- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07500688
Empowering Nursing Newcomers Program (EMPOWER)
Empowering Nursing Newcomers
In the Netherlands, more and more nurses with an international background, such as refugees and migrants, are starting to work in healthcare. Many of them already have a lot of knowledge and experience, but it is not always easy to quickly adapt to the Dutch healthcare system and a new language. That is why the programme "Empowering Newcomers Nurses" was developed.
This study aims to better understand how the programme works in practice. Participants and supervisors will be asked about their experiences to identify what works well and what could be improved. The costs and the benefits are also taken into account. The results will be used to further improve the programme.
It will also be assessed whether the work environment is inclusive and welcoming for participants. For example, this may involve (unconscious) microaggressions, exclusion, or negative comments, including those that may be discriminatory or racist. By making these experiences visible, it becomes easier to address them and make improvements. In addition, scientific articles will be published so that other hospitals can also learn from these insights.
Who can participate? Nursing newcomers who are already participating in the programme or who will start the programme soon are invited to take part in the study. Sometimes participants with another paramedical background also take part. For this study, it is expected that over a period of 9 years about 160-230 participants will take part in total, of whom 120-150 will be from the northern region of the Netherlands. This number is not strictly required, but it helps to better understand how the programme works, what works well, and where improvements may be possible. In this way, a more complete picture of the programme can be obtained.
Study Overview
Status
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Arthur Wijsmuller, MD PhD
- Phone Number: +31625646662
- Email: a.r.wijsmuller@umcg.nl
Study Contact Backup
- Name: Petra Veltman
- Phone Number: +31629442932
- Email: p.m.v.veltman@umcg.nl
Study Locations
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Provincie Groningen
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Groningen, Provincie Groningen, Netherlands, 9713 GZ
- Recruiting
- University Medical Center Groningen
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Contact:
- Arthur Wijsmuller, MD PhD
- Phone Number: +31625646662
- Email: a.r.wijsmuller@umcg.nl
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Contact:
- Petra Veltman
- Phone Number: +31629442932
- Email: p.m.v.veltman@umcg.nl
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- refugee or migrant with a nursing background or other paramedical background and sufficient indications that the relevant hospital department is prepared to cooperate in a fast-track integration trajectory
- holding at least a diploma equivalent to the Dutch MBO-4 level
- having practical experience, preferably in a hospital setting
- residence in one of the three northern provinces
- sufficient learning capacity to participate in a language course at the University of Groningen's Language Centre based on the intake and, if available, a study skills test
- a successful application interview
Exclusion Criteria:
- diploma lower than Dutch MBO-4 level
- refugee or migrant with a background as medical doctor
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Nursing newcomers
Fasttrack integration trajectory
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Proportion participants progressing as planned or successfully completing the program
Time Frame: From enrolment through programme completion (up to 36 months)
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The proportion of participants who either progressed as planned, successfully completed the program by obtaining a (conditional) certificate of professional competence, or transitioned to employment as care assistants
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From enrolment through programme completion (up to 36 months)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Societal business case
Time Frame: Approximately 2-3, 6 and 9 years after study start.
|
Societal business case: Conducted by Social Finance NL (SFNL), this analysis quantifies the programme's societal impact by mapping participant trajectories and expressing effects in financial terms where possible.
Outcomes are calculated over a four-year period: two years during programme participation and two years following exit.
Effects not attributable to the programme are accounted for using a zero alternative scenario, with assumptions on attribution, indexation, and discount rates applied.
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Approximately 2-3, 6 and 9 years after study start.
|
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Qualitative analysis
Time Frame: Approximately 2-3, 6 and 9 years after study start.
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A qualitative analysis to assess the impact of the programme on participants and departments.
The UMCG project coordinator invites participants to complete an anonymous survey developed jointly by Regioplan and UMCG (Appendix).
The survey contains 46 multiple-choice questions and 35 open-ended questions assessing participant experiences, satisfaction, and perceived programme effectiveness.
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Approximately 2-3, 6 and 9 years after study start.
|
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The influence of WEF-identified skills on the need for additional guidance
Time Frame: Approximately 5, 7 and 9 years after study start.
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Competencies of participants are assessed using a survey optimized during the early stages of the study.
The survey evaluates participants across multiple domains identified by the World Economic Forum (WEF) as the most in-demand skills by organizations: cognitive skills, self-efficacy, collaboration, ethics, physical skills, management skills, and technological skills.
The outcome measure assesses the relationship between participants' competency levels and the need for additional guidance or support during the programme.
An ordinal, Likert-type scale with three response options will be used.
The scale ranges from 1 to 3, with clearly defined response categories.
Data are collected systematically at predefined intervals through the REDCap system to ensure comprehensive coverage of all competency domains.
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Approximately 5, 7 and 9 years after study start.
|
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Racial microaggressions in the workplace assessed using the modified Racial Microaggressions Scale (RMAS)
Time Frame: Approximately 5-6 years and 9 years after study start.
|
This outcome measures the occurrence of potential unconscious and conscious racial microaggressions in the workplace and identifies opportunities to address and mitigate unconscious forms.
Participants complete a modified Racial Microaggressions Scale, originally developed by Torres-Harding et al. and modified by King et al.
The RMAS includes six subscales: invisibility, criminality, dysfunctional culture, sexualization, foreigner/not belonging, and environmental microaggressions.
This instrument is widely used and validated for assessing microaggressions in workplace settings.
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Approximately 5-6 years and 9 years after study start.
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Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- 22944
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
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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