Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:18 PM
Ignite Modification Date:
2026-03-26 @ 3:18 PM
NCT ID:
NCT07435558
Eligibility Criteria:
Inclusion Criteria:
1. written informed consent;
2. at least one year of clinical nursing experience;
3. availability to attend all scheduled workshop sessions (no planned extended leave during the intervention period);
4. completion of the Index of Learning Styles (ILS) questionnaire and availability of valid ILS scores for group allocation
Exclusion Criteria:
1. attendance in a similar PBL or patient-safety educational program within the previous 6-12 months;
2. significant uncorrectable hearing or vision impairment or severe cognitive/psychiatric condition that precluded participation;
3. concurrent participation in another interventional study likely to affect study outcomes;
4. repeated non-attendance (\>2 missed sessions) or voluntary withdrawal after randomization.
Healthy Volunteers:
True
Sex:
ALL
Study:
NCT07435558
Study Brief:
Protocol Section:
NCT07435558