NCT07461974

Brief Summary

Cancer pain is a significant clinical problem that directly affects patients' quality of life and requires nurses to be equipped with adequate knowledge and skills to provide effective care. The current shift in knowledge and skill acquisition from traditional teaching methods toward e-learning-based approaches has increased the importance of comparing the effects of these educational methods on learning outcomes in cancer pain management education. Within this context, the course content on cancer pain management will be developed using both traditional and e-learning methods based on the ADDIE instructional design model. The effects of these two methods on students' learning outcomes and institutional teaching costs will be evaluated. Thus, this study aims to contribute to identifying effective and cost-efficient teaching strategies in nursing education.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
7mo left

Started Jun 2026

Shorter than P25 for not_applicable

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

March 4, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 10, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

June 1, 2026

Expected
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

March 10, 2026

Status Verified

March 1, 2026

Enrollment Period

7 months

First QC Date

March 4, 2026

Last Update Submit

March 9, 2026

Conditions

Keywords

NursingTraditional Learning MethodsE-Learning MethodsEducationCost

Outcome Measures

Primary Outcomes (5)

  • Cancer Pain Knowledge Test

    The test, which will be developed by the researchers based on the literature, was prepared in two stages. In the first stage, multiple-choice questions were developed by the researchers based on the expected learning outcomes related to the cancer pain topic taught in the Internal Medicine Nursing course and the resources used in the course. In the second stage, an expert panel consisting of five faculty members from the field of Internal Medicine Nursing was formed to evaluate the content validity of the test. The experts assessed the content validity of the test using the Davis technique, and their suggestions for revision or modification were obtained. The expert evaluations were analyzed using the Content Validity Index, and the final version of the knowledge test was established based on the experts' feedback. The test consists of 20 questions, with scores ranging from a minimum of 0 to a maximum of 100. Higher scores indicate greater knowledge.

    Twice, once at the end of the training (day 1) and again after 4 weeks.

  • Scenario-Based Assessment of Practical Skills Form

    The learning outcomes related to cancer pain education identified by the researchers were used as the basis for developing a scenario lasting approximately 25-30 minutes and a corresponding skill evaluation checklist. The prepared scenario and checklist will be evaluated in terms of scope and content by a group of experts in the field. During the implementation phase, students will provide care to a patient with cancer pain described in the scenario. The students' practical skills during the scenario will be assessed using the skill evaluation checklist by one evaluator and one observer, who are nursing educators and are independent of the researchers. The maximum score that can be obtained from the application is 100, and the minimum score is 0. Higher scores indicate higher skill levels.

    Twice, once at the end of the training (day 1) and again after 4 weeks.

  • Motivation Scale Regarding Instructional Material

    The scale was developed by Keller in 2006 to measure motivation toward instructional materials. In 2016, it was adapted into Turkish by Dinçer and Doğanay. The original version of the scale consists of 36 items in a five-point Likert format; however, during the Turkish adaptation process, three items were removed. The scale consists of four subdimensions: attention, relevance, confidence, and satisfaction. Items 3, 7, 12, 15, 19, 22, 26, 29, 31, and 34 are negatively worded and require reverse scoring. The minimum possible score on the scale is 36 and the maximum score is 180, with a midpoint of 108.00. The internal reliability coefficient of the scale was calculated as 0.93.

    once at the end of the training (day 1)

  • Institutional Cost Information Form

    To determine the cost of education, a Cost Information Form was developed based on the literature and expert opinions, taking into account the institutional costs incurred for students' education. The expenditure items included in the form will be calculated in Turkish Lira.

    at the end of the study

  • Visual Analog Scale

    Students will evaluate the instructor's performance by marking a point between 0 and 10 on a continuous line between two endpoints. Higher scores indicate better educator performance, while lower scores indicate poorer educator performance.

    once at the end of the training (day 1)

Study Arms (2)

e-learning group

EXPERIMENTAL

For the e-learning method, the cancer pain management course will be delivered through a web-based platform designed according to the ADDIE model, using artificial intelligence-supported avatar lectures and gamified case scenarios.

Behavioral: e-learning

traditional group

ACTIVE COMPARATOR

For the traditional method, the cancer pain management course will be delivered through classroom lectures and case scenarios designed according to the ADDIE model.

Behavioral: traditional group

Interventions

e-learningBEHAVIORAL

For the e-learning method, the cancer pain management course will be delivered through a web-based platform designed according to the ADDIE model, using artificial intelligence-supported avatar lectures and gamified case scenarios.

Also known as: Educational intervention in cancer pain management training
e-learning group

For the traditional teaching method, the cancer pain management course will be delivered through classroom lectures and case scenarios designed according to the ADDIE model.

Also known as: Educational intervention in cancer pain management training
traditional group

Eligibility Criteria

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

You may qualify if:

  • Students who have access to the internet and a computer/mobile phone,
  • Students who have successfully completed the Fundamentals of Nursing course,
  • Students who are taking the Internal Medicine Nursing course for the first time,
  • Students who voluntarily agree to participate in the study.

You may not qualify if:

  • Students who are repeating the Internal Medicine Nursing course,
  • Students who have taken the Palliative Care and Nursing or Oncology Nursing courses,
  • Students who have been diagnosed with cancer themselves or have a relative diagnosed with cancer,
  • Students who were admitted to the nursing department through the Vertical Transfer Exam (DGS) after graduating from an associate degree program in a health-related field,
  • Students who graduated from a Vocational Health High School,
  • Students who were admitted through the International Student Examination.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Cancer Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Semanur Bilgiç, Research Asisstant

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

March 4, 2026

First Posted

March 10, 2026

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

March 10, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share