CHU de Saint-Etienne
Saint-Etienne, 42055, France
Location status: Recruiting
NCT Number: NCT06175091
Resuscitation patients are monitored for various physiological parameters. When these parameters exceed abnormal thresholds, an audible alarm is triggered. Given the complexity of physiological situations and the number of monitored parameters, the number of alarms within an intensive care unit is significant. In the literature, the number ranges from 100 to 350 alarms per patient per day. Among these alarms, 74 to 99% are deemed irrelevant as they provide false or insignificant information. This study will enable to assess the efficacy of a restrictive protocol for managing alarms as a means of rationalizing their use.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Saint-Etienne, 42055, France
Location status: Recruiting
The large volume of unnecessary alarms has multiple negative repercussions. Firstly, the excessively loud sound environment present in most resuscitation services causes stress and discomfort for both patients and caregivers. Additionally, nurses become desensitised and less responsive when the number of alarms is high, particularly if many of them are ultimately pointless. Finally, multiple interruptions of tasks associated with alarms that require responses are sources of errors in the execution of care and medication preparation.
These interruptions contribute to a phenomenon known as "alarm fatigue", which many authorsand health authorities consider a threat to patient safety.The intensive care unit of the Saint-Etienne University Hospital has had a long-standing interest in this topic, and has a computerized data collection tool that permits exhaustive analysis of all alarm signals originating from each resuscitation bed.
This study will enable to assess the efficacy of a restrictive protocol for managing alarms as a means of rationalizing their use.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
alarm management left to the discretion of the nurse in charge of the patient
more restrictive protocol for the use of alarms
Time frame: 1 month
An efficiency criterion: the number of alarms per patient per day
Time frame: 1 month
A safety criterion: the length of time patients have potentially dangerous heart rate, blood pressure or oxygen saturation values.
Time frame: 1 month
Incidence of serious adverse events
Time frame: 1 month
Alarm response time: the time between the alarm being triggered and the acoustic signal being silenc
Time frame: 1 month
Evaluation of patient perception using the Discomforts of intensive care patients questionnaire. The Discomforts of intensive care patients questionnaire validated in intensive care and in French, assesses 16 sources of discomfort, including noise. The questionnaire is given to patients before they are discharged from intensive care. The questionnaire scores range from 0 to 100, with the highest score indicating maximum discomfort.
Time frame: 7 days
Sound level measurement using a sound level meter. A measuring instrument will be placed in the rooms of the patients included during the day for 4 consecutive hours on day 1, 3 and 7. This part of the study will be carried out in conjunction with occupational medicine and the Quality, Risk Management and Patient Experience Department, which already carry out this type of measurement as part of their assessment of working conditions.
Interested in participating?
Request InfoCentre Hospitalier Universitaire de Saint Etienne
Other
Acronym: REALARM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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