exercises like Tai Chi or Baduanjin, emphasizing respiratory control and mild intensity

Diagnostic Test: Cardiopulmonary Exercise Testing

Interventions

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

Endurance AthletesSedentary ControlStrength AthletesTraditional Ethnic Sports

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of 60-80 healthy adult volunteers (college students). Participants are categorized into five distinct groups based on their habitual physical activity levels and training backgrounds: 1) Sedentary controls, 2) Endurance athletes, 3) Strength athletes, 4) Technical athletes, and 5) Traditional ethnic sports practitioners (e.g., Tai Chi). Gender balance is maintained across all groups.

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Exercise Test

Intervention Hierarchy (Ancestors)

Heart Function TestsDiagnostic Techniques, CardiovascularDiagnostic Techniques and ProceduresDiagnosisRespiratory Function TestsDiagnostic Techniques, Respiratory SystemErgometryInvestigative Techniques

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 12, 2026

First Posted

January 22, 2026

Study Start

February 25, 2026

Primary Completion

April 30, 2026

Study Completion (Estimated)

July 30, 2026

Last Updated

January 22, 2026

Record last verified: 2026-01