Clinical trials

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Status: Not yet recruiting

Patient Satisfaction Study at AOU Maggiore Della Carità (SCORE)

The general aim of this study is to assess and analyze the level of patient satisfaction with nursing care among inpatients in the ordinary wards of the AOU Maggiore della Carità in Novara (Italy). Using the validated Newcastle Satisfaction with Nursing Scales (NSNS), the study intends to produce reliable and comparable data that reflect patients' perceived quality of care across multiple dimensions, including relationships, emotional support, information, and time devoted by nurses. The study aims to provide an updated overview of patient experiences, identifying strengths and areas for improvement. These results will offer guidance for organizational and educational strategies to promote more personalized, human-centered nursing care aligned with international quality and safety recommendations, without altering routine clinical practice.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Università degli Studi del Piemonte Orientale Amedeo AvogadroUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Adult inpatients (age ≥ 18 years) admitted to ordinary wards of AOU Maggiore del... [+3]

Hospitalization shorter than 48 hours. [+3]

Status: Recruiting

Hypnotic Communication in Cardiology: A Randomized Controlled Trial

Undergoing medical procedures, especially surgical ones, is a significant source of emotional stress for patients. Emotions like anxiety, fear, anger, and depression often accompany such experiences and can negatively impact clinical outcomes. Preoperative anxiety, in particular, affects nearly half of all surgical patients and can lead to complications such as hemodynamic instability, increased medication needs, and prolonged recovery times. Managing this emotional distress is therefore a priority. While pharmacological strategies are commonly used, growing attention is being given to non-drug interventions such as music, art, and play therapies. One such technique is hypnotic communication-a method that uses empathetic, suggestion-based language to influence emotional and physical states without formal hypnotic induction. This technique has roots in anesthesiology and has shown promise in reducing pain and anxiety during medical procedures. The proposed study aims to evaluate the effectiveness of hypnotic communication in reducing emotional distress in patients undergoing elective coronary angiography. This will be done through a randomized controlled trial involving 306 adult patients at the Cardiology Unit of the Ospedale degli Infermi in Biella, Italy. Participants will be randomly assigned to either an experimental group receiving hypnotic communication alongside standard care, or a control group receiving standard care only. The hypnotic session, delivered by trained nurses, will begin before the procedure and continue until it ends, following a five-phase structure (pre-induction, induction, core, de-induction, and closure). The primary outcome is the patient's emotional state-specifically stress, anxiety, depression, anger, and need for help-measured before and after the procedure using the Emotion Thermometer Tool. Secondary outcomes include post-procedural pain (measured 15 and 60 minutes after) and patient satisfaction with the communication technique. The study is designed with a type I error rate of 0.05 and 80% statistical power, and recruitment is expected to last 24 months. Data will be anonymized, securely stored, and analyzed using appropriate statistical methods. Ethical approval and informed consent are integral parts of the protocol. By investigating the emotional and clinical impact of hypnotic communication, the study hopes to support its integration into routine care practices, offering a simple, safe, and cost-effective method to enhance patient well-being during invasive procedures.

Participants needed: 306
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Università degli Studi del Piemonte Orientale Amedeo AvogadroUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Adult patients (≥18 years), of both sexes, referred to the Cardiology Unit and s... [+1]

Cognitive impairment or neurodegenerative disorders that may compromise the abil... [+1]

Status: Recruiting

Acute DYSPnea in the Emergency Department: Diagnostic Value of Point-of-care UltraSound

Acute dyspnea is a common reason for emergency department (ED) admission and is frequently caused by acute heart failure with pulmonary edema. Rapid differentiation between cardiogenic and non-cardiogenic causes of dyspnea is essential to guide early treatment and risk stratification. However, no single gold standard exists for the assessment of venous congestion in the acute setting. This prospective observational study aims to evaluate the diagnostic accuracy of respiratory variation in inferior vena cava (IVC) diameter measured by point-of-care ultrasound (POCUS) in identifying acute pulmonary edema in patients presenting to the ED with acute respiratory failure. In addition, the study investigates whether integration of IVC ultrasound with lung ultrasound, bedside cardiac ultrasound, and selected clinical and laboratory variables - such as hemoglobin and plasma protein changes - improves diagnostic performance and prognostic stratification.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Università degli Studi del Piemonte Orientale Amedeo AvogadroUpdated: Jan 8, 2026Locations: 1
Eligibility criteria

Adults aged ≥18 years. [+5]

Refusal to provide informed consent (or consent by legal representative when app... [+4]

Status: Not yet recruiting

Nutritional Intake in Patients on Noninvasive Ventilation: a Prospective Observational Study

The primary objective is to quantify the caloric and protein intake in adult participants with acute respiratory failure who start a noninvasive ventilation treatment. The main question is: \- Are participants meeting their caloric and protein target during noninvasive ventilation treatment? Participants will complete a five-day food diary collection starting from the initiation of noninvasive ventilation treatment.

Participants needed: 126
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Università degli Studi del Piemonte Orientale Amedeo AvogadroUpdated: Dec 27, 2024Locations: 1
Eligibility criteria

Age of 18 years or more [+2]

Palliative noninvasive ventilation treatment [+3]