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Polypharmacy reduction in patients treated for chronic diseases

Polypharmacy reduction in patients treated for chronic diseases ? a patient-centered approach utilizing the interface between secondary and primary care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN42003273
Enrollment
1626
Registered
2014-01-30
Start date
2014-08-01
Completion date
Unknown
Last updated
2017-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with chronic diseases and polypharmacy (= 5 prescribed long-term drugs) Not Applicable

Interventions

During in-patient treatment of chronically ill patients affected by polypharmacy, a pharmacist specially trained in communication skills performs a narrative-based medication review. Apart from detect

Sponsors

German Federal Ministry of Education and Research (BMBF) (Germany)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Two local hospitals will recruit patients with chronic diseases and polypharmacy meeting the following inclusion criteria: 1. Aged 60+ years 2. Taking = 5 prescribed long-term drugs 3. Likely to spend at least one week in the hospital

Exclusion criteria

Exclusion criteria: 1. Inability to take their medication by themselves 2. Inability to give informed consent (e.g. due to dementia) 3. Severe language difficulties 4. Diseases that usually make poly-pharmacotherapy unavoidable (e.g. active malignoma, acquired immunodeficiencies [HIV], hemodialysis) 5. Presumed life expectancy of less than 12 months Added 20/01/2017: 6. Patients being diagnosed with any type of cancer after recruitment will be excluded from the study

Design outcomes

Primary

MeasureTime frame
The two independent main outcomes are: 1. Health-related quality of life, measured using the EQ-5D 2. The difference in the number of prescribed long-term pharmaceutical agents between intervention and control group at T3. Primary outcome is defined as pharmaceutical agents rather than number of drugs because combination drugs are commonly used in Germany. During the baseline and intervention periods, primary outcomes for each patient will be measured at four points in time: at admission to the hospital (T0) and discharge from hospital (T1), as well as 6 (T2) and 12 months (T3) after discharge from the hospital.

Secondary

MeasureTime frame
1. Appropriateness of prescribed medication 2. Patient satisfaction 3. Patient empowerment 4. Patient autonomy 5. For all patients insured with the largest public German health insurance provider AOK, cost effectiveness and further aspects of quality of care will be analyzed Measured at T0, T2 and T3

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 7, 2026