NCT07098312

Brief Summary

The type of this research is a randomized controlled experimental study. The research aims to evaluate the effectiveness of creative drama workshops based on Papadopoulos' model on the cultural competence levels of nursing students. The population of the research consists of senior nursing students. The research sample will consist of at least 80 nursing students, 40 in the intervention group and 40 in the control group. The sample will be selected by randomization. 8 sessions of creative drama intervention will be applied to the students in the intervention group. The research aims to answer the following questions: Is there a difference between the intervention group and the control group in terms of cultural competence levels?

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 21, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

August 1, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

November 1, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2026

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

September 29, 2025

Status Verified

September 1, 2025

Enrollment Period

2 months

First QC Date

July 21, 2025

Last Update Submit

September 24, 2025

Conditions

Keywords

creative dramacultural competencynursing students

Outcome Measures

Primary Outcomes (1)

  • Cultural Competence Assessment Scale (CCAS)

    The CCAS assesses cultural competence in four dimensions-cultural awareness, knowledge, sensitivity, and practice-each with 10 items. A total score is obtained by summing the scores from all sub-dimensions. If the score from cultural awareness is below 5, the person is classified as having "Cultural Inadequacy," regardless of other scores. A total score of 40 across all dimensions indicates "Cultural Competence." If the cultural awareness score is 5 or more and all of the first four items in the knowledge, sensitivity, and practice sub-dimensions are answered correctly, the level is defined as "Cultural Security." If the awareness score is 5 or more but there are incorrect answers among the first four items in the other sub-dimensions, the level is considered "Cultural Awareness."

    six months

Study Arms (2)

Creative drama group

EXPERIMENTAL

Participants will be given eight sessions of creative drama intervention training in creative drama workshops reviewed by experts.

Behavioral: creative drama

Control group

NO INTERVENTION

No intervention will be applied to the control group.

Interventions

creative dramaBEHAVIORAL

It is aimed to develop cultural competence in nursing students through creative drama workshops.

Also known as: drama
Creative drama group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being a senior nursing student
  • Participating in the study voluntarily
  • Having a score below the average of the research population on the Cultural Competence Assessment Scale.

You may not qualify if:

  • Having a diagnosed physical, mental, or psychological disorder
  • Having previously received cultural competency training

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gazi University

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Psychodrama

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsPsychotherapy, GroupSocioenvironmental TherapyPsychotherapyBehavioral Disciplines and Activities

Central Study Contacts

Şeyma Nur Hepokur Yıldırım, PhD Candidate

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Due to the nature of the study, it is impossible to blind the researcher implementing the intervention and the participants. A pre-test will be administered before randomization to prevent bias in the study. The study's data collection and statistical process are planned to be blinded. The assignment of students to the intervention and control groups will be made by a statistician independent of the study. The researcher and the students will not know which group they are in until the application begins. After administering the follow-up tests, the independent researcher will code the data as groups A and B and transfer it to SPSS. With this method, the statistician plans to perform analysis and reporting without knowing which group is the intervention group and which is the control group. The codes of the groups are intended to be disclosed after the analysis and reporting of the data. In this way, detection bias, statistical bias, and reporting bias will be prevented.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Randomized study with experimental and control groups
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof.

Study Record Dates

First Submitted

July 21, 2025

First Posted

August 1, 2025

Study Start

November 1, 2025

Primary Completion

January 1, 2026

Study Completion

April 1, 2026

Last Updated

September 29, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

IPD sharing is restricted by data confidentiality, participant privacy, and applicable ethics rules and legislation. Sharing data with third parties may require relevant ethics committee approval, institutional permissions, and explicit consent from participants. If these conditions are not met, IPD sharing may not be possible.

Locations