About this trial
This study evaluates the impact of a structured interprofessional training program on daily collaboration within the Cardiac Intensive Care Unit (CICU/UTIC) at the University Hospital of Parma. In high-intensity clinical settings, rapid and accurate coordination between physicians, nurses, and healthcare assistants is vital. Ineffective teamwork often leads to communication breakdowns, potentially compromising patient safety and care quality. This project investigates whether an interactive, scenario-based educational program can strengthen role clarity, communication, and shared decision-making.
The study seeks to determine if an active-learning program using interactive branching scenarios improves interprofessional collaboration more effectively than traditional methods. The researchers hypothesize that this simulation-based approach will significantly enhance professional outcomes, including self-efficacy, shared decision-making, and commitment to both the team and the profession.
The study utilizes a convenience sample (approx. 5 physicians, 30 nurses, 8 healthcare assistants, and 10 students). Eligible participants include staff and students currently or recently active in the Parma CICU who provide informed consent.
The intervention is delivered via a Moodle-based platform featuring case-based simulations. These scenarios replicate complex clinical pathways, such as:
Cath-lab and Electrophysiology procedures.
Heart failure management.
TAVI (Transcatheter Aortic Valve Implantation) preparation.
As participants navigate these scenarios, they must make critical decisions and receive immediate feedback designed to reinforce collaborative best practices.
Data Collection and Timeline
Data is gathered at three intervals: T0 (Baseline), T1 (Post-training), and T2 (6-month follow-up). Validated questionnaires measure:
Attitudes toward physician-nurse collaboration.
Perceived daily collaboration and decision-making satisfaction.
Professional commitment and work-related self-efficacy.
The training phase spans six months, with a subsequent six-month follow-up, totaling a 24-month project duration.
Ethics and Privacy Risks are minimal, primarily involving the time required for participation. The primary benefit is the development of skills that foster safer, more coordinated patient care. Privacy is strictly maintained through pseudo-anonymization, with data access restricted to the research team.
Eligibility criteria
Qualifiers
Healthcare professionals (physicians, nurses and healthcare assistants/OSS) employed in the Cardiac Intensive Care Unit (UTIC) of the University Hospital of Parma.
Healthcare professionals who have completed the training pathway and are still working in the unit at the time of the six-month follow-up.
Medical and nursing students who have carried out or are carrying out a clinical placement within the UTIC.
Ability to use a computer or mobile device, essential for participating in the online training activities (e.g. Moodle, H5P).
Disqualifiers
Healthcare professionals who do not work in the cardiology setting or who are not employed in the UTIC of the AOU Parma.
Inability to participate in the training activities or assessment sessions for logistical, organisational or clinical reasons (e.g. planned prolonged absences during the study period).
Refusal or inability to provide informed consent.
Trial design
Treatments tested in this trial
- The training phase of the project consists of an interactive course aimed at healthcare professionals (physicians, nurses and OSS) to improve their ability to recognise and enact effective collaborati