Health-care Quality in Semi-intensive Care Units
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Semi-intensive Care Unit, Evaluation, Quality. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Evaluation and Improvement of the Health-care Quality in Semi-intensive Care Units
Overview
The main aim of this study is to realize a system of continuous evaluation of healthcare quality in semi-intensive care units.
Detailed description
Collecting data of semi-intensive care units' patients and structural data of hospitals, healthcare quality's indicators will be realized. Starting from those indicators of insuccess, specific for different kinds of patients, it will be possibile to evaluate the general level of care in each singular semi-intensive care unit. The study will least for 5 years, but at the end of every year it will be realized a report of analysis to see the results of each unit.
Primary outcome measures
- Outcome for stationary patients with high risk of variability [Time frame: jan 2021 - dec 2025]
- Outcome for low gravity patients, with a low organ's damage [Time frame: jan 2021 - dec 2025]
- Outcome for semi-intensive patients [Time frame: jan 2021 - dec 2025]
- Outcome for high risk patients [Time frame: jan 2021 - dec 2025]
Eligibility criteria
Inclusion criteria
- all patients hospitalised in a semi-intensive care unit
Exclusion criteria
- None
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Italy · 18 centers
- Istituto di Ricerche Farmacologiche Mario Negri IRCCS — Milan
- ASO SS Antonio e Biagio e Cesare Arrigo — Alessandria
- Ospedale San Bassiano — Bassano del Grappa
- Ospedale Maggiore — Bologna
- AOU Policlinico S. Marco — Catania
- Ospedale Bufalini — Cesena
- Ospedali Riuniti — Livorno
- ASST Lodi — Lodi
- … and 10 more centers
Identifiers
NCT: NCT04676347 · IRFMN_7998