Effectiveness of an Interventional Intervention in Improving the Work Environment of Nurses and Nursing Assistants in the Hospital

May 29, 2026 updated by: Estel Curado Santos, Universitat Internacional de Catalunya

The goal of this interventional study is to evaluate the effectiveness of a training course on a healthy work environment for nurses and nursing assistants in a hospital. The main questions it aims to answer are:

  • To evaluate the effectiveness of a training course on a healthy work environment
  • To know the perception of nursing and nursing assistants on what is needed to have a healthy work environment, what elements it should contain and whether it has changed after the course has been completed

Participants in the intervention group will receive the training course and the control group will not. Researchers will compare intervention group with control group to see if the training course on healthy work environment is effective.

Study Overview

Detailed Description

Concurrent mixed study consisting of different phases in which the qualitative and quantitative parts will be interspersed. The qualitative part will include focus groups, and the quantitative part will be a controlled non-randomised experimental study by convenience sampling according to hospital unit and professional category (nurses and nursing assistants). Multicenter study carried out at Hospital General de Granollers and the Consorci Sanitari de Terrassa in nursing professionals and nursing assistants with one year of experience working in the hospital in any of the hospitalization services or special services. Once the subjects have been included in the study, they will be assigned in each group (control group and intervention group) through a stratification by quotas following the same criteria as in the sampling. The intervention group will receive training, and the control group will not. The training will be based on the American Association of Critical Care Nurses standards on a healthy work environment. In both groups, the same data will be collected at different times (before and just after the training, at 6 months and 12 months post-training). The focus groups will not be conducted in the control group after the training. Work environment, burnout, intention to leave the job and staff engagement will be assessed.

Study Type

Interventional

Enrollment (Actual)

139

Phase

  • Not Applicable

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

    • Barcelona
      • Granollers, Barcelona, Spain, 08402
        • Hospital General de Granollers
      • Terrassa, Barcelona, Spain, 08227
        • Consorci Sanitari de Terrassa

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Voluntary acceptance to participate in the study
  • Having worked at least one year in the hospital

Exclusion Criteria:

  • Nursing supervisors/nursing assistants or people with management positions
  • Professionals working in more than one care center
  • Professionals working in the outpatient area

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

  • Primary Purpose: Other
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Group
Experimental: Intervention Group
Participants in the intervention group will receive the training course on healthy work environment

Once the participants have been included in the study, they will be assigned to each group; control group and intervention group by convenience sampling. Baseline data will be collected in both groups. At this time, questionnaires will be collected in both populations and focus groups will be conducted in the professionals assigned to both groups. Once the data have been obtained, the intervention group will conduct the training course.

After the training, data will be collected again at three different times: 1) Right after the training: questionnaires and focus group will be collected from intervention group professionals; 2) 6 months after the training: questionnaires will be collected from control group and intervention group; 3) 12 months after the training: questionnaires will be collected and focus groups will be conducted in both groups.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Work Environment (1)
Time Frame: 6 months
The Practice Environment Scale-Nursing Work Index (PES-NWI) will be used to assess the work environment. The PES-NWI is used to measure day-to-day aspects of organizational culture and climate, and is more frequently used in European studies. The PES-NWI is Likert-type with scores from 1 to 4 (strongly disagree - strongly agree). Three category variable indicating favorable, mixed, or unfavorable practice environments: favorable = four or more subscale means exceed 2.5; mixed = two or three subscale means exceed 2.5; unfavorable = zero or one subscales exceed 2.5.
6 months
Work Environment (2)
Time Frame: 6 months
The American Association of Critical Care Nurses (AACN) questionnaire will be used to assess the work environment. The AACN questionnaire is much broader and covers other aspects related to the work environment. The AACN scoring guidelines for the assessment are: 1.00-2.99 - Needs Improvement 3.00-3.99 - Good 4.00-5.00 - Excellent.
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Burnout
Time Frame: 1 year
Questionnaire for the Assessment of Job Burnout Syndrome (CESQT) will be used to evaluate the burnout syndrome in professionals who care for people.
1 year
Intention to leave
Time Frame: 1 year
The American Association of Critical Care Nurses questionnaire will be used to assess the intention to leave of participants.
1 year
Focus groups
Time Frame: 1 year
Professionals participating in the study will be invited to collaborate in focus groups depending on the time of the study. These will take place at different times and will have different objectives. Before the intervention (control group and intervention group), they will focus on what they consider to be a healthy work environment and what elements they identify it should contain. After the intervention (only intervention group), we will explore how their perception of what a healthy work environment is has changed. At 12 months (control group and intervention group), we will explore whether there has been any change during this time in the work environment and the perceptions about the actions they consider that the institution and/or professionals could take to improve the work environment.
1 year
Engagement
Time Frame: 1 year
Utrecht work engagement scale (UWES) will be use to assess the engagement. The UWES contais 17 items; 6 items in reference to vigor (item 1, ,4, 8, 12, 15, 17), 5 items to dedication (item 2, 5, 7, 7, 10 13) and 6 items to absorption (item 3, 6, 9, 11, 14, 16). It is a frequency scale with 6 response options from 0 (never) to every day (6).
1 year
Work environment (1)
Time Frame: 1 year
The Practice Environment Scale-Nursing Work Index (PES-NWI) will be used to assess the work environment. The PES-NWI is used to measure day-to-day aspects of organizational culture and climate, and is more frequently used in European studies. The PES-NWI is Likert-type with scores from 1 to 4 (strongly disagree - strongly agree). Three category variable indicating favorable, mixed, or unfavorable practice environments: favorable = four or more subscale means exceed 2.5; mixed = two or three subscale means exceed 2.5; unfavorable = zero or one subscales exceed 2.5.
1 year

Collaborators and Investigators

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

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)

October 5, 2022

Primary Completion (Actual)

July 26, 2023

Study Completion (Actual)

April 30, 2025

Study Registration Dates

First Submitted

January 29, 2024

First Submitted That Met QC Criteria

January 29, 2024

First Posted (Actual)

February 6, 2024

Study Record Updates

Last Update Posted (Actual)

June 3, 2026

Last Update Submitted That Met QC Criteria

May 29, 2026

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • INF-2022-01
  • 20212013 (Registry Identifier: Hospital General de Granollers)
  • 02-23-305-060 (Registry Identifier: Consocri Sanitari de Terrassa)
  • PR-551/2022 (Other Grant/Funding Number: Official College of Nurses of Barcelona)

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

product manufactured in and exported from the U.S.

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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