- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07815496
The Effects of Oxytocin on Fairness Perception and Related Prosocial Behaviors
The Modulatory Effects of Oxytocin on Fairness Perception and Related Prosocial Behaviors
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Shuxia Yao, Dr
- Phone Number: 86+18111297596
- Email: yaoshuxia@uestc.edu.cn
Study Locations
-
-
Sichuan
-
Chengdu, Sichuan, China, 611731
- Recruiting
- University of Electronic Science and Technology of China (UESTC)
-
Contact:
- Shuxia Yao, Dr
- Phone Number: 86+18111297596
- Email: yaoshuxia@uestc.edu.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Investigators
- Principal Investigator: Shuxia Yao, Dr, University of Electronic Science and Technology of China
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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