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Clinical Trials/NCT02339792
NCT02339792
Completed
N/A

Effect of an Integrated E-learning Intervention, Focused on Comprehensive Geriatric Assessment to Improve the Quality of Drug Prescribing in Hospitalized Elderly Patients

Mario Negri Institute for Pharmacological Research0 sites697 target enrollmentNovember 2012
ConditionsDrug Use

Overview

Phase
N/A
Intervention
Not specified
Conditions
Drug Use
Sponsor
Mario Negri Institute for Pharmacological Research
Enrollment
697
Primary Endpoint
Improvement of drug prescribing
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This randomized controlled pragmatic study is aimed to set-up, assess and implement an integrated e-learning program of medical education in an hospital setting, focused on teaching and implementing CGA added to geriatric pharmacological notions (GPNs) to improve the quality of drug prescribing in elderly patients

Detailed Description

The integrated e-learning program (intervention group) is focused on teaching and implementing knowledge on CGA and GPNs to help clinicians to improve the quality of drug prescribing in the elderly.The GPNs is focused on pharmaco-epidemiological issues of drug prescribing, pharmacokinetic and pharmacodynamic changes during aging, topics in evaluating and managing polypharmacy, criteria to review the appropriateness of drug therapies and the clinical relevance of PDDI in the elderly. The control group receives only GPNs.

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
September 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Mario Negri Institute for Pharmacological Research
Responsible Party
Principal Investigator
Principal Investigator

Paola Boccardo

MD

Mario Negri Institute for Pharmacological Research

Eligibility Criteria

Inclusion Criteria

  • people aged 75 years or older

Exclusion Criteria

  • people aged 75 years or older
  • refusal of consent to participate
  • a life expectancy of less than 6 months

Outcomes

Primary Outcomes

Improvement of drug prescribing

Time Frame: Participants will be followed for the duration of hospital stay, an expected average of 12 days

The primary study objective is to evaluate whether an integrated e-learning program of medical education, focused on teaching and implementing CGA added to GPNs (intervention) is superior to delivering GPNs only (control) in reducing the prescription of potentially inappropriate medications (PID) or of potential drug-drug interactions (PDDI) during hospitalization and at hospital discharge in hospitalized elderly. The primary outcome is the change in prescription of PID,as defined by Beers' criteria , or of PDDI related to the 20 drugs most frequently prescribed during hospital stay and at discharge.

Secondary Outcomes

  • clinical outcomes (lenght of hospitalization, mortality, rehospitalization)(12 months)

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