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Clinical Trial Summary

The purpose of this study is to assess the use of an audio recording containing positive suggestion as a means to provide needed psychological support to critically ill patients in a feasible and reliable manner.


Clinical Trial Description

Following screening and consenting processes, patients will be randomized to enroll in interventional or control groups. The interventional group will listen to an audio recording of psychological support based on positive suggestion for about 30 min each day via headphones. At the time of ICU discharge, patients will be administered validated questionnaires to screen for symptoms of anxiety/depression (HADS), PTSD (IES-r), cognitive dysfunction (MOCA-blind), as well as evaluation of health status (EQ-5D). Six months post ICU discharge, patients will again be contacted and repeat the assessment with above questionnaires. Scores on the questionnaires will be compared between the groups at the two times points. Patient demographic data will also be obtained and assessed to contextualize study findings. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04437095
Study type Interventional
Source Mayo Clinic
Contact Lioudmila V Karnatovskaia, MD
Phone 507 284-2511
Email Karnatovskaia.Lioudmila@mayo.edu
Status Recruiting
Phase N/A
Start date August 17, 2020
Completion date July 2025

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