临床试验/NCT07606573

NCT07606573招募中不适用

The SEAS Study: Sensory Engagement and Activation During Noninvasive Stimulation

University of Minnesota3 个研究点分布在 1 个国家目标入组 40 人开始时间: 2026年6月8日最近更新: 2026年6月11日

干预措施

试验速览

阶段: 不适用
状态: 招募中
发起方: University of Minnesota
入组人数: 40
试验地点: 3

研究概览研究设计入排标准研究组 & 干预措施研究者研究点记录与标识符相似试验

研究概览

简要总结

Early feasibility study to establish quantitative physiological markers correlated with noninvasive stimulation.

详细描述

This pilot early feasibility study in healthy participants is intended to establish quantitative physiological markers of cortical and autonomic modulation evoked by noninvasive electrical and/or ultrasound stimulation of the nervous system.

研究设计

研究类型: Interventional
分配方式: Randomized
干预模型: Crossover
主要目的: Basic Science
盲法: Single (Participant)

入排标准

年龄范围: 18 Years 至 65 Years（Adult, Older Adult）
性别: All
接受健康志愿者: 是

入选标准

•Able to provide written informed consent in English.
•Willing and able to complete study procedures (e.g., ~1-hour sessions with non-invasive recordings, ~3-hour visit).

排除标准

•History of neurological disorders (e.g., epilepsy, migraines) or psychiatric conditions requiring medication.
•Active implanted medical devices (e.g., pacemakers, cochlear implants) or metal in the neck/forearm that could interfere with stimulation or recordings.
•Skin conditions or open wounds at stimulation sites (cervical neck, forearm).
•Women who are pregnant or breastfeeding.
•Current use of medications affecting autonomic or cortical function (e.g., beta-blockers, sedatives).
•Inability to sit still for recordings or understand instructions (e.g., due to severe vision/hearing impairment).

研究组 & 干预措施

Acute electrical stimulation session versus no stimulation (sham).

Experimental

干预措施: External electrical stimulation (Device)

Acute ultrasound stimulation session versus no stimulation (sham).

Experimental

干预措施: Ultrasound stimulation (Device)

研究者

发起方

University of Minnesota

申办方类型

Other

责任方

Sponsor

研究点 (3)

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