- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06244784
Effectiveness of an Interventional Intervention in Improving the Work Environment of Nurses and Nursing Assistants in the Hospital
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
Status
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Barcelona
-
Granollers, Barcelona, Spain, 08402
- Hospital General de Granollers
-
Terrassa, Barcelona, Spain, 08227
- Consorci Sanitari de Terrassa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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