Comparative Case Learning in Undergraduate Nursing Students

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAgri Ibrahim Cecen University

About this trial

This randomized controlled educational trial compares two ways of teaching undergraduate nursing students to reason through clinical cases. Both study arms receive the same eight training cases, the same total instructional time, and the same individualized feedback on their answers. Students in the comparative-case arm study the training cases in matched pairs and explicitly write both the finding that changes the recommended first action and the general principle it illustrates. Students in the individual-case arm reason through and justify each training case on its own, with the same content and time. Four baseline cases are completed before training, and eight new transfer cases are completed seven days after training (acceptance window Day 5-9). The single primary outcome is a 0-100 reasoned clinical decision transfer score at Day 7, derived from two independent, blinded raters. The trial targets 360 randomized nursing students (Years 1-4) at a single site, and the primary analysis will estimate the between-group difference in transfer score adjusted for baseline performance, class year, and session block. The study evaluates whether making the decision-relevant contrast between paired cases explicit improves near transfer of clinical reasoning under matched content and time; it does not involve real patients or clinical interventions, and it does not produce direct conclusions about real-world patient safety or general clinical competence.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Currently enrolled undergraduate nursing student (1st through 4th year)

Age 18 years or older

Sufficient Turkish reading and comprehension ability to complete study materials

Willing and able to provide written informed consent

Disqualifiers

Does not provide informed consent

Prior participation in the pilot study for this research

Prior exposure to the clinical case scenarios used in this study

Trial design

Design model

Parallel

Treatments tested in this trial

  • Comparative Case Learning Educational Package

    Behavioral

    Printed, coded booklets presenting the same eight training cases as four paired comparisons. For each pair, students write their priority approach to each case plus the case-deciding difference and its general principle (four response fields per pair, \~20 words each, 6 minutes per pair). Same clinical content, response burden, and individual case feedback as the active comparator.

  • Individual Case Reasoning Educational Package

    Behavioral

    Printed, coded booklets presenting the same eight training cases one at a time on separate pages. For each case, students write their priority approach and a short rationale in two response fields (\~20 words each, 3 minutes per case). Same clinical content, response burden, and individual case feedback as the experimental arm, without paired comparison prompts.

Treatment groups

360 Participants
are divided into 2 treatment groups
Group A: Comparative Case Learning (Arm K)Experimental treatment 1 intervention
Group B: Individual Case Reasoning (Arm B)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Reasoned Clinical Decision Transfer Score

Composite 0-100 score on eight new (untrained) clinical cases at Day 7, integrating each case's priority-approach and reasoning on a 0-3 rubric (0-24 raw total), averaged across two independent, arm-blinded raters and rescaled to 0-100. Higher scores indicate better transfer of reasoned clinical decision-making to novel cases.

Time frame
Day 7 post-training (acceptance window: Day 5-9)

Secondary outcomes

1

Rate of Appropriate Initial Approach on New Cases

Proportion of the eight Day-7 cases in which the student's initial approach is judged correct by both raters (1 if correct, 0 if not, averaged across two raters), reflecting decision accuracy separate from the composite reasoning score.

Time frame
Day 7 post-training (acceptance window: Day 5-9)
2

Rate of Delayed Help-Seeking in Emergent Cases

Among the four emergent Day-7 cases, the proportion of responses that delay calling for help or urgent assessment in favor of routine measures or repeating an assessment, scored 1 if delayed / 0 if not, averaged across two raters.

Time frame
Day 7 post-training (acceptance window: Day 5-9)
3

Rate of Unnecessary Emergency Escalation in Non-Emergent Cases

Among the four non-emergent Day-7 cases, the proportion of responses that escalate to an emergency call or urgent treatment without a stated rationale, scored 1 if unwarranted escalation / 0 if not, averaged across two raters.

Time frame
Day 7 post-training (acceptance window: Day 5-9)

Other outcomes

Sponsors and contacts

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