This study examines how individuals respond to performance-related tasks and whether a non-invasive ear stimulation device influences stress responses during those tasks. Participants will be randomly assigned to use either an active or inactive (placebo) version of a transcutaneous vagus nerve stimulation (tVNS) device during a laboratory session.

The study includes two task conditions. In one condition, participants will prepare a brief speech under evaluative conditions designed to induce stress. In the other condition, participants will complete a non-evaluative writing task. During the session, participants will wear a heart rate monitor and complete short questionnaires assessing their current feelings, including state anxiety.

The primary objective is to determine whether active tVNS is associated with lower state anxiety during a performance-related stress task compared to placebo stimulation. Secondary outcomes include heart rate and task-related responses. The study will also examine whether individual differences in stress reactivity influence responses to stimulation.

Participation involves one laboratory session lasting approximately 45 minutes.

This study is a laboratory-based, randomized, double-blind experiment designed to examine whether non-invasive transcutaneous vagus nerve stimulation (tVNS) influences state anxiety and physiological arousal during performance-related stress.

Participants will be randomly assigned to one of four conditions in a 2 × 2 between-subjects factorial design:

Device Condition:

Active tVNS

Placebo (inactive) tVNS

Task Condition:

Stress Task (Modified Trier Social Stress Test speech preparation)

Control Task (Non-evaluative writing task)

The device condition is double blind. Half of the devices are configured by the manufacturer to deliver active stimulation to the auricular branch of the vagus nerve via the left ear. The remaining devices are configured to deliver brief initial stimulation that ramps down to zero (placebo condition). Neither participants nor experimenters are aware of device assignment during the session.

After informed consent and baseline measures, participants complete a quiet baseline period during which heart rate and state anxiety are assessed. Participants then wear the tVNS device during structured laboratory tasks.

In the stress condition, participants are instructed to prepare a five-minute speech to be delivered before evaluators and recorded for assessment. The preparation phase is modeled after the Trier Social Stress Test and is designed to induce anticipatory evaluative stress. The speech is not ultimately delivered. State anxiety and heart rate are measured during preparation and immediately afterward.

In the control condition, participants complete a non-evaluative writing task on the same topic without evaluative framing. Physiological and self-report measures are collected at matched time points.

The primary outcome measure is state anxiety assessed using the short-form State-Trait Anxiety Inventory (STAI). Secondary outcomes include heart rate measured during baseline, task preparation, and recovery periods. Additional measures include dispositional stress reactivity, which will be examined as a potential moderator of stimulation effects.

The study is designed to determine whether active tVNS reduces subjective anxiety and physiological arousal during evaluative stress compared to placebo stimulation and to assess whether effects differ as a function of individual differences in stress reactivity.

Participation consists of a single laboratory session lasting approximately 45 minutes.

Inclusion Criteria:

- Adults aged 18 to 65 years

Fluent in English

Able to provide informed consent

Able to complete study procedures during a single laboratory session

Exclusion Criteria:

- History of neurological or psychiatric disorders

Cardiovascular disease or uncontrolled hypertension

Implanted electrical devices (e.g., pacemaker)

Current pregnancy

Contraindications to transcutaneous vagus nerve stimulation (tVNS)

Current use of medications that significantly affect autonomic nervous system functioning

Individual participant data will not be shared due to confidentiality considerations and institutional data protection policies. Although research data will be de-identified and stored securely, there are no current plans to make individual-level data publicly available. Aggregate results may be reported in publications and presentations.

Participants are blinded to device condition (active vs sham stimulation). Study personnel interacting with participants and collecting outcome data are blinded to condition assignment. Devices are pre-programmed and coded to maintain masking throughout the study.