Oxytocin and Human Defensive Responses in a Dynamic Situation

September 30, 2025 updated by: Shuxia Yao, University of Electronic Science and Technology of China

The Modulatory Affect of Oxytocin on Human Defensive Responses During Dynamic Predator-prey Interactions

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.

Study Overview

Status

Recruiting

Conditions

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.

Study Type

Interventional

Enrollment (Estimated)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Sichuan
      • Chengdu, Sichuan, China, 611731
        • Recruiting
        • University of Electronic Science and Technology of China

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy subjects without past or current psychiatric or neurological disorders

Exclusion Criteria:

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: oxytocin group
male and female subjects with oxytocin treatment
intranasal administration of oxytocin (24 IU)
Placebo Comparator: placebo group
male and female subjects with placebo treatment
intranasal administration of placebo (24 IU)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Escape sucess rates when confronting different predators
Time Frame: 1 hour
Escape sucess rates in successfully entering the refuge when confronting the fast, medium and slow predators.
1 hour
Flight initiation distance
Time Frame: 1 hour
It is the prey-predator distance when a prey flees from a threat, a key index quantifying escape decisions.
1 hour
The distance to refuge
Time Frame: 1 hour
The distance to refuge when a prey flees from a threat.
1 hour
Brain activity patterns in response to threats along the predatory imminence continuum
Time Frame: 1 hour
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).
1 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Confidence rating scores
Time Frame: 1 hour
Participants are asked to rate their confidence levels in successfully escaping from the predator before each block.
1 hour
Anxiety rating scores
Time Frame: 1 hour
Particioants are asked to rate how anxious they felt during the escape decision-making process.
1 hour
SCR during task
Time Frame: 1 hour
Skin Conductance Response (SCR) data are recorded in the task during scanning.
1 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Shuxia Yao, Dr, University of Electronic Science and Technology of China

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 13, 2025

Primary Completion (Estimated)

January 15, 2026

Study Completion (Estimated)

January 28, 2026

Study Registration Dates

First Submitted

September 1, 2025

First Submitted That Met QC Criteria

September 1, 2025

First Posted (Estimated)

September 9, 2025

Study Record Updates

Last Update Posted (Estimated)

October 6, 2025

Last Update Submitted That Met QC Criteria

September 30, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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