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Oxytocin Modulates Eye Gaze Behavior During Social Processing

U

University of Electronic Science and Technology of China

Status

Unknown

Conditions

Healthy

Treatments

Drug: intranasal placebo
Drug: intranasal oxytocin

Study type

Interventional

Funder types

Other

Identifiers

NCT03293511
UESCT_neuSCAN_42

Details and patient eligibility

About

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

Full 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.

Enrollment

40 estimated patients

Sex

Male

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

40 participants in 2 patient groups

Order of administration: oxytocin - placebo
Experimental group
Description:
Participants first receive oxytocin (24 IU). After a washout period of 2 weeks, they receive placebo nasal spray
Treatment:
Drug: intranasal placebo
Drug: intranasal oxytocin
Order of administration: placebo - oxytocin
Experimental group
Description:
Participants first received placebo nasal spray. After a washout period of 2 weeks, they then receive oxytocin (24 IU).
Treatment:
Drug: intranasal placebo
Drug: intranasal oxytocin

Trial contacts and locations

2

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Central trial contact

Benjamin Becker, PhD; Keith M Kendrick, PhD

Data sourced from clinicaltrials.gov

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