- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02100215
Quantifying the Influence of Expert Modeling
April 30, 2019 updated by: Ashley Franklin, Oregon Health and Science University
Quantifying the Influence of Expert Modeling on Novice Nurse Competence and Self-Efficacy
The purpose of this study is to learn more about the effects of various types of simulation preparation methods on novice nurses' competence and self-efficacy.
Participants will be recruited from an academic course (N424 Integrated Practicum).
Participants will be randomized to three intervention groups (i.e.
expert modeling video, voice over PowerPoint, and traditional readings).
All participants will complete self-efficacy surveys and two simulations.
During simulation, participants will be scored based on their competence according to a performance rubric.
The hypothesis is that participants in the expert modeling group will demonstrate more change in competence and report more change in self-efficacy scores than participants in other groups.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Investigators will compare self-confidence and competence scores between the three groups after the pre-test and posttest simulations.
The self-efficacy survey is an 7-item scale that involves participants rating their self-efficacy about providing care for multiple patients.
Participants rate their self-efficacy on a 1 to 5 (not confident to very confident scale).
The survey takes 5 minutes to complete.
The self-efficacy survey has been used in many simulation research studies previously with novice nurses.
Competence will be measured with a rater-observation measure which has previously been used in simulation research.
Study Type
Interventional
Enrollment (Actual)
20
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 Locations
-
-
Oregon
-
Ashland, Oregon, United States, 97520
- Oregon Health & Science University, School of Nursing
-
-
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 to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Enrolled in capstone clinical course
- Oregon Consortium for Nursing Education curriculum
- Ashland, OR
Exclusion Criteria:
- No exclusion criteria
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: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Expert Modeling
Participants will have access to 70 minutes of expert modeling videos available over 5 weeks on an online learning management system.
The investigator will be the expert model in the videos.
Expert modeling videos will address content related to seven concepts: Taking report with a graphic organizer worksheet, prioritizing patient care, delegating to unlicensed assistive personnel, safety checks in patient rooms, focused physical assessments, safe medication administration, and using a standardized healthcare provider communication tool on the telephone.
|
Participants in all groups have common readings related to policies for nursing care in acute care facilities.
There will be additional handouts related to performing safety checks and a focused physical assessment.
70 minutes of expert modeling videos
|
Active Comparator: Voice Over PowerPoint
Participants will have access to 60 minutes of voice over PowerPoint slides, available over 5 weeks on an online learning management system, specifically to match exposure and content with the expert modeling video group.
The script for PowerPoint will contain content related to the aforementioned seven concepts.
There will be static photos, but no expert modeling videos, on PowerPoint slides.
The investigator will narrate the voice over PowerPoint.
|
Participants in all groups have common readings related to policies for nursing care in acute care facilities.
There will be additional handouts related to performing safety checks and a focused physical assessment.
60 minutes of Voice Over PowerPoint presentations
|
Placebo Comparator: Reading
Participants will have access to articles, policies, and procedures on an online learning management system.
The estimated time required for participants to review these materials is 45 minutes
|
Participants in all groups have common readings related to policies for nursing care in acute care facilities.
There will be additional handouts related to performing safety checks and a focused physical assessment.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Creighton Simulation Evaluation Instrument
Time Frame: Change from baseline on Creighton Simulation Evaluation Instrument at 5 weeks
|
Change from baseline on Creighton Simulation Evaluation Instrument at 5 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
National League for Nursing Student Satisfaction and Self-Confidence with Learning scale
Time Frame: Change from baseline on NLN Student Satisfaction and Self-Confidence with Learning scale at 5 weeks
|
Change from baseline on NLN Student Satisfaction and Self-Confidence with Learning scale at 5 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ashley Franklin, Oregon Health and Science University
- Study Chair: Christopher S Lee, PhD, Oregon Health and Science University
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
November 1, 2013
Primary Completion (Actual)
June 1, 2014
Study Completion (Actual)
June 1, 2014
Study Registration Dates
First Submitted
March 24, 2014
First Submitted That Met QC Criteria
March 26, 2014
First Posted (Estimate)
March 31, 2014
Study Record Updates
Last Update Posted (Actual)
May 2, 2019
Last Update Submitted That Met QC Criteria
April 30, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MPtSim-Ashland
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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