- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05993403
The Cultural Sensitivity Education Program
July 4, 2024 updated by: Sultan Ayaz Alkaya
The Effect of The Cultural Sensitivity Education Program Applied to Nurses on The Level of Intercultural Sensitivity and Compassion
The research was carried out with a randomized controlled experimental design in order to determine the effect of intercultural sensitivity training applied to nurses on intercultural sensitivity and compassion level.
Nurses working in a private hospital were included in the sample of the study.
A total of 66 nurses, 32 of whom were in the intervention and control groups, were included in the study.
"Personal Information Form", "Intercultural Sensitivity Scale" and "Compassion Scale" were used to collect data.
"Intercultural Sensitivity Training" consisting of four sessions was given to the intervention group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Within the scope of the research, an intercultural sensitivity training program for nurses was created.
The training program was implemented and an evaluation was made after the implementation.
Study Type
Interventional
Enrollment (Actual)
64
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
-
-
-
Ankara, Turkey
- Gazi University
-
-
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 nurse working under the Nursing Services Directorate
- Volunteering to participate in research
Exclusion Criteria:
- Having a disease that prevents participation in the study
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intercultural Sensitivity Education
Data collection tools were applied to this group before the research.
A training program consisting of three sessions was applied to the intervention group.
Each training session lasted an average of 90-100 minutes.
Various methods and techniques were used in the trainings.
|
The training program consists of three sessions.
In the Intercultural Sensitivity training for nurses, it was aimed to develop the level of intercultural sensitivity, and it was aimed to provide proficiency in providing services to raise awareness and knowledge about intercultural sensitivity.
|
|
No Intervention: Control
Data collection tools were applied to this group before the research.
No intervention was applied to this group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intercultural Sensitivity Level (Intercultural Sensitivity Scale)
Time Frame: before the implementation
|
The Intercultural Sensitivity scale is a five-point Likert type and consists of 24 items.
The lowest total score that can be obtained from the scale was calculated as 24 and the highest score as 120.
An increase in the score obtained from the scale indicates an increase in the level of intercultural sensitivity.
|
before the implementation
|
|
Intercultural Sensitivity Level (Intercultural Sensitivity Scale)
Time Frame: four weeks after the start of application
|
The Intercultural Sensitivity scale is a five-point Likert type and consists of 24 items.
The lowest total score that can be obtained from the scale was calculated as 24 and the highest score as 120.
An increase in the score obtained from the scale indicates an increase in the level of intercultural sensitivity.
|
four weeks after the start of application
|
|
Intercultural Sensitivity Level (Intercultural Sensitivity Scale)
Time Frame: three months after the finish of implementation
|
The Intercultural Sensitivity scale is a five-point Likert type and consists of 24 items.
The lowest total score that can be obtained from the scale was calculated as 24 and the highest score as 120.
An increase in the score obtained from the scale indicates an increase in the level of intercultural sensitivity.
|
three months after the finish of implementation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 1, 2023
Primary Completion (Actual)
June 15, 2023
Study Completion (Actual)
October 21, 2023
Study Registration Dates
First Submitted
August 8, 2023
First Submitted That Met QC Criteria
August 14, 2023
First Posted (Actual)
August 15, 2023
Study Record Updates
Last Update Posted (Actual)
July 8, 2024
Last Update Submitted That Met QC Criteria
July 4, 2024
Last Verified
August 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023-558520
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.
Clinical Trials on Intercultural Sensitivity
-
University of Turin, ItalyCompletedGluten Sensitivity | Wheat SensitivityItaly
-
Universidade Federal do ParaCompletedColor | Bleaching SensitivityBrazil
-
University of New EnglandUniversity of IowaCompletedTooth Discoloration | Teeth SensitivityUnited States
-
Universidad Peruana Cayetano HerediaUniversity of WashingtonUnknownDental Sensitivity | Gingival ConditionPeru
-
Cairo UniversityNot yet recruitingComparative Efficacy of Laser Systems and Fluoride in Managing Dentinal Hypersensitivity: RCT (DHLT)Dentin Sensitivity, Dentine Hypersensitivity, Tooth Sensitivity
-
Faculty of Dental Medicine for GirlsAl-Azhar UniversityCompletedTeeth Sensitivity | Treated Dentin SurfacesEgypt
-
Colgate PalmoliveCompleted
-
University of PalermoCompletedNon-celiac Wheat Sensitivity | Non-celiac Gluten SensitivityItaly
-
Lacer S.A.Completed
-
Universidade Federal FluminenseActive, not recruitingTooth SensitivityBrazil
Clinical Trials on Intercultural Sensitivity Education Program
-
Giresun UniversityCompletedHealth Knowledge, Attitudes, Practice | Cultural CompetencyTurkey (Türkiye)
-
University of VermontNational Institute on Drug Abuse (NIDA)Completed
-
Florida State UniversityCompletedExperimental | Placebo ContolUnited States
-
Florida State UniversityCompletedComputerized Anxiety Sensitivity Treatment | Health Education TreatmentUnited States
-
Near East University, TurkeyCompletedType 1 Diabetes MellitusTurkey
-
University of DelawareCompletedDevelopmental Delay | Infant DevelopmentUnited States
-
Ankara UniversityCompletedEducation | Fertility | YouthTurkey
-
Marmara UniversityCompleted
-
Florida State UniversityOhio State University; Ohio UniversityRecruitingDementia | Anxiety | Alzheimer Disease | Mild Cognitive ImpairmentUnited States
-
Kessler FoundationThe Craig H. Neilsen Foundation; Kessler Institute for RehabilitationCompletedChronic Pain | Spinal Cord InjuryUnited States