Development of intersectoral medical care for patients with chronic critical illness
Not Applicable
Recruiting
- Conditions
- post intensive care syndromeJ44.9G62.80G72.80Z99.1Chronic obstructive pulmonary disease, unspecifiedDependence on respirator
- Registration Number
- DRKS00029326
- Lead Sponsor
- Charité - Universitätsmedizin Berlin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 57
Inclusion Criteria
Consenting and non-consenting patients who have a guardian or a proxy.
The patients are all of legal age and long-term ventilated.
All male and female, sick and long-term ventilated residents of the participating ventilator communities can be included.
Parallel participation in another study is possible. All health insurance providers are possible.
Exclusion Criteria
Refusal by the patient or their authorised representative or carer.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Access to measurement of PROMs: <br>Proportion of patients for whom PROMs were recorded 3 months prior to the defined measurement time points (or, if shorter, since admission to the facility), based on medical records. <br><br>Rehospitalisation:<br>Number of inpatient admissions within 3 months before the respective measurement date (or, if shorter, since admission to the facility), based on medical records.
- Secondary Outcome Measures
Name Time Method