Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Managing alarm noise in intensive care units to improve patient safety

Official title: Impact of an Alarm Management Protocol on Noise Pollution and Patient Safety in Intensive Care Units

Run by Centre Hospitalier Universitaire de Saint Etienne · NCT06175091 · Data updated 2026-11-12

This study is testing a new way to manage alarm sounds in intensive care units to see if it can make the environment safer and less stressful for patients and staff.

More Intensive Care Unit trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment514 (estimated)
SponsorCentre Hospitalier Universitaire de Saint Etienne
Academic / other
Locations1 site (Saint-Etienne)
StatusRecruiting
StartedFebruary 8, 2024
Main results expectedJanuary 31, 2028
Study endsFebruary 28, 2028
Registry record updatedMarch 10, 2026
Trial IDNCT06175091 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults aged 18 and older who are admitted to the intensive care unit at the Saint-Etienne University Hospital.

Probably not a fit

Patients who are pregnant, nursing, or under legal guardianship will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of a restrictive alarm management protocol in intensive care units to reduce unnecessary noise pollution and enhance patient safety. It addresses the issue of alarm fatigue, where excessive alarms lead to stress for patients and desensitization among nursing staff, potentially compromising care quality. By analyzing alarm signals and implementing a more rational alarm strategy, the study aims to improve the overall environment for both patients and healthcare providers.

Why it matters

Potential benefit: If successful, this approach could significantly enhance patient comfort and safety in intensive care settings.

How similar studies have gone: Previous studies have indicated that alarm management strategies can improve patient outcomes, suggesting that this approach may yield positive results.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient aged ≥ 18 years
* Patient admitted to the intensive care unit of the ST-ETIENNE University Hospital
* Patient affiliated or entitled to a social security system
* Patient having received informed information about the study and having co-signed, with the investigator, a consent to participate in the study or, for patients who are unable to consent due to health condition, a trusted person/family member who has been informed about the study and has who has co-signed, with the investigator, a consent to participate

Exclusion Criteria:

* Pregnant and nursing women
* Persons of legal age under guardianship

Where it's running

  • CHU de Saint-Etienne
    Saint-Etienne, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.