Clinical Trials Directory

Trials / Completed

CompletedNCT06605300

The Effects of Oxytocin and Vasopressin on Delta-beta Cross-frequency Coupling

The Modulatory Effects of Oxytocin and Vasopressin on Delta-beta Cross-frequency Coupling

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
120 (actual)
Sponsor
University of Electronic Science and Technology of China · Academic / Other
Sex
All
Age
18 Years – 30 Years
Healthy volunteers
Accepted

Summary

The main aim of the study is to investigate whether intranasal oxytocin and vasopressin have effects on delta-beta cross-frequency coupling under resting-state and task conditions.

Detailed description

A double-blinded, placebo-controlled, between-subject design is employed in this study. In a randomized order, a total of 120 healthy males and females are instructed to self-administer intranasal spray of oxytocin, vasopressin, or placebo. (1) 15-minute resting-state EEG data are collected 35 minutes after treatment. (2) Participants complete tasks including Stroop, GO/NOGO, and anxiety induction with behavioral (response time, accuracy, or rating) and EEG data being collected. Personality traits of subjects are assessed using validated Chinese version questionnaires including the Beck Depression Inventory (BDI-II), State-Trait Anxiety Inventory (STAI), Autism Spectrum Quotient (ASQ), and Adult ADHD Self-Report Scale (ASRS-v1.1). Participants are asked to complete Positive and Negative Affect Schedule (PANAS) when they just arrive, before resting state and after the tasks. Three blood samples (5 ml) are collected into 6 ml ETDA tubes when participants just arrive, before resting state recording and after all of the tasks.

Conditions

Interventions

TypeNameDescription
DRUGIntranasal Oxytocin (IN-OXT)Subject assigned to receive intranasal administration of oxytocin (24 IU).
DRUGIntranasal Vasopressin (AVP)Subjects assigned to receive intranasal administration of vasopressin (20 IU).
DRUGIntranasal PlaceboSubjects assigned to receive intranasal administration of placebo.

Timeline

Start date
2024-10-02
Primary completion
2025-07-28
Completion
2025-08-12
First posted
2024-09-20
Last updated
2025-10-03

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06605300. Inclusion in this directory is not an endorsement.