Medication Safety
Conditions
Interventions
Group 1: Patients who participate in the ATHINA project, study-specific surveys, and follow-up assessment.
Group 2: Comparable patients who do not participate in the ATHINA project but fill in the ano
Sponsors
Abteilung Klinische Pharmakologie und Pharmakoepidemiologie, Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Agreement to participate; Generally, elderly patients with higher risk for medication related Problems are invited to participate in the ATHINA Projects and likewise, these patients are also invited to participate in the accompanying study
Exclusion criteria
Exclusion criteria: < 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of recommended measures realization and patient satisfaction (sims-d questionnaire) change between study start and after 3-6 month (follow-up assessment). | — |
Secondary
| Measure | Time frame |
|---|---|
| Process and medication related parameter: number and type of medication related Problems; time exposure and pharmacist satisfaction; analysis of predictors for a successful ATHINA project realization; patient related parameter: change of medication related quality of life and patient satisfaction during the project and compared to patients who do not participate in the ATHINA project | — |
Countries
Germany
Contacts
Public ContactHanna Seidling
Universitätsklinikum Heidelberg, Abteilung Klinische Pharmakologie und Pharmakoepidemiologie, Kooperationseinheit Klinisch Pharmazie
Outcome results
None listed