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Effect of a musical intervention on tolerance and efficacy of non-invasive ventilation in the ICU: study protocol for a randomized controlled trial (MUSique pour l'Insuffisance Respiratoire Aigue - Mus-IRA).

Authors :
Messika, Jonathan
Hajage, David
Panneckoucke, Nataly
Villard, Serge
Martin, Yolaine
Renard, Emilie
Blivet, Annie
Reignier, Jean
Maquigneau, Natacha
Stoclin, Annabelle
Puechberty, Christelle
Guétin, Stéphane
Dechanet, Aline
Fauquembergue, Amandine
Gaudry, Stéphane
Dreyfuss, Didier
Ricard, Jean-Damien
Source :
Trials. 9/13/2016, Vol. 17, p1-13. 13p. 3 Diagrams, 1 Chart.
Publication Year :
2016

Abstract

<bold>Background: </bold>Non-invasive ventilation (NIV) tolerance is a key factor of NIV success. Hence, numerous sedative pharmacological or non-pharmacological strategies have been assessed to improve NIV tolerance. Music therapy in various health care settings has shown beneficial effects. In invasively ventilated critical care patients, encouraging results of music therapy on physiological parameters, anxiety, and agitation have been reported. We hypothesize that a musical intervention improves NIV tolerance in comparison to conventional care. We therefore question the potential benefit of a receptive music session administered to patients by trained caregivers ("musical intervention") to enhance acceptance and tolerance of NIV.<bold>Methods/design: </bold>We conduct a prospective, three-center, open-label, three-arm randomized trial involving patients in the intensive care unit (ICU) who require NIV, as assessed by the treating physician. Participants are allocated to a "musical intervention" arm ("musical intervention" applied during all NIV sessions), to a "sensory deprivation" arm (sight and hearing isolation during all NIV sessions), or to the control group. The primary endpoint is the change in respiratory comfort (measured with a digital visual scale) before the initiation and after 30 minutes of the first NIV session. The evaluation of the primary endpoint is performed blindly from the treatment group. Secondary endpoints include changes in respiratory and cardiovascular parameters during NIV sessions, the percentage of patients requiring endotracheal intubation, day-90 anxiety/depression and health-related quality of life, post-trauma stress induced by NIV, and the overall assessment of NIV. The follow-up for each participant is 90 days. We expect to randomize a total of 99 participants.<bold>Discussion: </bold>As music intervention is a simple and easy-to-implement non-pharmacological technique, efficacious in reducing anxiety in critically ill patients, it appeared logical to assess its efficacy in NIV, one of the most stressful techniques used in the ICU. Patient centeredness was crucial in choosing the outcomes assessed.<bold>Trial Registration: </bold>ClinicalTrials.gov: NCT02265458 . Registered on 25 August 2014. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17456215
Volume :
17
Database :
Academic Search Index
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
118127003
Full Text :
https://doi.org/10.1186/s13063-016-1574-z