- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05943639
Effect of Cultural Marginality Theory-Based Education on Intercultural Adaptation and Psychological Well-Being of Foreign Nursing Students
December 27, 2024 updated by: Hilal Altundal
The Effect of Cultural Marginality Theory-Based Education on Intercultural Adaptation and Psychological Well-Being of Foreign Nursing Students: A Randomized Controlled Study
In this study, between 1 - 31 December 2022, who met the inclusion and exclusion criteria, a total of 66 foreign nursing students who are with 1st year foreign students starting the Nursing Department of Ondokuz Mayıs University and Mersin University.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
The Cultural Marginality Theory-Based Education program will be held in a face-to-face classroom environment for the students in the experimental group.
This training program has been developed based on the concepts of Cultural Marginality Theory.
The content and topics of the sessions in the program are arranged according to the conceptual structure and flow of the theory.
The training program was created in a certain flow, based on the concepts of recognizing intercultural conflict (2 sessions), marginal living (2 sessions) and alleviating cultural tension (2 sessions).
There are 6 sessions in the program and the frequency of sessions is 2 times a week, and each session lasts approximately 45 minutes.
The training program will be applied to 33 foreign nursing students in the experimental group.
In the first session to the students in the experimental group and to the students in the control group after the post-tests, the training booklet, which consists of information about the educational content in the program, will be given online in pdf format in color and with pictures.
Study Type
Interventional
Enrollment (Actual)
66
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
-
-
-
Çankırı, Turkey, 18100
- Hilal ALTUNDAL DURU
-
-
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 first-year foreign nursing student studying at state universities in the north and south two cities of Türkiye,
- agreeing to participate in the research
- not having communication barrier
Exclusion Criteria:
1) having a physical or mental illness that would prevent participation in the research
The Termination Criteria:
- withdrawing from the research voluntarily
- not attending at least one of the sessions
- incomplete or incorrectly answering the instruments
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
The Cultural Marginality Theory-Based Education program will be held in a face-to-face classroom environment for the students in the experimental group.
This training program has been developed based on the concepts of Cultural Marginality Theory.
The content and topics of the sessions in the program are arranged according to the conceptual structure and flow of the theory.
The training program was created in a certain flow, based on the concepts of recognizing intercultural conflict (2 sessions), marginal living (2 sessions) and alleviating cultural tension (2 sessions).
There are 6 sessions in the program and the frequency of sessions is 2 times a week, and each session lasts approximately 45 minutes.
The training program will be applied to 33 foreign nursing students in the experimental group.
|
The Cultural Marginality Theory-Based Education program will be held in a face-to-face classroom environment for the students in the experimental group.
This training program has been developed based on the concepts of Cultural Marginality Theory.
The content and topics of the sessions in the program are arranged according to the conceptual structure and flow of the theory.
The training program was created in a certain flow, based on the concepts of recognizing intercultural conflict (2 sessions), marginal living (2 sessions) and alleviating cultural tension (2 sessions).
There are 6 sessions in the program and the frequency of sessions is 2 times a week, and each session lasts approximately 45 minutes.
The training program will be applied to 33 foreign nursing students in the experimental group.
|
|
No Intervention: Control group
There will be no training or intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
CROSS CULTURAL ADAPTABILITY INVENTORY (CCAI)
Time Frame: Change from before education up to after education (three weeks)
|
The Turkish adaptation of the inventory developed by Kelley and Meyers in 1992 was made in 2009 by Karaeminoğulları, Doğan and Bozkurt.
The Intercultural Adaptation Inventory consists of 49 items and is 6-point Likert type.
A high score from the inventory indicates cultural compatibility, and a low score indicates incompatibility with the culture.
The inventory assesses individuals' levels of intercultural activity and their abilities regarding individual awareness against the characteristics of the culture they live in.
These dimensions are emotional flexibility (18 items), flexibility/openness (15 items), perceptual sensitivity (10 items), and personal autonomy (7 items).
The Cronbach alpha internal consistency coefficient of the Intercultural Adaptation Inventory is 0.84.
|
Change from before education up to after education (three weeks)
|
|
THE PSYCHOLOGICAL WELL-BEING SCALE (PWS)
Time Frame: Change from before education up to after education (three weeks)
|
The scale developed by Diener et al. (2010) was developed to measure socio-psychological well-being, complementing existing well-being measures.
The Turkish adaptation of the scale was carried out by Telef in 2013.
The Single Factor Psychological Well-Being Scale consists of 8 items and is in 7-point Likert type.
All items are expressed positively.
Scores from the scale range from 8 to 56.
The higher the score obtained from the scale, the higher the level of psychological well-being is calculated.
The Cronbach alpha internal consistency coefficient of the scale is 0.80.
|
Change from before education up to after education (three weeks)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Hilal ALTUNDAL DURU, Doctor, Çankırı Karatekin 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 (Actual)
September 15, 2022
Primary Completion (Actual)
January 17, 2023
Study Completion (Actual)
September 15, 2024
Study Registration Dates
First Submitted
June 26, 2023
First Submitted That Met QC Criteria
July 5, 2023
First Posted (Actual)
July 13, 2023
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 27, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ÇankırıKaratekinU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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