- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05269277
Health System Methods to Improve Nursing Retention Amidst Ongoing COVID-19 Pandemic: a Mixed Method Study
June 6, 2025 updated by: Claire Aksamit, Poudre Valley Health System
This study is a mixed-method exploratory study with the aim to determine an objective compensation or mechanism of support from a healthcare system standpoint to aid in retention of nursing staff amidst the ongoing COVID-19 pandemic.
It will include semi-structured qualitative interviews of current and prior nursing staff from the Trauma/Surgical floor, Progressive Care Unit, and ICU, in addition to Trauma/Surgical unit and system administrators; the second portion of the study will include a quantitative survey distributed via email to current nurses on the Trauma/Surgical floor, Progressive Care Unit, and ICU to assess ranked priority of additional mechanisms of support to improve intention of retention.
Study Overview
Status
Enrolling by invitation
Study Type
Observational
Enrollment (Estimated)
120
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
-
-
Colorado
-
Loveland, Colorado, United States, 80538
- UCHealth - Medical Center of the Rockies
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Participants for the qualitative interviews will include current bedside nursing and clinical administrative staff at UCHealth - Medical Center of the Rockies on the Trauma/Surgical floor, the Surgical Progressive Care Unit, and the Surgical ICU.
Other participants will also include prior nurses who have left their job on these respective units in the prior 24 months.
Registered nurses, men and women, day-time and night-time nurses, full-time versus part-time nurses, and those with variable lengths of experience will be incorporated who have been or are currently involved with direct patient care during the COVID-19 pandemic.
The quantitative survey will be distributed to all current nurses on the above listed units.
Description
Inclusion Criteria:
- Registered nurses on the Trauma/Surgical floor, Surgical Progressive Care Unit, or Surgical ICU who are currently working or who have worked bedside in the past 24 months
- Adult hospital administrative staff
Exclusion Criteria:
- Non-Registered nurses (ie. CNAs, LPNs)
- RNs without clinical bedside experience in the past 24 months
- RNs working on other units beside the Trauma/Surgical floor, Surgical Progressive Care Unit, or Surgical ICU
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: Cohort
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Identify a common mechanism or implementation to improve intention of retention or nurses amongst the Trauma/Surgical units amidst COVID-19
Time Frame: 24 months
|
The goal is to identify a common theme amongst nurses on the Trauma/Surgical units regarding a means of compensation or action item from the healthcare system to improve intention of retention amidst ongoing COVID-19 pandemic.
Obtaining this is two-fold, to include qualitative interviewing with nurses on the affected units first-hand with subsequent transcription and coding to identify common themes; and a widely distributed quantitative survey to assess ranked priorities to implement to improve intention of retention.
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Commonly-identified challenges nurses are facing on a Trauma/Surgical unit during COVID-19
Time Frame: 24 months
|
The goal is to identify common challenges nurses on Trauma/Surgical units during COVID-19.
This will primarily be obtained via qualitative interviewing of nurses on the affected unit first-hand to discuss the most challenging parts of their jobs, in particularly during COVID-19, subsequently followed by transcription and coding and analysis to identify common themes.
|
24 months
|
|
Commonly-identified support mechanisms implemented by the healthcare system that have aided in intention of retention of nurses on a Trauma/Surgical unit during COVID-19
Time Frame: 24 months
|
The goal is to identify common interventions the healthcare systems has provided that has helped with intention of retention of nursing staff during COVID-19.
To obtain this, qualitative interviewing will be done speaking to affected nurses first-hand, following by subsequent transcription and coding and data analysis to identify these common themes.
|
24 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Claire Aksamit, University of Colorado Health
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)
February 23, 2022
Primary Completion (Estimated)
December 31, 2025
Study Completion (Estimated)
December 31, 2025
Study Registration Dates
First Submitted
March 1, 2022
First Submitted That Met QC Criteria
March 4, 2022
First Posted (Actual)
March 7, 2022
Study Record Updates
Last Update Posted (Actual)
June 8, 2025
Last Update Submitted That Met QC Criteria
June 6, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 21-4768
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.
Clinical Trials on Motivational Factors for Nurse Retention
-
National University of SingaporeTan Tock Seng HospitalCompletedWeb-based Program for Nurse PreceptorsSingapore
-
San Diego State UniversityUniversity of IbadanCompletedRisk Factors for Intimate Partner ViolenceNigeria
-
University of MiamiNot yet recruitingExercise Training | Motivation for Physical Activity | Motivational Enhancement | Exercise Behavior | Exercise Adherence ChallengesUnited States
-
University of RostockCompletedPatient and Surgical Related Risk Factors for Complications
-
University GhentCompletedRisk Factors for Shoulder InjuriesNetherlands
-
Universitaire Ziekenhuizen KU LeuvenCompletedPrevalence of Augmented Renal Clearance | Risk Factors for Augmented Renal ClearanceBelgium
-
Prince of Songkla UniversityNot yet recruitingRisk Factors for Post ACL Reconstruction Pain
-
University of MilanActive, not recruitingParticipants With/Without Risk Factors for Metabolic DiseasesItaly
-
Ningbo No. 1 HospitalCompletedIdentification of Influencing Factors and Construction of a Prediction Model for New-Onset Diabetes After PancreatectomyChina
-
A.G. HuppelschotenUnknownQuality of Life | Patient Centredness | Risk Factors for Emotional MaladjustmentNetherlands