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Oral Oxytocin's Effects on Attention Control

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04493515
Enrollment
80
Registered
2020-07-30
Start date
2020-07-28
Completion date
2021-12-31
Last updated
2020-07-30

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

Conditions

Healthy

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.

Interventions

Administration of oxytocin orally (24 IU)

DRUGOral Placebo

Administration of placebo orally (24 IU)

Sponsors

University of Electronic Science and Technology of China
Lead SponsorOTHER

Study design

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

Intervention model description

Between-subject randomized placebo-controlled double-blind pharmacological eye-tracking design

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Effect of oral oxytocin administration on saccade/antisaccade latencies towards social (facial) versus non-social (shape) stimuli45 minutes - 100 minutes after treatmentComparison 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) stimuli45 minutes - 100 minutes after treatmentComparison between social-specific error rates of saccade/antisaccade between the oxytocin and placebo treatment conditions.

Secondary

MeasureTime frameDescription
Emotion-specific effects of oral oxytocin administration on saccade/antisaccade latencies towards the separate facial emotions45 minutes - 100 minutes after treatmentComparison between emotion-specific saccade/antisaccade latencies (in milliseconds) between the oxytocin and placebo treatment conditions
Emotion-specific effects of oral oxytocin administration on saccade/antisaccade error rates for the separate facial emotions45 minutes - 100 minutes after treatmentComparison between emotion-specific saccade/antisaccade error rates between the oxytocin and placebo treatment conditions

Countries

China

Contacts

Primary ContactZhuang Qian, MD
zq19910362@126.com13086663679
Backup ContactXu Xiaolei, PhD
rabby_uestc@outlook.com18780140034

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026