- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05276427
Impact of External Factors(Brexit and Covid-19) on Retention and Turnover in the NHS
April 22, 2026 updated by: NHS Grampian
The Impact of External Factors (Brexit and Covid 19) on Retention and Turnover Among Nurses and Consultants in NHS Grampian
Problems with retention and staff turnover in the health sectors of many western countries have a long history and have thus attracted research attention over the years.
The National Health Service (NHS) in the United Kingdom (UK) is not immune to this problem as it is reported that the NHS as an organisation is struggling to meet staffing demands particularly with its nursing and medical workforce.
One of the ways to tackle this problem has been to recruit staffs from European union countries.
With the exit of UK from the EU, there are concerns on the this departure on staffing.
While the UK was still coming to terms with BREXIT and its effect on the NHS, the current COVID 19 pandemic struck and has intensified workload and demands on the health sector, particularly the NHS.
As a result of this, many NHS employees believe more should be done to show they are valued and appreciated for all their hard work.
Turnover is already high among clinical occupations in the NHS as people leave for various reasons.
It is therefore important to study the combined effect of these external factors (BREXIT and COVID 19) on turnover and retention in the NHS Grampian.
It is hoped that this study will be beneficial to NHS Grampian management and policy makers as it will aid early identification of intention to leave and possibly enhance staff retention.
The study will be carried out in Scotland and will be limited to NHS Grampian.
Nurses and consultants who have been in employed in NHS Grampian prior to BREXIT and COVID 19 will be invited participate.
Participants will voluntarily take part in a semi structured interview which may last for about 45 to 60 minutes.
The project is self-funded for the award of a PhD in management studies.
Study Overview
Study Type
Observational
Enrollment (Actual)
30
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
-
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Aberdeen, United Kingdom
- Research and governance team
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Nurses who have been trained in different aspects of nursing such as paediatric, neonatal, critical care, surgical, emergency care etc and consultants who have specialist training in specific aspect of medicine who have had to deal with the impact and pressures of COVID 19 and BREXIT will be invited to participate in the study.
Description
Inclusion Criteria:
- Must be employed in NHS Grampian prior to January 2020.
- Must be a Nurse or Consultant
Exclusion Criteria:
- Limited to Nurses and Consultants.
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Non clinical procedure
Completion of consent form and interview session
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Non clinical procedure- Informed consent completion and interview session
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Participants will be interviewed to assess the impact of external factors on retention and turnover.
Time Frame: 45- 60 minutes
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45- 60 minutes
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Interviews with 40 participants will be analysed using NVivo qualitative software.
Time Frame: 45-60minutes
|
45-60minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Donald Hislop, University of Aberdeen
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)
April 5, 2022
Primary Completion (Actual)
May 31, 2025
Study Completion (Actual)
May 31, 2025
Study Registration Dates
First Submitted
February 8, 2022
First Submitted That Met QC Criteria
March 10, 2022
First Posted (Actual)
March 11, 2022
Study Record Updates
Last Update Posted (Actual)
April 28, 2026
Last Update Submitted That Met QC Criteria
April 22, 2026
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2-083-21
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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