Perception of Stress and Safety Culture: Analysis of Critical Factors in Healthcare (SICURES) (SICURES)

January 14, 2026 updated by: Centro Cardiologico Monzino

Percezione Dello Stress e Cultura Della Sicurezza: Analisi Dei Fattori Critici in Ambito Sanitario (SICURES)

The study adopts an observational design, based on a sample of 143 healthcare professionals, using two validated anonymous questionnaires: the Perceived Stress Scale (PSS-10) to measure perceived stress levels and the Hospital Survey on Patient Safety Culture 2.0 (SOPS AHRQ) to assess perceptions of patient safety culture.

Data collection will take place at a single point in time and without external intervention, on a sample of healthcare professionals belonging to the various hospital operating units of the CCM.

Objectives (primary and secondary):

  • Primary: This study aims to analyze whether the levels of risk management perceived by healthcare professionals are predictive of perceived stress levels in the same clinical context.

  • Secondary:

    • Assess the level of stress perceived by healthcare professionals
    • Explore the perception of patient safety culture
    • Analyze the correlation between perceived stress and safety culture in hospital settings
    • Identify possible critical areas or organizational factors that contribute to the onset of stress and influence the perception of safety in care

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

164

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Italy
    • MI
      • Milan, MI, Italy, 20138
        • Irrcs Centro Cardiologico Monzino

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

healthcare professionals of CCM DAPS'

Description

Inclusion Criteria:

  • healthcare professionals of CCM DAPS'

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
healthcare professionals

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
relationship betweemn levels of risk management perceived and perceived stress levels
Time Frame: July 2025 - October 2025
This study aims to analyze whether the levels of risk management perceived by healthcare professionals are predictive of perceived stress levels in the same clinical context.
July 2025 - October 2025

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Centro Cardiologico Monzino

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 14, 2025

Primary Completion (Actual)

September 10, 2025

Study Completion (Actual)

September 10, 2025

Study Registration Dates

First Submitted

December 15, 2025

First Submitted That Met QC Criteria

January 7, 2026

First Posted (Estimated)

January 14, 2026

Study Record Updates

Last Update Posted (Actual)

January 15, 2026

Last Update Submitted That Met QC Criteria

January 14, 2026

Last Verified

July 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • L2-376

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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