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Clinical Trial Summary

1. To determine the effects of tDCS on subjective measures of sleepiness in night-shift workers with shift work disorder. 2. To determine the effects of transcranial direct current stimulation (tDCS) on vigilance in night-shift workers with shift work disorder.


Clinical Trial Description

This is a preliminary single-arm study. The study will last up to 6 weeks including the screening period. Subjects will receive active tDCS for 30 minutes before their scheduled work hours at least 3x/week for two consecutive weeks. Outcome measures will include: psychomotor vigilance test (PVT) and the Karolinska Sleepiness Scale (KSS)25,26 which will be obtained during the shift work. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03879044
Study type Interventional
Source Ohio State University
Contact
Status Terminated
Phase N/A
Start date March 20, 2019
Completion date June 20, 2020

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