UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000059893 |
|---|---|
| Receipt number | R000068498 |
| Scientific Title | A Multi-center Pre-Post Intervention Study of Work Engagement Assessment and Organizational Improvement in an Intensive Care Unit |
| Date of disclosure of the study information | 2026/01/01 |
| Last modified on | 2025/11/26 18:21:03 |
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Basic information
Public title
A Multi-center Pre-Post Intervention Study of Work Engagement Assessment and Organizational Improvement in an Intensive Care Unit
Acronym
ICU Work Engagement Improvement Study
Scientific Title
A Multi-center Pre-Post Intervention Study of Work Engagement Assessment and Organizational Improvement in an Intensive Care Unit
Scientific Title:Acronym
ICU Work Engagement Improvement Study
Region
| Japan |
Condition
Condition
Work engagement of healthcare professionals
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to continuously measure Work Engagement (WE) in the Intensive Care Unit (ICU) using the Japanese version of the Utrecht Work Engagement Scale (UWES), and to implement an intervention package consisting of quantitative evaluation using the engagement visualization platform "Wevox" and organizational improvement activities (PDCA cycle) based on feedback. The effect of this intervention package on WE will be scientifically verified using a Multiple Interrupted Time Series Design.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Score of the Japanese version of Utrecht Work Engagement Scale (UWES) (Overall and 3 sub-factors)
Timepoint: Measured monthly throughout the observation, intervention, and autonomy verification periods.
Key secondary outcomes
1. Organizational cost indicators (monthly average overtime hours, sick leave days, turnover rate/transfer request rate)
2. Employee Net Promoter Score (eNPS)
3. Patient-related outcomes (satisfaction survey scores for patients discharged from ICU)
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Historical
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Educational,Counseling,Training
Type of intervention
| Other |
Interventions/Control_1
Name: Intervention Group Description: Quantitative evaluation of engagement factors using "Wevox" will be conducted during the intervention period. Based on the analysis results feedback at monthly meetings, PDCA cycle-based organizational improvement activities (factor analysis, planning, execution, and re-evaluation) will be implemented.
Interventions/Control_2
Interventions/Control_3
Interventions/Control_4
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10
Eligibility
Age-lower limit
| Not applicable |
Age-upper limit
| Not applicable |
Gender
Male and Female
Key inclusion criteria
Full-time nurses working in the Intensive Care Unit (ICU) of Kanazawa University Hospital and the ICU of Toyama Prefectural Central Hospital.
Key exclusion criteria
None (It is difficult to exclude specific subjects as the study is linked to organizational improvement activities implemented throughout the facility).
Target sample size
100
Research contact person
Name of lead principal investigator
| 1st name | Junichiro |
| Middle name | |
| Last name | Yokawa |
Organization
Kanazawa University Hospital
Division name
Intensive Care Unit
Zip code
920-8641
Address
13-1 Takara-machi, Kanazawa-shi, Ishikawa
TEL
0762652000
jun-jun-116@staff.kanazawa-u.ac.jp
Public contact
Name of contact person
| 1st name | Junichiro |
| Middle name | |
| Last name | Yokawa |
Organization
Kanazawa University Hospital
Division name
Intensive Care Unit
Zip code
920-8641
Address
13-1 Takara-machi, Kanazawa-shi, Ishikawa
TEL
0762652000
Homepage URL
jun-jun-116@staff.kanazawa-u.ac.jp
Sponsor or person
Institute
Kanazawa University
Institute
Department
Personal name
Funding Source
Organization
Kanazawa University
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Toyama Prefectural Central Hospital
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Kanazawa University
Address
13-1 Takara-machi, Kanazawa-shi, Ishikawa
Tel
0762652000
jun-jun-116@staff.kanazawa-u.ac.jp
Secondary IDs
Secondary IDs
NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW
Institutions
Institutions
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 01 | Month | 01 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Preinitiation
Date of protocol fixation
| 2025 | Year | 11 | Month | 20 | Day |
Date of IRB
Anticipated trial start date
| 2026 | Year | 01 | Month | 01 | Day |
Last follow-up date
| 2029 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Management information
Registered date
| 2025 | Year | 11 | Month | 26 | Day |
Last modified on
| 2025 | Year | 11 | Month | 26 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068498
