ClinicalTrials.gg
RecruitingNCT07798349Updated Sep 1, 2026

The Effect and Mechanism of taVNS in Modulating Human Social Attention

An interventional study of taVNS and taVNS in Healthy Adult, Role of Vagal Stimulation in Oxytocin Release and Role of Vagal Stimulation in Social Attention, sponsored by University of Electronic Science and Technology of China. Recruiting at 1 site in China. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by University of Electronic Science and Technology of China · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Started Aug 2026; still recruiting 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

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.

Read the detailed description

In a placebo-controlled, single-blind, mixed-design experiment, investigators plan to determine whether taVNS modulates human social attention and whether such effects depend on oxytocin (OT) modulation.

Participants will first complete free-viewing and stressful tasks to establish baseline social attention. Consistent with prior studies, participants whose baseline data exceed ±3 SD will be excluded from the study. One week later, eligible participants will complete the Chinese-language versions of several questionnaires prior to intervention: the Behavioral Activation System Scale (BAS), Behavioral Inhibition System Scale (BIS), Trait Anxiety Inventory, State Anxiety Inventory (STAI), Liebowitz Social Anxiety Scale (LSAS), Beck Depression Inventory (BDI), Autism Spectrum Quotient (AQ), Positive and Negative Affect Schedule (PANAS), and Interpersonal Reactivity Index (IRI).

Next, the first saliva sample (T1: 1-2 mL, passive drool) will be collected, followed by 30-min non-invasive taVNS (left, right, or bilateral tragus) or sham (earlobe) intervention. A second saliva sample (T2) will be obtained immediately post-stimulation. Behavioral assessments - including free-viewing paradigms of social and non-social stimuli and a stressful antisaccade paradigm - will begin after T2 collection. Social-attention metrics (response time, errors, fixation duration, fixation counts, etc.) will be recorded using eye-tracking equipment.

Upon completion of the eye-tracking tasks, the third saliva sample (T3: \~20 min post-stimulation) will be collected. Participants will then repeat the State Anxiety and PANAS (mood) questionnaires to evaluate intervention-related changes in anxiety and mood. A fourth saliva sample (T4: \~30 min post-stimulation) will subsequently be obtained.

A mixed-linear model or mixed-model ANOVA, followed by appropriate post-hoc analyses, will be applied to eye-tracking behavioural data and questionnaires scores to evaluate intervention effects.

Investigators hypothesize that taVNS will increase social attention and oxytocin release, that social attention changes will be associated with the magnitude of oxytocin release and that bilateral tragus stimulation will be the most effective

02

Conditions studied

  • Healthy Adult
  • Role of Vagal Stimulation in Oxytocin Release
  • Role of Vagal Stimulation in Social Attention

Keywords

  • taVNS
  • social attention
03

In context

Lead sponsor

University of Electronic Science and Technology of China is the lead sponsor of 112 studies on the registry; 37 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Healthy adults

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
120 participants (estimated)

Study arms

  • Placebo comparator
    Experimental: earlobe stimulation

    Subjects will receive bilateral ear lobe stimulation as a control for taVNS

    Device: taVNS

  • Experimental
    left tragus stimulation

    Subjects will receive the taVNS only on the left tragus

    Device: taVNS

  • Experimental
    right tragus stimulation

    Subjects will receive the right tragus stimuliation

    Device: taVNS

  • Experimental
    bilateral tragus stimulation

    Subjects will receive bilateral tragus stimulation

    Device: taVNS

Interventions

  • DevicetaVNS

    bilateral Transcutaneous Auricular Vagus Nerve Stimulation on earlobe

  • DevicetaVNS

    Transcutaneous Auricular Vagus Nerve Stimulation on left tragus

    Also known as: Transcutaneous Auricular Vagus Nerve Stimulation

  • DevicetaVNS

    taVNS only on the right tragus

  • DevicetaVNS

    taVNS on the bilateral tragus

06

What researchers measure

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.

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07798349
Responsible party
Sponsor
First posted
Sep 1, 2026
Start date
Aug 1, 2026
Primary completion
Nov 30, 2026 (estimated)
Completion
Nov 30, 2026 (estimated)
Last update
Sep 1, 2026

Study contacts

Keith M Kendrick PhD
Contact
k.kendrick.uestc@gmail.com
86-28-61830811
yan zhang
Contact
532769737@qq.com
18215678419

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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