- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05111327
Skills Learning and Self-confidence in Learning in High-fidelity Simulation
February 19, 2022 updated by: WONG Mei Fung Florence, Tung Wah College
Skill Learning Abilities and Students' Self-confidence in Learning in High-fidelity Simulation: A Mixed Method
High-fidelity simulation (HFS) has become a favorable innovative teaching-learning method to facilitate students' learning in professional development in nursing.
During the simulation, a variety of skills can be improved through HFS.
This mixed randomized-control and qualitative study aims to examine the effects of the structured HFS guideline on PS, CR and Student Satisfaction and Self-Confidence in Learning in undergraduate nursing students and understand their learning experience in HFS.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Nurses are facing new challenges of immediate clinical management for safer and higher quality of patient care in the current practice (Levette - Jones et al. 2018).
Students are required to have independent learning and higher-intellectual skills, including problem-solving (PS) and clinical reasoning (CR), for pursuing better clinical judgements and decision-making and the most cost-effective practice (Levette - Jones et al. 2018).
High-fidelity simulation (HFS) is one of the innovative and effective methods that allow students to apply integrated knowledge and skills in a designed simulated case scenario to develop higher-intellectual skills (Linn et al., 2012) and self-confidence.
To allow students to achieve their HFS with enhancement of skill development and self-confidence in learning, a structured guideline is useful.
This structured guideline can help course coordinators to maintain consistence in simulation teaching.
Therefore, this study aims to understand students' skill development and self- confidence in learning through the HFS.
Study Type
Interventional
Enrollment (Anticipated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: David Wong, PhD
- Phone Number: (852) 31906722
- Email: florencewong@twc.edu.hk
Study Locations
-
-
-
Kowloon, Hong Kong, 000
- Recruiting
- Florence MF Wong
-
Contact:
- Florence MF Wong, DN, MN, RN
- Phone Number: 34686838
- Email: florencewong@twc.edu.hk
-
Principal Investigator:
- Florence MF Wong, DN, MN, RN
-
-
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
No
Genders Eligible for Study
All
Description
Inclusion Criteria: Students who
- are undergraduate nursing students
- aged 18 or above
Exclusion Criteria: Students who
- are enrolled in the courses with high-fidelity simulation
- Have had clinical placement
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
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
Students in the interventional groups will receive structured simulation guideline
|
Students in the intervention group will receive more learning materials before study.
The structured guideline will be used to facilitate students' learning in simulation by the facilitator.
|
No Intervention: Control
Students in the control groups will receive standard treatment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Problem-solving skills
Time Frame: 6 months
|
Problem-solving Inventory (PSI) It consists of 32 items with a six-point Likert scale.
The PSI includes three subscales: Problem-Solving Confidence (PSC) (11 items), Approach-Avoidance Style (AAS) (16 items) and Personal Control (PC) (5 items).
PSC is to assess self-perceived confidence, belief and self-assurance effectively in solving problems.
AAS is to measure an individual's tendency of response to approach or avoid problems.
PC is to assess elements of self-control on emotions and behavior.
|
6 months
|
Nurses' Clinical Reasoning
Time Frame: 6 months
|
Nurses' Clinical Reasoning Scale (NCRS) includes 15 items with a Likert five-point scale to assess students' CR competence.
Higher scores indicate higher clinical reasoning competence.
|
6 months
|
Student Satisfaction and Self-Confidence in Learning
Time Frame: 6 months
|
The Student Satisfaction and Self-Confidence in Learning consists of 13 items with 5-likert scales to measure students' perception of their satisfaction and self-confidence in learning.
Five items are related to students' satisfaction in simulation-based learning activities and the remaining eight items concerns self-confidence in learning.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Florence MF Wong, Doctoral, Tung Wah College
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
- Cadorin L, Rei A, Dante A, Bulfone T, Viera G, Palese A. Enhancing self-directed learning among Italian nursing students: A pre- and post-intervention study. Nurse Educ Today. 2015 Jun;35(6):746-53. doi: 10.1016/j.nedt.2015.02.004. Epub 2015 Feb 18.
- Heppner, P.P. & Petersen, C.H. The development and implications of a personal problem solving inventory. Journal of Counseling Psychology. 1982; 29: 66-75.
- Linn A, Khaw C, Kildea H, Tonkin A. Clinical reasoning - a guide to improving teaching and practice. Aust Fam Physician. 2012 Jan-Feb;41(1-2):18-20.
- Liou SR, Liu HC, Tsai HM, Tsai YH, Lin YC, Chang CH, Cheng CY. The development and psychometric testing of a theory-based instrument to evaluate nurses' perception of clinical reasoning competence. J Adv Nurs. 2016 Mar;72(3):707-17. doi: 10.1111/jan.12831. Epub 2015 Oct 12.
- Levett-Jones, T. (2nd Ed.). Clinical reasoning: Learning to think like a nurse. 2018. Pearson.
- National League for Nursing. Description of available tools. 2016. Retrieved from http://www.nln.org/professional-development-programs/research/tools-andinstruments/descriptions-of-available-instruments
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)
November 1, 2021
Primary Completion (Anticipated)
June 30, 2022
Study Completion (Anticipated)
March 31, 2023
Study Registration Dates
First Submitted
October 28, 2021
First Submitted That Met QC Criteria
October 28, 2021
First Posted (Actual)
November 8, 2021
Study Record Updates
Last Update Posted (Actual)
March 8, 2022
Last Update Submitted That Met QC Criteria
February 19, 2022
Last Verified
February 1, 2022
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- REC2021102
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
There is no plan to share IPD due to confidential data.
IPD Sharing Time Frame
June to August 2022
IPD Sharing Access Criteria
Nurse educators Nurses Nurse students
IPD Sharing Supporting Information Type
- Informed Consent Form (ICF)
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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