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Early-feasibility Study to Evaluate Usability and Safety of the Watch-Transcutaneous Electrical Acustimulation (TEA) Device

Healthy Clinical Trial

Official title:
Early-feasibility Study to Evaluate Usability and Safety of the Watch-Transcutaneous Electrical Acustimulation (TEA) Device

Clinical Trial Summary

This project is being completed to test the usability and safety of the Watch-Transcutaneous Electrical Acustimulation (TEA) Device. This is a pilot study that will lead to future projects for cancer patients that may experience chemotherapy-induced symptoms.

Clinical Trial Description

This project will include three different aims (aim three is a clinical trial) and will be funded by the National Institute of Health (NIH). In aims 1 and 2 the device hardware and device application will be developed and will not be included in this registration as these are not clinical trials. However, aim three is being registered early in the project in order to obtain the Notice of Award (NOA) funding from the NIH. Once the NOA has been obtained the registration will be updated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06366074
Study type Interventional
Source University of Michigan
Contact Colin Burnett
Phone 734-647-2806
Email bucolin@umich.edu
Status Not yet recruiting
Phase N/A
Start date August 2024
Completion date August 2025
View Details
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