Developing Nursing Students' Intercultural Sensitivity Levels

July 10, 2023 updated by: ÖNER ALTINTOP, Aydin Adnan Menderes University

Developing Nursing Students' Intercultural Sensitivity Levels: A Randomized Controlled Experimental Study

This study; This is a randomized controlled experimental type study designed to improve the intercultural sensitivity levels of nursing students.

Study Overview

Status

Completed

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

Interventional

Enrollment (Actual)

117

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

      • Aydın, Turkey
        • Aydın Adnan Menderes University Institute of Health Sciences Department of Public Health 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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

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

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: 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

  1. Culture and Concepts Related to Culture
  2. Culture/Cultural Characteristics and Cultural Elements in Terms of Social Structure
  3. Cultural Factors Affecting Health and Disease
  4. Concepts and Practices Related to the Field of Study

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.

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)
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

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Öner ALTINTOP, MsC, Aydın Adnan Menderes University Institute of Health Sciences Department of Public Health Nursing

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)

June 1, 2021

Primary Completion (Actual)

October 1, 2022

Study Completion (Actual)

April 1, 2023

Study Registration Dates

First Submitted

June 21, 2023

First Submitted That Met QC Criteria

July 10, 2023

First Posted (Actual)

July 12, 2023

Study Record Updates

Last Update Posted (Actual)

July 12, 2023

Last Update Submitted That Met QC Criteria

July 10, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Intercultural Sensitivity

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The data sets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request

IPD Sharing Time Frame

6 months after publication

IPD Sharing Access Criteria

relevance to the topic of the study and approval of all co-authors within 1 month of receiving the request.

IPD Sharing Supporting Information Type

  • CSR

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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