U09.9
Conditions
Interventions
Group 1: - Patients with Long COVID
- PROMs and PREMs for evaluating the CLOCC healthcare model in the course of the project from year 2
Group 2: - Relatives
- Questionnaire evaluation of information
Sponsors
Universitätsmedizin Greifswald
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Presence of Long COVID - Ability to understand and follow the nature of the study and the procedures associated with the study - Suspected COVID-19 disease at least 3 months prior to study inclusion - Signed written informed consent form
Exclusion criteria
Exclusion criteria: - Insufficient German language skills to complete the questionnaires; assessed by the study staff - Current SARS-CoV-2 infection or positive test for SARS-CoV-2
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| -Patient Reported Outcome Measures (PROMs) -Patient Reported Experience Measures (PREMs) -Positive feedback from medical and therapeutic professionals (via the evaluation) -Sustainability concept for the continuation of CLOCC at the University Medical Centre and for nationwide implementation as part of standard care | — |
Secondary
| Measure | Time frame |
|---|---|
| - Reduction of the waiting time to obtain information from the CLOCC to 1 year after the date of introduction of the CLOCC - Organisation of information events and case conferences - Availability of information material on various topics and in different formats (paper-based, pdf, website) - Development of an innovation model for innovation adoption for CLOCC, on the basis of identified promoters and barriers - Analysis of direct and indirect costs of CLOCC - Cost-benefit assessment of the CLOCC | — |
Countries
Germany
Contacts
Public ContactPetra Lücker
Physikalische und Rehabilitative Medizin, Klinik und Poliklinik für Orthopädie, Unfallchirurgie und Rehabilitative Medizin, Universitätsmedizin Greifswald
Outcome results
None listed