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Clinical Trials/NCT04493515
NCT04493515
Unknown
Not Applicable

Oral Oxytocin's Effects on Attention Control: An Eye-tracking Study

University of Electronic Science and Technology of China1 site in 1 country80 target enrollmentJuly 28, 2020

Overview

Phase
Not Applicable
Intervention
Oral Placebo
Conditions
Healthy
Sponsor
University of Electronic Science and Technology of China
Enrollment
80
Locations
1
Primary Endpoint
Effect of oral oxytocin administration on saccade/antisaccade latencies towards social (facial) versus non-social (shape) stimuli
Last Updated
5 years ago

Overview

Brief Summary

The main aim of the study is to investigate whether orally administered oxytocin (24IU) could modulate attention control using a social-emotional saccade/antisaccade eye-tracking paradigm.

Detailed Description

Numerous studies have reported the effect of intranasally administered oxytocin on attentional processing including stimulus-driven bottom-up processing and top-down goal-directed inhibitory control. However, it is unclear whether the functional effects are mediated by the peptide directly entering the brain or indirectly via raising peripheral concentrations. One possible method of producing a similar pattern of increased peripheral oxytocin concentrations but without the possibility of direct entry into the brain would be to administer the peptide lingually. In the present double-blind, between-subject, placebo-controlled study, 80 healthy male subjects will be recruited and receive either oxytocin (24IU) or placebo control administered orally (lingual). 45 minutes after treatment subjects are required to complete a social-emotional saccade/antisaccade eye-tracking paradigm. This paradigm uses social (happy, sad, angry, fear, and neutral faces) as well as non-social (oval shapes) stimuli to explore social- and emotion-specific effects of orally administered oxytocin.

Registry
clinicaltrials.gov
Start Date
July 28, 2020
End Date
December 31, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
University of Electronic Science and Technology of China
Responsible Party
Principal Investigator
Principal Investigator

Keith Kendrick

Professor

University of Electronic Science and Technology of China

Eligibility Criteria

Inclusion Criteria

  • Male, healthy participants
  • Non smokers

Exclusion Criteria

  • Previous or current medical, psychiatric, neurological disorder
  • Regular medication
  • Use of any psychoactive substances in the 24 hours before experiment
  • Contra-indications for oxytocin
  • Contra-indications for eye-tracking data acquisition

Arms & Interventions

Oral Placebo

Placebo orally (24 IU, identical ingredients, except the active agent)

Intervention: Oral Placebo

Oral Oxytocin

Oxytocin orally (24 IU)

Intervention: Oral Oxytocin

Outcomes

Primary Outcomes

Effect of oral oxytocin administration on saccade/antisaccade latencies towards social (facial) versus non-social (shape) stimuli

Time Frame: 45 minutes - 100 minutes after treatment

Comparison between social-specific saccade/antisaccade latencies (in milliseconds) between the oxytocin and placebo treatment conditions

Effect of oral oxytocin administration on error rates of saccade/antisaccade for social (facial) versus non-social (shape) stimuli

Time Frame: 45 minutes - 100 minutes after treatment

Comparison between social-specific error rates of saccade/antisaccade between the oxytocin and placebo treatment conditions.

Secondary Outcomes

  • Emotion-specific effects of oral oxytocin administration on saccade/antisaccade latencies towards the separate facial emotions(45 minutes - 100 minutes after treatment)
  • Emotion-specific effects of oral oxytocin administration on saccade/antisaccade error rates for the separate facial emotions(45 minutes - 100 minutes after treatment)

Study Sites (1)

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