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:
2025-12-25 @ 4:08 AM
Ignite Modification Date:
2025-12-25 @ 4:08 AM
NCT ID:
NCT06878820
Eligibility Criteria:
Nurses and student nurses (vocational nursing educational level (MBO)/ (bachelor nursing educational level (HBO)):
Inclusion Criteria:
\- All (student-)nurses working in the participating wards are expected to be involved in application of FFC and role development with regards to leadership and autonomy of nurses and therefore considered to be eligible for participation in the study.
Exclusion Criteria:
\- No exclusion criteria were defined for nurses and student nurses.
Physiotherapists, doctors and other member of the interprofessional team;
Inclusion Criteria:
\- All professional groups that are part of the interprofessional team of the ward and who work in the participating wards are expected to collaborate with the nursing in their daily care and therefore considered to be eligible for participation in this study.
Exclusion Criteria:
\- No exclusion criteria were defined for physiotherapists, doctors and other members of the interprofessional team.
Patients and informal caregivers:
Inclusion Criteria:
\- All patients admitted to the participating wards of the 2 hospitals receiving care either before or after the implementation of FFC and the patients informal caregiver as determined by the patient.
Exclusion Criteria:
* A life-threatening situation or in a terminal phase upon admission (only applicable to patients)
* Not mastering the Dutch language;
* Not able to communicate adequately, based on a below threshold score on the MOCA or the FAST (only applicable to patients)
* A second hospitalization on one of the participating wards after being included in the study during the study period;
* An hospitalization \< 48 hours
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06878820
Study Brief:
Protocol Section:
NCT06878820