- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07162584
- Original Trial
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
Intervention / Treatment
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
- Name: Keith M Kendrick, Dr
- Phone Number: 86-28-61830811
- Email: k.kendrick.uestc@gmail.com
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- UESTC-neuSCAN-87
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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