- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05945316
Performance Improvement: Does Mock Code Simulation Improve the Confidence Level of Newly Graduated Nurses?
July 23, 2025 updated by: Methodist Health System
The study is a descriptive correlational study over three surveys that will examine the improvement of confidence level associated between the implementation of mock code training simulation and the real live event.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Participants will be asked to respond online to a questionnaire or survey launched via Survey Monkey®.
Demographic information will be collected first Appendix B. A self-reported confidence level via the Student Satisfaction and self-confidence in learning scale will be utilized and serves as a data collection tool.
The scale will be deployed via email as a scale A B and C Appendix C to each study participant and is the same scale.
The participants will complete survey A after completion of the initial educational simulation training the survey B will be completed when the participants attended an unannounced simulation activity.
Survey C will be completed after the first actively involved Code Blue situation.
The survey is a 13-item instrument designed to measure student satisfaction five items with the simulation activity and self-confidence in learning eight items using a five-point scale.
Reliability was tested using Cronbach's alpha: satisfaction equals 0.94 self-confidence equals 0.87 Franklin Burns and Lee 2014.
Study Type
Observational
Enrollment (Actual)
150
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
-
-
Texas
-
Dallas, Texas, United States, 75203
- Methodist Dallas Medical Center
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
All newly graduated nurses and nurse fellows in a residency training program at MCMC Able to read and understand English
Description
Inclusion Criteria:
All newly graduated nurses and nurse fellows in a residency training program at MCMC Able to read and understand English
Exclusion Criteria:
Clinical staff not affiliated with the residency and fellowship program.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accessing Confidence levels of Nursing students during CODE BLUE
Time Frame: 2 years
|
The confidence level will be measured utilizing the Student Satisfaction and Self-Confidence in Learning Scale (SCLS).
SCLS is a 13-item survey instrument designed to measure student satisfaction (five items) with the simulation activity and self-confidence in learning (eight items).
Statements will be confirmed with answers on a five-point Likert scale: strongly disagree (1), disagree (2), undecided (3), agree (4), and strongly agree (5).
Measures will occur during three different activities.
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Simulated cardiopulmonary resuscitation will improve confidence level in newly graduated nurses and nurse fellows during their residency training
Time Frame: 2 yrs
|
The confidence level will be measured utilizing the Student Satisfaction and Self Confidence in Learning Scale (SCLS).
SCLS is a 13-item survey instrument designed to measure student satisfaction (five items) with the simulation activity and self-confidence in learning (eight items).
Statements will be confirmed with answers on a five-point Likert scale: strongly disagree (1), disagree (2), undecided (3), agree (4), and strongly agree (5).
Measures will occur during three different activities.
|
2 yrs
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Anne-Gret Friedrich-Cuntz, EdD, Methodist Charlton Medical Center (Methodist Health System-
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Advice, P.R.N. (2004). Staff development: Mock code, real value. Nursing2004
- Carroll L, Pignataro S. Use of portable simulation manikins to increase the frequency of mock code training on four inpatient surgical units. J Contin Educ Nurs. 2009 Jun;40(6):250-1. doi: 10.3928/00220124-20090522-04.
- Carney P. Mock code: a game that saves lives. RN (For Managers). 1983 Jul;46(7):18P. No abstract available.
- Cardoza MP, Hood PA. Comparative study of baccalaureate nursing student self-efficacy before and after simulation. Comput Inform Nurs. 2012 Mar;30(3):142-7. doi: 10.1097/NCN.0b013e3182388936.
- Franklin AE, Burns P, Lee CS. Psychometric testing on the NLN Student Satisfaction and Self-Confidence in Learning, Simulation Design Scale, and Educational Practices Questionnaire using a sample of pre-licensure novice nurses. Nurse Educ Today. 2014 Oct;34(10):1298-304. doi: 10.1016/j.nedt.2014.06.011. Epub 2014 Jul 9.
- Hill CR, Dickter L, Van Daalen EM. A matter of life and death: the implementation of a Mock Code Blue Program in acute care. Medsurg Nurs. 2010 Sep-Oct;19(5):300-2, 304. No abstract available.
- Huseman KF. Improving code blue response through the use of simulation. J Nurses Staff Dev. 2012 May-Jun;28(3):120-4. doi: 10.1097/NND.0b013e3182551506.
- Kakora-Shiner N. Using ward-based simulation in cardiopulmonary training. Nurs Stand. 2009 May 27-Jun 2;23(38):42-7. doi: 10.7748/ns2009.05.23.38.42.c6975.
- Marsch SC, Muller C, Marquardt K, Conrad G, Tschan F, Hunziker PR. Human factors affect the quality of cardiopulmonary resuscitation in simulated cardiac arrests. Resuscitation. 2004 Jan;60(1):51-6. doi: 10.1016/j.resuscitation.2003.08.004.
- Ngo DQ, Vu C, Nguyen T, Sotolongo P, Talati M, Zahabi N, Platt K. The Effect of Mock Code Blue Simulations and Dedicated Advanced Cardiac Life Support Didactics on Resident Perceived Competency. Cureus. 2020 Nov 25;12(11):e11705. doi: 10.7759/cureus.11705.
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)
March 16, 2022
Primary Completion (Actual)
July 22, 2025
Study Completion (Actual)
July 22, 2025
Study Registration Dates
First Submitted
July 6, 2023
First Submitted That Met QC Criteria
July 6, 2023
First Posted (Actual)
July 14, 2023
Study Record Updates
Last Update Posted (Actual)
July 25, 2025
Last Update Submitted That Met QC Criteria
July 23, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 008.NUR.2022.C
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The PI is committed to disseminate research results in a timely fashion.
Sharing of results generated by the data analysis during the course of the project will be through presentation at national scientific meetings and/or publication in open access journals.
All information obtained will be source de-identified and presented on a large scale and not traceable to any one particular individual.
IPD Sharing Time Frame
Data will become available with in 1 to 2 years.
All study-related documents will be retained by the CRI until at least three years after study completion or according to local laws, whichever is longer. .
Records will also be accessible to MHS staff upon request unless constituting a violation of patient confidentiality.
IPD Sharing Access Criteria
All study-related documents will be retained by the CRI until at least three years after study completion or according to local laws, whichever is longer. .
Records will also be accessible to MHS staff upon request unless constituting a violation of patient confidentiality.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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