R13.9
Conditions
Interventions
Group 1: Observational group:
All patients answer a questionnaire and a short additional questionnaire.
All physicians answer a short questionnaire concering the different patients (same questions).
Sponsors
Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Full age, Chronic intake of at least one drug for the duration of at least four weeks
Exclusion criteria
Exclusion criteria: Non adults, No drug intake for the duration of at least four weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Prevalence of problems swallowing solid oral dosage forms 2. Relevance of swallowing difficulties Data of both primary endpoints will be collected during the duration of the study with a questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Dependence of pharmaceutical formulations on swallowing difficulties 2. Dependence of active ingredients on swallowing difficulties 3. Dependence of swallowing mistakes on swallowing difficulties 4. Dependence of diseases on swallowing difficulties 5. Correlation between mental factors and swallowing difficulties 6. Patients‘ consciousness of effects of modifications 7. Physicians‘ and pharmacists‘ consciousness of swallowing difficulties 8. Preference for certain pharmaceutical dosage forms All endpoints will be collected during the duration of the study with a questionnaire. | — |
Countries
Germany
Contacts
Public ContactJulia Schiele
Universitätsklinikum Heidelberg
Outcome results
None listed