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Clinical Trial Summary

This study is a parallel arm, double-blind, randomized, controlled clinical trial to assess the safety and efficacy of an experimental software program designed to improve cognitive functions versus a computer-based software control. Both the study and the software being investigated meet the criteria of Non-Significant Risk.


Clinical Trial Description

The primary objective of this study is to evaluate the effects of combination of mindfulness training (MT) and adaptive cognitive training (CT) on the cognitive abilities, functional status and quality of life of soldiers and veterans diagnosed with traumatic brain injury (TBI, also referred to as a concussion, or blast exposure), as compared to a computer-based control. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02922569
Study type Interventional
Source Posit Science Corporation
Contact
Status Completed
Phase N/A
Start date March 31, 2017
Completion date September 14, 2020

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