- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05941026
Developing Nursing Students' Intercultural Sensitivity Levels
Developing Nursing Students' Intercultural Sensitivity Levels: A Randomized Controlled Experimental Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Cultural sensitivity is extremely important for healthcare professionals. Understanding cultural differences can help build a trusting relationship between patients and healthcare professionals. This increases patient satisfaction and improves the quality of health services.
This work; This is a randomized controlled experimental type study designed to improve the intercultural sensitivity levels of nursing students.
Intercultural sensitivity training does not affect the intercultural sensitivity level of nursing students.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Aydın, Turkey
- Aydın Adnan Menderes University Institute of Health Sciences Department of Public Health Nursing
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a student of Aydın Adnan Menderes University Nursing Department
- Having successfully completed the basic practical courses of the first three classes
- Being enrolled in one of the Public Health Nursing or Mental Health and Diseases Nursing courses from the fourth year
- Volunteer to participate in the study
Exclusion Criteria:
• Not completing the training sessions of the research
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Arms
Nursing students who were in the experimental group during the application phase of the study were given training to develop their intercultural sensitivity levels based on Leninger's Intercultural Nursing Theory.
Data were collected at the beginning of the four-week online training, at the end of the training, and one month after the training.
|
The educational content of the research was created by the researcher in line with the literature and expert opinions and covers the following topics. Educational subjects
The training is an online training and continued via video conference, and a session invitation was sent to the participants before each session. In addition, after the training, brochures containing the training topics of each week were prepared and delivered to the participants. The trainings were conducted by the researcher in a total of four sessions (each session 20 minutes) once a week during the training process. During the training, the questions of the participants were answered. |
No Intervention: Control groups
No application was made to the control group within the scope of the research.
Data were collected simultaneously with only the experimental group.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Intercultural Sensitivity Scale and Personel Questions
Time Frame: Pre-test (Before the training)
|
The scale was developed by Chen and Starosta and was adapted to Turkish in 2010.
It consists of twenty-four items and includes five emotional dimensions necessary to measure intercultural sensitivity.
The scale has five dimensions: responsibility in communication, respect for cultural differences, self-confidence in communication, enjoying communication, and being careful in communication.
The scale has a 5-point Likert-type rating.
As the score obtained from the scale increases, the level of sensitivity increases.
The Cronbach's alpha value of the scale was determined as 0.90.
|
Pre-test (Before the training)
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Intercultural Sensitivity Scale
Time Frame: four weeks after the pre-test (at the end of the training)
|
The scale was developed by Chen and Starosta and was adapted to Turkish in 2010.
It consists of twenty-four items and includes five emotional dimensions necessary to measure intercultural sensitivity.
The scale has five dimensions: responsibility in communication, respect for cultural differences, self-confidence in communication, enjoying communication, and being careful in communication.
The scale has a 5-point Likert-type rating.
As the score obtained from the scale increases, the level of sensitivity increases.
The Cronbach's alpha value of the scale was determined as 0.90.
|
four weeks after the pre-test (at the end of the training)
|
Intercultural Sensitivity Scale
Time Frame: eight weeks after the pre-test (and one month after the training)
|
The scale was developed by Chen and Starosta and was adapted to Turkish in 2010.
It consists of twenty-four items and includes five emotional dimensions necessary to measure intercultural sensitivity.
The scale has five dimensions: responsibility in communication, respect for cultural differences, self-confidence in communication, enjoying communication, and being careful in communication.
The scale has a 5-point Likert-type rating.
As the score obtained from the scale increases, the level of sensitivity increases.
The Cronbach's alpha value of the scale was determined as 0.90.
|
eight weeks after the pre-test (and one month after the training)
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Öner ALTINTOP, MsC, Aydın Adnan Menderes University Institute of Health Sciences Department of Public Health Nursing
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Intercultural Sensitivity
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- CSR
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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