The Effect and Mechanism of taVNS in Modulating Human Social Attention

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorUniversity of Electronic Science and Technology of China

About this trial

The objectives of this study are to investigate:

1. whether non-invasive transcutaneous auricular vagus nerve stimulation (taVNS) can enhance human interest in social stimuli in free-viewing and stressful tasks; 2. whether its effect on brain function occurs via modulating endogenous oxytocin release; 3. how the stimulation site and various parameters of taVNS should be set to effectively promote the above-mentioned changes in brain function.

The main questions it aims to answer are:

1. Does taVNS facilitate a preference for social relative to non-social stimuli in both free-viewing and stressful tasks? 2. Does taVNS increase peripheral concentrations of the neuropeptide oxytocin, and whether these changes are associated with enhanced social attention? 3. Does taVNS stimulation of the right tragus, left tragus, or bilateral tragus sites produce the strongest effects on oxytocin release and social attention?

Investigators will compare the effects of taVNS targeting the left tragus, right tragus, or bilateral tragus with ear-lobe sham stimulation (no vagal activation). Eye-tracking will be used across multiple experimental paradigns. For measurements of oxytocin (OT) and arginine vasopressin (AVP), saliva samples will be collected at baseline, immediately after taVNS, 20 min post-stimulation, and 30 min post-stimulation. Investigators will test whether (a) taVNS facilitates social attention, and (b) its effects are associated with elevated OT and AVP release.

Investigators hypothesize that taVNS will enhance social attention and oxytocin release, that changes in social attention will be associated with the magnitude of oxytocin release, and that bilateral tragus stimulation will produce the strongest effects on both social attention and oxytocin release.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

History of past or current neurological/psychiatric disorders;

Use of psychotropic medications (including nicotine and alcohol)

Visual impairments

Baseline data exceeds ±3 SD from mean

Trial design

Design model

Parallel

Treatments tested in this trial

  • taVNS

    Device

    bilateral Transcutaneous Auricular Vagus Nerve Stimulation on earlobe

  • taVNS

    Device

    Transcutaneous Auricular Vagus Nerve Stimulation on left tragus

  • taVNS

    Device

    taVNS only on the right tragus

  • taVNS

    Device

    taVNS on the bilateral tragus

Treatment groups

120 Participants
are divided into 4 treatment groups
Group A: Experimental: earlobe stimulationPlacebo comparator 1 intervention
Group B: left tragus stimulationExperimental treatment 1 intervention
Group C: right tragus stimulationExperimental treatment 1 intervention
Group D: bilateral tragus stimulationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Fixation time on different areas of interest (AOIs) in free viewing tasks

The total time spent viewing specific AOIs in free viewing tasks will be recorded

Time frame
baseline: one week before the stimulation; post: immediately after the 30 min sham (earlobe) or taVNS (transaural vagal stimulation) stimulation.
2

Fixation counts on different AOIs in free viewing tasks

The number of fixations on specific AOIs during presentation of visual stimuli will be recorded

Time frame
baseline: one week before the stimulation; post: immediately after the 30 min of sham or taVNS stimulation
3

Errors made in the stressful antisaccade task

The number of errors in the direction opposite to the required direction

Time frame
baseline: one week before the stimulation; post: immediately after the 30 min of sham or taVNS stimulation
4

Response time in the stressful antisaccade task

Time taken to make the first saccade towards the required direction

Time frame
baseline: one week before the stimulation; post: immediately after the 30 min sham or taVNS stimulation

Secondary outcomes

1

Saliva oxytocin concentrations

Four saliva samples will be collected at different time points during the experiment and oxytocin concentrations measured by assay

Time frame
T1: baseline; T2: immediately after the 30 min sham or taVNS stimulation; T3: 20 mins after the stimulation; T4: 30 mins after the stimulation.
2

Saliva vasopressin concentrations

Four saliva samples will be collected at different time points during the experiment and vasopressin concentrations measured by assay

Time frame
T1: baseline; T2: immediately after the 30 min sham or taVNS stimulation; T3: 20 mins after the stimulation; T4: 30 mins after the stimulation.
3

State anxiety scores

Subjects will complete the State Anxiety Questionnaire before and after stimulation

Time frame
baseline: before the stimulation post: immediately after the 30 min sham or taVNS stimulation
4

Positive and negative affective schedule (PANAS) scores

Subjects will complete the PANAS questionnaire before and after stimulation

Time frame
baseline: before the stimulation; post: immediately after the 30 min sham or taVNS stimulation.

Other outcomes

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