Identification of the Determinants of the Perceived Workload of Nurses (CHARMIREA)

March 25, 2026 updated by: Assistance Publique - Hôpitaux de Paris

Identification of the Determinants of the Perceived Workload of Intensive Care and Pediatric Continuous Monitoring Nurses

The purpose of this study is to identify the determinants of the perceived workload of intensive care and pediatric continuous monitoring nurses (factors liked to the care service, staff, patients treated)

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

In intensive care and pediatric continuous monitoring unit (RSCP), the workload of nurses (registered nurses) is high. It is important to distribute the workload correctly among caregivers in order to guarantee the quality and safety of care.

Workload can be measured by different means. The measure of the perceived workload has the advantage of taking into account not only the acts and care performed, but also the time pressure felt, the feeling of having been efficient in its task, the efforts made and the level of frustration felt.

Measuring the workload of RSCP registered nurses will help highlight the factors that may influence the workload. The aim is to allow an adequate distribution of patients between nurses, taking into account the determinants identified during this study.

Primary objective : Measure RSCP's nurses workload

Secondary objectives: Highlight the determinants of the overall perceived workload of RSCP nurses (organizational characteristics, of the individual, of the patient and of his entourage).

Highlight the determinants of each dimension of the perceived workload of RSCP nurses.

The calendar of data collection days will be defined by drawing lots. The day drawn for data collection will proceed normally, with no change in practice for nurses. A study investigator will inform the legal representative (s) of the possible data collection in their child that day and will trace their non-opposition in the medical file.

At the end of the day, registered nurses should collect data relating to family circles and individual characteristics. In addition, nurses must complete a NASA TLX grid for each patient treated during their working time. The grids will be assembled at the end of the day (around 7 p.m.) and handed over to an investigator. The same procedure will apply to the night shift, the grids will be handed over at 7 a.m. to an investigator.

In the following days, the principal investigator will collect the data related to the organizational characteristics and characteristics of the patients.

The perceived workload of nurses working in Intensive care and Continuous Monitoring Unit will be measured for each nurse who has at least 1 patient in charge during a period of 24 hours over 2 days (a day service and a night service, i.e. from 7 a.m. to 7 a.m. / D + 1 ), once a month for a year.

The measurement periods will be drawn at the rate of a period of 24 hours per month for one year, ie 12 periods in total.

Study Type

Observational

Enrollment (Actual)

484

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

      • Paris, France, 75015
        • Necker Enfants Malades hospital

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Nurses works in Pediatric Intensive care and Continuous Monitoring Unit of the Necker Hospital, AP-HP, Paris Child hospitalized in the Intensive care and Continuous Monitoring Unit of the Necker Hospital, AP-HP, Paris

Description

Inclusion Criteria:

  • Registered nurses from Pediatric Intensive care and Continuous Monitoring Unit agreeing to participate in the study,
  • Having at least one patient in charge over the period considered
  • Child regardless of age hospitalized in the Pediatric Intensive care and Continuous Monitoring unit.
  • Non-opposition of the legal representative (s) to the collection of data

Exclusion Criteria:

  • Nurse in job adaptation training
  • Interim nurse
  • Nurse not usually working in intensive care
  • Reference nurses of the service
  • Legal guardian of the child who doesn't speak or understand French

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Task Load indeX scale (TLX scale)
Time Frame: 1 day
TLX scale is a workload scale according to 6 dimensions: mental demands, physical demands, time pressure, performance, effort and frustration.Each dimension is evaluated on a 100-points scale. A total score from 0 to 600 points is obtained. A higher score means a worse outcome.
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Seniority in the profession
Time Frame: 1 day
Seniority in the profession in years Seniority in the service in years Age Previous patient management (at least once in the previous 12 months) Supervision of a student Tutoring a new nurse
1 day
Seniority in the service
Time Frame: 1 day
Seniority in the service in years Seniority in the service in years Age Previous patient management (at least once in the previous 12 months) Supervision of a student Tutoring a new nurse
1 day
Age of nurse
Time Frame: 1 day
Age of nurse in years Day / night work Number of patient transportations Reception of an incoming patient Participation in an ethics meeting
1 day
Age of nurse
Time Frame: 1 day
Age of nurse in years
1 day
Previous patient management
Time Frame: 1 day
Previous patient management (at least once in the previous 12 months)
1 day
Supervision of a student
Time Frame: 1 day
Supervision of a student (yes/no)
1 day
Tutoring a new nurse
Time Frame: 1 day
Tutoring a new nurse (yes/no)
1 day
Ratio patient/nurse
Time Frame: 1 day
Number of patient split by the number of nurse
1 day
Period of work
Time Frame: 1 day
Day / night work
1 day
Patient transport
Time Frame: 1 day
Number of patient transportations outside the ward.
1 day
New patient
Time Frame: 1 day
Reception of an incoming patient
1 day
Ethics meeting
Time Frame: 1 day
Participation of nurse to an ethics meeting
1 day
Age of patient
Time Frame: 1 day
Age of patient in years
1 day
Weight of patient
Time Frame: 1 day
Weight of patient in kilograms
1 day
Lengh of Hospitalisation
Time Frame: 1 day
Number of days in hospital
1 day
Glasgow score
Time Frame: 1 day
Glasgow score of patient. Scored on a total score from 3 to 15 points is obtained. A higher score means a better outcome.
1 day
Vascular supply
Time Frame: 1 day
Type of vascular catheter present on the patient
1 day
Supportive system
Time Frame: 1 day
Number of supportive systems necessary
1 day
Treatment
Time Frame: 1 day
Number of treatments administered / 24 hours
1 day
Resuscitation maneuver
Time Frame: 1 day
Resuscitation maneuver necessary (yes/no)
1 day
Death
Time Frame: 1 day
Death of patient (yes/no)
1 day
Family support
Time Frame: 1 day
Number of hours of presence of at least one of the two parents
1 day
Phone calls
Time Frame: 1 day
Number of phone calls from parents
1 day
Family interview
Time Frame: 1 day
Family interview realised ( Yes/No)
1 day

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Sophie CRETE, BSc nursing, Assistance Public-Hôpitaux de Paris
  • Study Chair: Medhi OUALHA, MD, PhD, Assistance Public-Hôpitaux de Paris

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

June 20, 2022

Primary Completion (Actual)

November 2, 2023

Study Completion (Actual)

November 2, 2023

Study Registration Dates

First Submitted

November 2, 2021

First Submitted That Met QC Criteria

November 19, 2021

First Posted (Actual)

December 1, 2021

Study Record Updates

Last Update Posted (Actual)

March 30, 2026

Last Update Submitted That Met QC Criteria

March 25, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • APHP211025
  • 2021-A01542-39 (Other Identifier: ID-RCB)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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