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Clinical Trials in Italy / NCT07781670
Recruiting Not applicable

Neurophysiological and Autonomic Responses to Acute Physical and Emotional Stress: An EEG Study

NCT07781670 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2026-08-01
Last updated
2026-08-24

Condition(s) studied

StressAcute Stress

Investigational drug(s) / intervention(s)

Cold Pressor TestNegative Autobiographical Memory RecallAffective Picture-Viewing Task

Cold Pressor Test: Participants will immerse one hand in an ice-water bath and will be instructed to maintain the immersion for as long as tolerable, up to a maximum of three minutes. Participants may withdraw their hand at any time if the stimulation becomes intolerable. The actual duration of hand immersion will be recorded as an index of pain tolerance. EEG and autonomic activity will be continuously recorded during the task.

Negative Autobiographical Memory Recall: Participants will be instructed to select a personally painful or distressing autobiographical memory and focus on its emotional and experiential aspects for three minutes while seated with their eyes closed. No specific autobiographical event will be suggested by the researcher. EEG and autonomic activity will be continuously recorded during the task.

Affective Picture-Viewing Task: Participants will view negative and neutral images selected from the Nencki Affective Picture System (NAPS). Each trial will consist of a 10-second fixation period followed by a 30-second image presentation. Images will be presented in randomized order while EEG and autonomic activity are continuously recorded.

Study summary

This study aims to investigate neurophysiological, autonomic, and subjective responses to different acute physical and emotional stress-inducing conditions using a within-subject repeated-measures design.

Participants will complete four experimental conditions: a resting-state baseline, a Cold Pressor Test, a negative autobiographical memory recall task, and an affective picture-viewing task using stimuli selected from the Nencki Affective Picture System (NAPS). The order of the experimental stress conditions will be randomized or counterbalanced to minimize potential order and carry-over effects.

Electroencephalographic (EEG) and autonomic activity will be recorded throughout the experimental session. Autonomic measures will include heart rate (HR), heart rate variability (HRV), electrodermal activity (EDA), and skin conductance responses (SCR). Subjective levels of stress, anxiety, and pain will be assessed using visual analogue scales (VAS).

Participants will also complete validated psychological measures assessing resilience, perceived stress, and state and trait anxiety, together with the Tower of London task as a behavioral measure of executive planning.

The primary objective is to characterize the modulation of EEG alpha-band activity during acute physical stress, with the main comparison focusing on the Cold Pressor Test relative to resting-state baseline. Secondary and exploratory objectives include comparing cortical, autonomic, and subjective responses across experimental conditions and investigating whether individual psychological characteristics and executive functioning are associated with differences in psychophysiological stress responses.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Age between 18 and 65 years. * Ability to understand the study procedures and provide written informed consent. * Sufficient knowledge of the Italian language to understand study instructions and complete the psychological assessments. Exclusion Criteria: * History of major neurological disorders or other medical conditions that could significantly affect EEG or autonomic measurements. * Current severe psychiatric disorder that could interfere with participation in the experimental procedures. * Cardiovascular conditions for which exposure to the Cold Pressor Test may be contraindicated. * Medical conditions affecting peripheral circulation or sensitivity of the upper limbs that could interfere with or increase the risk associated with the Cold Pressor Test. * Current use of medications that may substantially affect autonomic or central nervous system activity, when considered clinically relevant to the study procedures. * Presence of wounds, injuries, or other conditions affecting the hand that would prevent safe completion of the Cold Pressor Test. * Inability to complete the experimental procedures or provide valid informed consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Pavia Pavia Lombardy Recruiting

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07781670 on ClinicalTrials.gov ↗ ← All trials in Italy