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RecruitingNCT07162584Updated Oct 6, 2025

Oxytocin and Human Defensive Responses in a Dynamic Situation

An interventional study of Oxytocin nasal spray and Placebo in Healthy, sponsored by University of Electronic Science and Technology of China. Recruiting at 1 site in China. Open to participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-10-06.

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

From the registry’s dates

  • Primary completion was expected by Jan 2026, 8 months ago, but the record still lists the study as recruiting.
  • Started Sep 2025; still recruiting 1 year later.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

The presnet study is to investigate the effect of intranasal oxytocin (24 IU) treatment on modulating how human responsd to threat in a dynamic situation.

Read the detailed description

Predator-prey interactions are inherently dynamic, requiring adaptive responses from prey to survive. Altough there is eviedence for oxytocin modulating anxiety and fear responses to threats, it remains unclear whether oxytocin (OT) would modulate how humans respond to threats along the predatory imminence continuum to facilitate escape during such interactions. Our study therefore focuses on this question by combining behavioralmeasures, skin conductance response, and fMRI in a dynamic predator-prey interaction paradigm. In this double-blind, between-subject, placebo-controlled study, participants are instructed to escape by evaluating the relative distance between themselves (i.e., the prey), the predator (slow, medium and high attacking speed) and the refuge. The MRI and Biopac electrophysiological acquisition systems are used in the study to collect subjects' brain activity and skin conductance response. Participants are also asked to rate their confidence and anxiety levels during performing the task. We will aslo examine the resulted patterns of flight initiation distance (FID) and distance to refuge (DTR) when the prey fled from different predators. Scores of questionnaires including Positive and Negative Affect Schedule, State-Trait Anxiety Inventory, Beck Depression Inventory-Ⅱ, Autism Spectrum Quotient, Sensitivity to Punishment and Sensitivity to Reward Questionnaire, General Risk Propensity Scale are also collected before the experiment.

02

Conditions studied

  • Healthy

Keywords

  • oxytocin
  • fMRI
  • escape decisions
  • dynamic predator-prey interaction
  • defensive responses
03

In context

Lead sponsor

University of Electronic Science and Technology of China is the lead sponsor of 109 studies on the registry; 35 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Healthy subjects without past or current psychiatric or neurological disorders

Exclusion criteria

Exclusion Criteria:

  • History of head injury; pregnant, menstruating, taking oral contraceptives; medical or psychiatric illness,
  • The presence of metal in the body or claustrophobia.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    oxytocin group

    male and female subjects with oxytocin treatment

    Drug: Oxytocin nasal spray

  • Placebo comparator
    placebo group

    male and female subjects with placebo treatment

    Drug: Placebo

Interventions

  • DrugOxytocin nasal spray

    intranasal administration of oxytocin (24 IU)

  • DrugPlacebo

    intranasal administration of placebo (24 IU)

06

What researchers measure

Primary outcomes

  1. Escape sucess rates when confronting different predators

    Escape sucess rates in successfully entering the refuge when confronting the fast, medium and slow predators.

    Time frame: 1 hour

  2. Flight initiation distance

    It is the prey-predator distance when a prey flees from a threat, a key index quantifying escape decisions.

    Time frame: 1 hour

  3. The distance to refuge

    The distance to refuge when a prey flees from a threat.

    Time frame: 1 hour

  4. Brain activity patterns in response to threats along the predatory imminence continuum

    Brain activity patterns in response to different predators along the predatory imminence continuum. We will examine these brain response patterns via both the conventional univariate analysis and the machine learning-based multivariate pattern analysis (MVPA) approaches. Based on previous studies, the medium predator is a priori used as an anchor for fast and slow predators for a more sensitive measure of brain activity differences and contrasts with the medium predator would be reported in the suplemental files for completeness (if there were significant effects).

    Time frame: 1 hour

Secondary outcomes

  1. Confidence rating scores

    Participants are asked to rate their confidence levels in successfully escaping from the predator before each block.

    Time frame: 1 hour

  2. Anxiety rating scores

    Particioants are asked to rate how anxious they felt during the escape decision-making process.

    Time frame: 1 hour

  3. SCR during task

    Skin Conductance Response (SCR) data are recorded in the task during scanning.

    Time frame: 1 hour

07

Study locations

1 of 1 sites recruiting
  • University of Electronic Science and Technology of China
    Chengdu, Sichuan 611731, China
    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 Oct 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07162584
Lead sponsor
University of Electronic Science and Technology of China
Responsible party
Shuxia Yao (Associate Professor, University of Electronic Science and Technology of China) — Principal investigator
First posted
Sep 9, 2025
Start date
Sep 13, 2025
Primary completion
Jan 15, 2026 (estimated)
Completion
Jan 28, 2026 (estimated)
Last update
Oct 6, 2025

Study contacts

Keith M Kendrick, Dr
Contact
k.kendrick.uestc@gmail.com
86-28-61830811
Shuxia Yao, Dr
principal investigator · University of Electronic Science and Technology of China

Oversight

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

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