No registrations found.
ID
Source
Brief title
Health condition
cancer, lung diseases
Sponsors and support
Agis-zorgverzekeringen
Intervention
Outcome measures
Primary outcome
1. Difference in knowledge about prescribed medicines between intervention and control group at measurement II, per patient corrected for the basis at measurement I
(method: questionnaires);
2. Differences in correct use of medicines between intervention and control group at measurement III
(method: questionnaires).
Secondary outcome
1. Differences in spotting and reporting medication deviations during the distribution of medicines in hospital between intervention and control group (measurement II);
2. Differences in satisfaction about the received information about medicines (measurement II).
Background summary
Additional information design:
3 measurements at the departments of lung diseases and oncology during intervention period as well as control period.
Measurement I: 1-3 days after admission.
Meaurement II: during discharge.
Measurement III: during re-admission or control visit.
Size of the 4 groups: 60 patients per department and apart for intervention en control (power calculation).
Study objective
The intervention lead to:
1. More knowledge about (the use of) prescribed medicines;
2. A better use of medicines during the stay in the hospital and after discharge.
Study design
N/A
Intervention
1. Personalized computer generateed medications reminder charts during admission and discharge and brochures about specific medicines;
2. Patient safety chart with instructions for safe and correct use of medicines.
The intervention measurements at the departments of lung diseases and oncology lasts three months. The control measeruments lasts three months (same departments).
Universiteit Utrecht
Heidelberglaan 1
Utrecht 3584 CS
The Netherlands
Universiteit Utrecht
Heidelberglaan 1
Utrecht 3584 CS
The Netherlands
Inclusion criteria
1. Admission at one of the participating departments;
2. Informed consent;
3. Duration of admission at least 3 days maximally a month.
Exclusion criteria
1. Patients younger than 18 years;
2. Patients who are emotionally or physically not capable to participate;
3. Senile dementia, confusion of the patient;
4. Inability to express in Dutch language.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL766 |
NTR-old | NTR777 |
Other | : N/A |
ISRCTN | aanpassingen ISRCTN04371570 |