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The Cultural Sensitivity Education Program

S

Sultan Ayaz Alkaya

Status

Completed

Conditions

Intercultural Sensitivity

Treatments

Other: Intercultural Sensitivity Education Program

Study type

Interventional

Funder types

Other

Identifiers

NCT05993403
2023-558520

Details and patient eligibility

About

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.

Full 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.

Enrollment

64 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

Intercultural Sensitivity Education
Experimental group
Description:
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.
Treatment:
Other: Intercultural Sensitivity Education Program
Control
No Intervention group
Description:
Data collection tools were applied to this group before the research. No intervention was applied to this group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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