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Clinical Trial Summary

This is a prospective, home-based, interventional clinical study in which 6 subjects will be enrolled. Six (6) subjects who suffer from post-traumatic stress disorder will receive treatment using the NeuroGlove.


Clinical Trial Description

This is a prospective, home-based, interventional clinical study in which 6 subjects will be enrolled. Six (6) subjects who suffer from post-traumatic stress disorder will receive treatment using the NeuroGlove. There will be a single cohort in the study consisting of the subjects with PTSD who will receive treatment with NeuroGlove. The trial is intended to evaluate the impact of the device use on active PTSD symptoms and subject sense of well-being. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06050590
Study type Interventional
Source NeuroGlove LLC
Contact
Status Active, not recruiting
Phase N/A
Start date August 14, 2023
Completion date September 1, 2024

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