Polypharmacy Other
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with intake of =8 systemically available drugs (in case of combination products, =8 active ingredients, also including over-the-counter drugs, especially if they are on the list of interaction relevant over the counter drugs) 2. Patients >18 years of age 3. Patients signing informed consent
Exclusion criteria
Exclusion criteria: 1. Patients not willing to adhere to the study’s requirements 2. Patients unable to understand the nature and purpose of the study 3. Previous participation in a structured medication review type 2a
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Drug-related problems assessed using a structured medication review type 2a (questionnaire) at baseline, after 3 to 4 months, and after 6 to 9 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Therapy adherence assessed using a structured medication review type 2a (questionnaire) at baseline, after 3 to 4 months, and after 6 to 9 months 2. Health literacy was assessed using a structured medication review type 2a (questionnaire) at baseline, after 3 to 4 months, and after 6 to 9 months 3. The effects of one structured medication review type 2a at months 3 to 4 compared to two structured medication reviews type 2a at baseline and month 3 to 4 on drug-related problems (questionnaire) 4. The number of drug-related problems assessed using a structured medication review type 2a (questionnaire) at baseline, after 3 to 4 months, and after 6 to 9 months 5. The number of medications and active ingredients assessed using a structured medication review type 2a (questionnaire) at baseline, after 3 to 4 months, and after 6 to 9 months 6. Relative and absolute frequency of contraindications or severe drug-related problems that require intervention by clinical pharmacologists/clinical pharmacists or treating physicians, assessed using a structured medication review type 2a (questionnaire) at baseline, after 3 to 4 months, and after 6 to 9 months 7. Associations of gender, age, and number of medications/active ingredients at baseline with the number of drug-related problems assessed using a structured medication review type 2a at baseline Added 26/03/2025: 1. Descriptive statistics of patients participating in part 2 of the study per group and presentations of reasons why the study was terminated before part 1 2. Absolute and relative number of contributors to drug-related problems (e.g., double prescriptions, dosing errors, etc) and the impact of a structured medication review type 2a (questionnaire) on these parameters at baseline, after 3 to 4 months, and after 6 to 9 months 3. Change in drug-related problems (or contributors) within each group from baseline to month 3 to 4 or month 6 to 9 using a structured medication review type 2a (questionnaire) will be analyse | — |
Countries
Austria