The Effects of Oxytocin on Fairness Perception and Related Prosocial Behaviors

September 8, 2026 updated by: Shuxia Yao, University of Electronic Science and Technology of China

The Modulatory Effects of Oxytocin on Fairness Perception and Related Prosocial Behaviors

This study aims to investigate the modulation of intranasally administered oxytocin (24 IU) on human fairness perception and related prosocial behaviors.

Study Overview

Status

Recruiting

Detailed Description

Fairness preference is a cornerstone of human sociality, often driving individuals to incur personal costs in order to uphold fairness norms. Oxytocin (OT), a neuropeptide, is considered a potential modulator of prosocial behavior, yet its specific mechanism of action in fairness decision-making remains unclear. Previous research has predominantly focused on the overall effects of OT on behaviors, without differentiating its roles across distinct processing stages such as cognitive evaluation and emotional anticipation. Furthermore, there is a lack of systematic investigation into whether its effects are modulated by social context and gain-loss contexts. Using a randomized, double-blind, placebo-controlled between-subjects design, the present study combines functional magnetic resonance imaging (fMRI) with the Dictator Game (DG) and the Ultimatum Game (UG) to elucidate how intranasal OT influences fairness perception and related prosocial behavior. The UG additionally involves strategic considerations of the proposer arising from the recipient's ability to reject the offer. Participants, act as proposers, are instructed to rate their perceived levels of fairness and guilt when receiving advantageous inequity and fair allocations in both gain and loss contexts. Following ratings, participants make decisions of accepting or rejecting the current allocation. Their brain activity and behavioral responses will be synchronously recorded during the tasks, and scores of questionnaires including Positive and Negative Affect Schedule, State-Trait Anxiety Inventory, Sensitivity to Punishment and Sensitivity to Reward Questionnaire, Social Value Orientation, Self-Report Altruism Scale, Prosocial Tendencies Measure, Behavioral Inhibition System and Behavioral Activation System Scale, Interpersonal Reactivity Index, Toronto Alexithymia Scale, Beck Depression Inventory-Ⅱ, Guilt and Shame Proneness Scale, Test of Self-Conscious Affect 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 (UESTC)
        • Contact:

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 (24IU)
Placebo Comparator: placebo group
male and female subjects with placebo treatment
intranasal administration of placebo (24IU)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fairness rating scores
Time Frame: 1 hour
Participants are asked to rate their perceived levels of fairness on a 9-point Likert scale (1 = highly fair, 9 = highly unfair) to the computer's allocation in each trial.
1 hour
Anticipated guilt rating scores
Time Frame: 1 hour
Participants are asked to rate the anticipated guilt they would feel if they accepted the allocation given by the computer in each trial. Ratings were conducted on a 9-point Likert scale (1 = not at all, 9 = highly guilty).
1 hour
The binary decision to the initial allocation
Time Frame: 1 hour
Participants are asked to makde decisions of accepting or rejecting the allocation provided by the computer in each trial.
1 hour
Brain activity patterns
Time Frame: 1 hour
Brain activity patterns in response to the outcome of the allocation given by computer and the binary decision. We will examine these brain response patterns via both the conventional univariate analysis and the machine learning-based multivariate pattern analysis (MVPA) approaches.
1 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Inequity aversion parameters derived from the Fehr-Schmidt model
Time Frame: 1 hour

Inequity aversion parameters derived from the Fehr-Schmidt model are used to elucidate whether OT would modulate inequity aversion. This model-based analysis was conducted based on choices using hierarchical Bayesian modeling. In the Fehr-Schmidt model, the subjective value of a given allocationis determined by one's own and the other's allocation using the following formula:

SV(Mself, Mother) = Mself - βmax{ Mself - Mother, 0}, Mself ≠ Mother where Mself is one's payoff and Mother is the other's payoff. Parameter β represents the weight assigned to inequity. Higher parameter values indicate a stronger degree of inequity aversion in participants.

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 5, 2026

Primary Completion (Estimated)

December 30, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

September 3, 2026

First Submitted That Met QC Criteria

September 8, 2026

First Posted (Actual)

September 11, 2026

Study Record Updates

Last Update Posted (Actual)

September 11, 2026

Last Update Submitted That Met QC Criteria

September 8, 2026

Last Verified

September 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UESTC-neuSCAN-105

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

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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