ClinicalTrials.gg
RecruitingNCT07815496Updated Sep 11, 2026

The Effects of Oxytocin on Fairness Perception and Related Prosocial Behaviors

An interventional study of Oxytocin nasal spray and Placebo in Healthy Adult Participants, 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 2026-09-11.

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

From the registry’s dates

  • Started Sep 2026; still recruiting 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

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

Read the 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.

02

Conditions studied

  • Healthy Adult Participants

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Keywords

  • oxytocin
  • fMRI
  • fairness perception
  • prosocial behavior
03

In context

Altruism

29 studies on the registry are indexed under Altruism; 7 are open to participants now.

This study's planned enrollment of 80 is below the median of 241 across 27 interventional studies indexed under Altruism.

Browse Altruism studies →

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 35 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 subjects without past or current psychiatric or neurological disorders.

Exclusion criteria

Exclusion Criteria:

  • History of head injury; pregnant, menstruating, taking oral ; medical or psychiatric illness.
  • The presence of metal in the body or claustrophobia.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

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

  • intranasal administration of oxytocin (24IU)

  • DrugPlacebo

    intranasal administration of placebo (24IU)

06

What researchers measure

Primary outcomes

  1. Fairness rating scores

    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.

    Time frame: 1 hour

  2. Anticipated guilt rating scores

    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).

    Time frame: 1 hour

  3. The binary decision to the initial allocation

    Participants are asked to makde decisions of accepting or rejecting the allocation provided by the computer in each trial.

    Time frame: 1 hour

  4. Brain activity patterns

    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.

    Time frame: 1 hour

Secondary outcomes

  1. Inequity aversion parameters derived from the Fehr-Schmidt model

    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.

    Time frame: 1 hour

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

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Sep 2026 (actual). Primary completion is estimated for Dec 2026, 3 months after the start.

Of 20 interventional studies with no phase under Altruism, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 8 and three quarters within 15. This study's planned 3 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 3, 2026
First posted
Sep 11, 2026
StartActual
Sep 5, 2026
Primary completionEst.
Dec 30, 2026
CompletionEst.
Dec 31, 2026
Last update
Sep 11, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07815496
Responsible party
Shuxia Yao (Associate Professor, University of Electronic Science and Technology of China) — Principal investigator
First posted
Sep 11, 2026
Start date
Sep 5, 2026
Primary completion
Dec 30, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Sep 11, 2026

Study contacts

Shuxia Yao, Dr
Contact
yaoshuxia@uestc.edu.cn
86+18111297596
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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Studies of the drug tested here: Oxytocin

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