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Oxytocin Modulates Eye Gaze Behavior During Social Processing

Oxytocin Modulates Eye Gaze Behavior During Social Processing and Associations With Trait Autism

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03293511
Enrollment
40
Registered
2017-09-26
Start date
2017-06-09
Completion date
2019-07-31
Last updated
2018-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Oxytocin, Eye tracking, Autistic trait

Brief summary

The main aim of the study is to examine whether the effects of intranasal oxytocin on eye-gaze behavior towards social stimuli are modulated via individual differences in trait autism

Detailed description

In this double-blind, within subject, placebo controlled design a total of n = 40 healthy male subjects will receive either 24 IU of oxytocin or placebo (interval between administration \> two weeks). 45 minutes after treatment subjects will undergo a total of 7 eye-tracking paradigms examining eye-gaze behavior during social processing: (1) dynamic social-nonsocial visual preference task during which movies of dynamic geometric images (DGI) and dynamic social images (DSI) will be presented; (2) non-biological versus biological motion task; (3) social attention and motivation of sharing enjoyment; (4) preference for emotional faces versus schematic faces (emoticons); (5) shared social attention - shared gaze direction with an actor shifting his attention to different objects; (6) preferred visual scanning of face regions in emotional faces; and, (7) eye gaze in response to empathy eliciting visual stimuli. Autistic and associated traits will be assessed using the Autism Spectrum Quotient (ASQ), Social Responsibilities Scale (SRS) and the Interpersonal Reactivity Index (IRI). Within-subject differences in the effects of oxytocin on social eye gazing behaviour will be related to individual differences in autistic traits.

Interventions

DRUGintranasal oxytocin

24 IU of oxytocin nasal spray will be applied to each subject.

DRUGintranasal placebo

24 IU of of placebo nasal spray will be applied to each subject.

Sponsors

University of Electronic Science and Technology of China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Intervention model description

Randomized placebo-controlled double-blind within-subject design

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy subjects without any past or present psychiatric or neurological disorders

Exclusion criteria

* History of brain injury * Visual impairments * Use of medication * Contraindications for oxytocin administration

Design outcomes

Primary

MeasureTime frameDescription
Global eye gaze characteristic: differences between oxytocin and placebo treatment45-90 minutes after treatment administrationGlobal eye-gaze patterns will be compared between the administration of oxytocin and placebo
Feature-specific eye gaze characteristics: differences between oxytocin and placebo treatment45-90 minutes after treatment administrationLocalized feature-specific eye gaze patterns will be compared between oxytocin and placebo treatment

Secondary

MeasureTime frameDescription
Global eye gaze characteristic - associations with autism traits45-90 minutes after treatment administrationWithin-subject differences in global eye gaze characteristics between the oxytocin and placebo administration will be examined for associations with individual differences in autism traits
Feature-specific eye gaze characteristics - associations with trait autism45-90 minutes after treatment administrationWithin-subject differences in localized feature-specific eye gaze characteristics between the oxytocin and placebo administration will be examined for associations with individual differences in autism traits

Countries

China

Contacts

Primary ContactKeith M Kendrick, PhD
k.kendrick.uestc@gmail.com86-28-61830811
Backup ContactBenjamin Becker, PhD
ben_becker@gmx.de86-28-61830988

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026