Heart Rate Variability, Biomarker of Stress

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Review clinical trials related to Heart Rate Variability, Biomarker of Stress. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Virtual vs. Traditional CPR Training: Effects on Stress

This medical education study investigates stress levels among undergraduate medical students during basic life support (BLS) training. It compares traditional face-to-face teaching session with virtual reality (VR) training simulating a resuscitation scenario in a public place. We will measure heart rate, heart rate variability, and self-reported stress to assess acute stress responses. The study also examines physical sensations related to VR, the realism of the virtual environment, and the suitability of VR for BLS training.

Participants needed: 60
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Oulu University HospitalUpdated: Aug 29, 2025Locations: 1
Eligibility criteria

Volunteers (18-30 years old) will be recruited from first- and second-year medic... [+1]

Pregnant individuals will not be included [+2]

Status: Not yet recruiting

Stress Evaluation and Management Using High Fidelity Simulation in Medical Education

The goal of this interventional study is to collect clinical and neurophysiological information to determine whether high-fidelity simulation can serve as a stress-inducing stimulus in a population of healthy residents (Emergency medicine, Anesthesia and Intensive care medicine, Paediatrics), both male and female, aged between 25 and 40 years. The main questions it aims to answer are: 1. Define in which phase of the simulation the highest level of stress is observed. 2. Determine the level of stress reached after performing a second high-fidelity simulation after a period of time. 3. Identify whether specific brain areas are activated during high-fidelity simulation. Participants will form teams, consisting of three medical trainees from the same specialty training program, that will undergo two high-fidelity simulations based on a clinical scenario relevant to their residency. * During the simulation, automatic pupillometry will be performed on all team members at the four time points. * Additionally, a two-lead ECG will be recorded for all team members at baseline and end of the debriefing * One team member will undergo EEG monitoring throughout the entire simulation. The EEG recordings will be sampled at baseline, during the simulation and end of the debriefing.

Participants needed: 45
Trial details
Age: 25-40Biological sex: AllType: InterventionalSponsor: Fondazione Policlinico Universitario Agostino Gemelli IRCCSUpdated: Apr 8, 2025
Eligibility criteria

Medical trainees from the specialties of Emergency Medicine, Anesthesia and Inte... [+1]

Known history of psychiatric disorders, cognitive impairment, or cardiac arrhyth... [+3]