K50 K51 K52
Conditions
Interventions
Group 1: Doctor's practices and hospitals function as multicentre study centres. As part of a preliminary study, one physician is interviewed per study centre. Patients with chronic inflammatory bowel
Sponsors
Arbeitsgemeinschaft IBD D-A-CH (vertreten durch FORGA solutions GmbH)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Minimum age > 18 years - Cognitive receptivity - CED / IBD disease - Patient of one of the participating doctor's practices/hospitals - Willingness to participate in the patient survey
Exclusion criteria
Exclusion criteria: Non-existence of one of the inclusion criteria (see above)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Based on surveys of physicians and patients (pseudonymised questionnaires in paper form), the effect of instruments of integrated care will be investigated: - How does the use of integrated care instruments affect the quality of life of patients? - How does the use of integrated care instruments affect patient adherence and satisfaction? A minimum period of three months per study centre is planned for the patient surveys, starting individually per study centre. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints: Impact of instruments of patient orientation: - What instruments are used in practice to involve patients in care? - How do the instruments affect patients' quality of life? - How do the instruments affect patient adherence and satisfaction? Tertiary endpoint: - Which context factors (patient-related, e.g. severity; physician-related, e.g. doctor's practice size; region-related, e.g. care density, regional differences) influence the effectiveness of the instruments? | — |
Countries
Austria, Germany, Switzerland
Contacts
Public ContactCarsten Schultz
Christian-Albrechts-Universität zu Kiel, Institut für Innovationsforschung, Professur für Technologiemanagement
Outcome results
None listed