- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05685082
Teaching the Social Determinants of Health to Nursing Students With Simulation
Teaching the Social Determinants of Health to Nursing Students With Culturally Diverse Simulation: A Quasi Experimental Trial
The goal of this intervention study is to compare two different simulation modalities (standardized patient and manikin-based) in nursing student education. The main aim is to determine the effect of new scenarios on cultural awareness levels in two different types of simulation modalities and to determine the effect of new scenarios on social determinants of health knowledge levels in two different types of simulation modalities.
Participants will assign to two groups and will attend simulation sessions.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The simulation session will contain prebriefing, simulation, and debriefing. The participants will be assigned to the simulation session.
- The first group will be the standardized patient group. They will ask to fill out the Cultural Awareness Scale and social determinants of health knowledge. Then, they will attend prebriefing, standardized patient simulation, and debriefing.
- The second group will be the manikin-based group. They will ask to fill out the Cultural Awareness Scale and social determinants of health knowledge. Then, they will attend prebriefing, manikin-based simulation, and debriefing.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02125
- University of Massachusetts Boston
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- being enrolled in Nursing in the Community course
- accepting to be a participant
- accepting to be recorded
Exclusion Criteria:
- not attending at least one of the prebriefing, simulation, or debriefing sessions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Standardized patient group
The standardized patient simulation participants will receive a simulation with standardized patients on how to identify social determinants of health in an individual
|
The standardized patient simulation participants will receive a simulation with standardized patients on how to identify social determinants of health in an individual
|
Experimental: Manikin-based group
The manikin-based simulation participants will receive a simulation with manikins on how to identify social determinants of health in an individual
|
The manikin-based simulation participants will receive a simulation with manikins on how to identify social determinants of health in an individual
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline cultural awareness level on the 36 questions Cultural Awareness Scale
Time Frame: Three hour
|
The Cultural Awareness Scale is a validated, reliable, and self-reported instrument assessing cultural awareness levels.
Each statement is graded from 1=Strongly Disagree to 7=Strongly Agree.
While lower scores indicate less cultural awareness, higher scores indicate greater cultural awareness (minimum = 36, maximum = 252).
|
Three hour
|
Change from baseline social determinants knowledge on the 10 questions Social Determinants of Health Survey
Time Frame: Three hour
|
Social Determinants of Health Survey is a 10-question multiple-choice survey created by researchers by searching the literature.
The number of responses to the answer choice is determined.
The lower scores indicate fewer social determinants of health knowledge and higher scores indicate greater social determinants of health knowledge (minimum = 0, maximum = 10).
|
Three hour
|
Collaborators and Investigators
Investigators
- Principal Investigator: Semiha Asli Bozkurt, PhD, University of Massachusetts, Boston
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- BOZKURT-Int-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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