- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06712953
The Effect of Repeated Standardized Patient Use on Students' Anxiety and Learning Levels in Teaching Extremity Examination Skills
Aims: This study aimed to examine the effects of peer assessment and repeated standardized patient use on students' self-confidence and anxiety and their psychomotor skill performance in teaching extremity examination skills.
Design: This randomized controlled experimental study was carried out following the CONSORT checklist.
Methods: The study sample consisted of second-grade nursing students enrolled in the " Health Diagnosis" course in the fall semester of the 2023-2024 academic year (n:67). The students in the peer assessment group performed the upper and lower extremity examinations once whereas those in the standardized patient group performed these examinations three times. Research data were analyzed in IBM SPSS 25.0 (Statistical Package for Social Sciences) software. The Shapiro-Wilk test was used to check whether the data were normally distributed. Parametric and nonparametric tests and descriptive statistical methods were used for data analysis. The significance levels were taken as p<0.001 and p<0.05. The scales used were analyzed with the Cronbach alpha reliability coefficient; the scenarios and forms created by the researchers were evaluated with the Lawshe Technique.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Center
-
Isparta, Center, Turkey, 32260
- Suleyman Demirel University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Second-grade nursing students
- Enrolled in the " Health Diagnosis" course at the Faculty of Health Sciences, Department of Nursing of a university in the fall semester of the 2023-2024 academic year
Exclusion Criteria:
- Students who actively continue their nursing profession as well as their education life
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: the peer assessment group
Students in the peer assessment group were paired (by randomization, on their request) to have a teammate of the same sex before the extremity examination experience.
In the following process, the students were asked to perform extremity examinations in line with the specified objectives.
|
Students in the peer assessment group were paired (by randomization, on their request) to have a teammate of the same sex before the extremity examination experience.
In the following process, the students were asked to perform extremity examinations in line with the specified objectives.
Students in the standardized patient group were asked to perform extremity examinations per the specified objectives in standardized patient.
|
|
Experimental: the standardized patient group
Students in the standardized patient group were asked to perform extremity examinations per the specified objectives in standardized patient.
|
Students in the peer assessment group were paired (by randomization, on their request) to have a teammate of the same sex before the extremity examination experience.
In the following process, the students were asked to perform extremity examinations in line with the specified objectives.
Students in the standardized patient group were asked to perform extremity examinations per the specified objectives in standardized patient.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Extremity examinations
Time Frame: First week
|
The students in the standardized patient group performed extremity examinations on the same standardized patient three times, whereas the students in the peer assessment group performed this examination on their peers once
|
First week
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
First measurement (Self-conficent and Anxiety)
Time Frame: First week
|
The students in the standardized patient group performed extremity examinations on the same standardized patient three times, whereas the students in the peer assessment group performed this examination on their peers once.
|
First week
|
|
Second measurement (Self-conficent and Anxiety)
Time Frame: Third week
|
The students in the standardized patient group performed extremity examinations on the same standardized patient three times, whereas the students in the peer assessment group performed this examination on their peers once
|
Third week
|
|
Third measurement (Self-conficent and Anxiety)
Time Frame: fifth week
|
The students in the standardized patient group performed extremity examinations on the same standardized patient three times, whereas the students in the peer assessment group performed this examination on their peers once
|
fifth week
|
Collaborators and Investigators
Sponsor
Publications and helpful links
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 72867572-050.01.04-616349
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
product manufactured in and exported from the U.S.
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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