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Effect of Transcutaneous Auricular Neurostimulation on Cognitive Performance in a Laboratory Model of Acute Stress Reaction — ASR  

Cognitive Performance Clinical Trial

Official title:
Effect of Transcutaneous Auricular Neurostimulation on Cognitive Performance in a Laboratory Model of Acute Stress Reaction

Clinical Trial Summary

The objective of this study is to test the effects of transcutaneous auricular neurostimulation (tAN) in treating or preventing performance degradation after an acute stressor.

Clinical Trial Description

This study is designed as a randomized, double-blind, sham-controlled trial. Sixty healthy, able-bodied participants will be randomized 1:1:2:2 into one of four experimental groups: Group 1: Active tAN for prophylactic treatment prior to acute stress exposure (N=10) Group 2: Sham stimulation for prophylactic treatment prior to acute stress exposure (N=10) Group 3: Active tAN for acute treatment during acute stress exposure (N=20) Group 4: Sham stimulation for acute treatment during acute stress exposure (N=20) Participants will complete a baseline performance of three tasks. tAN treatment will then be administered prior to or during an acute stress test. Participants will complete the same three tasks preformed at baseline. In addition to the tAN therapy earpiece, subjects will have biosensors attached to them to collect biomarker information. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06390267
Study type Interventional
Source Spark Biomedical, Inc.
Contact Caroline Benner
Phone 817-933-2727
Email caroline.benner@sparkbiomedical.com
Status Not yet recruiting
Phase N/A
Start date August 2024
Completion date April 30, 2025
View Details
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