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The Effects of Vasopressin on Attention Control

The Effects of Vasopressin on Attention Control: An Eye-tracking Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04493554
Enrollment
89
Registered
2020-07-30
Start date
2020-07-28
Completion date
2021-01-01
Last updated
2021-01-07

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 present study is to investigate whether intranasal vasopressin (20IU) could influence attention control in a social-emotional saccade/antisaccade eye-tracking paradigm.

Detailed description

A number of previous studies have reported vasopressin's effect on human social behavior and social cognition, although it remains unclear whether vasopressin could modulate attention allocation including stimulus-driven bottom-up control and goal-directed top-down control. In the current randomized, between-subject, placebo controlled study, 89 healthy male subjects will be recruited and receive either vasopressin (20 IU) or placebo control administered intranasally. 45 minutes after treatment subjects will be required to complete a social-emotional saccade /antisaccade eye-tracking paradigm. The 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 vasopressin.

Interventions

DRUGVasopressin

Administration of vasopressin (20 IU) intranasally

DRUGPlacebo

Administration of placebo intranasally

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

* 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 vasopressin * Contra-indications for eye-tracking data acquisition

Design outcomes

Primary

MeasureTime frameDescription
Effect of vasopressin 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 vasopressin and placebo treatment conditions
Effect of vasopressin 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 vasopressin and placebo treatment conditions

Secondary

MeasureTime frameDescription
Emotion-specific effects of vasopressin 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 vasopressin and placebo treatment conditions
Emotion-specific effects of vasopressin 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 vasopressin and placebo treatment conditions

Countries

China

Outcome results

None listed

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