Clinical Trials Directory

Trials / Completed

CompletedNCT02134587

Educational Intervention in Pharmacovigilance for Hospital Health Professionals

Implementation of a Hospital Pharmacovigilance Service and Comparison of Algorithms for Adverse Drug Reaction Causality Assessment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
203 (actual)
Sponsor
Universidade Estadual Paulista Júlio de Mesquita Filho · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Spontaneous reports by health professionals generate the signals in pharmacovigilance. However, the passive method has limitations and the most important of them are the underreporting and the poor quality of data, hindering the causality assessment of adverse drug events (ADE). Therefore, the present study aimed to validate an educational intervention (EI) in pharmacovigilance for hospital health professionals, in order to analyze the impact on the knowledge, skill and attitude in ADE reporting. Investigators proposed a multifaceted EI which will be developed in four meetings with one hour each. The following activities will be carried out: application of a questionnaire to assess the knowledge, skill and attitude before and after EI; lecture; practical class and education material distribution. The answers of questionnaire are going to be analyzed using content analysis technique. The definitions of World Health Organization and the minimum and desired criteria to fill the ADE form, according to the Pan American Health Organization, are going to be considered gold-standard answers. The statistical test of Wilcoxon-Mann Whitney test for paired samples will be applied, in order to assess the impact of educational intervention on behavior of health professionals (ADE reporting). With the present study, the following hypotheses will be tested: H0= There is no difference between the numbers of ADE reported (behavior/attitudes) before and after the educational intervention. H1= The numbers of ADE reported before and after the educational intervention are different.

Detailed description

A quasi-experimental study with health professionals who acted in a general and public hospital of medium complexity with 104 beds will be performed. Investigators proposed an educational intervention, with the development of lecture and practical class, application of questionnaire before and after EI and the distribution of educational material. Activities will be developed in four meetings of one hour each one. In the first meeting, questionnaire will be applied, in order to assess knowledge, skills and attitudes in pharmacovigilance prior to EI. The instrument was elaborated based on previous studies. Second meeting will be comprise a lecture regarding the theoretical framework and importance of pharmacovigilance, and distribution of educational material, whose content includes the same issues of presentation. In the third meeting, a practical class will be performed to promote a discussion of a fictitious case of adverse drug reaction (ADR), in order to elucidate the correct fill of ADE form. In the fourth meeting, will be repeated the application of questionnaire, in order to assess the impact of EI. With the aim to verify change behavior of health professionals regarding pharmacovigilance activities, the number of ADE reports made prior and after intervention will be compared.

Conditions

Interventions

TypeNameDescription
OTHERMultifaceted educational intervention1. Application of questionnaire of knowledge, attitudes and skills in pharmacovigilance. 2. Lecture regarding the theoretical framework and importance of pharmacovigilance, and distribution of educational material 3. Distribution of educational material 4. Practical class to explain the correct fill of adverse drug events form 5. Reapplication of questionnaire of knowledge, attitudes and skills in pharmacovigilance.

Timeline

Start date
2012-02-01
Primary completion
2013-09-01
Completion
2014-05-01
First posted
2014-05-09
Last updated
2023-06-05
Results posted
2015-08-20

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02134587. Inclusion in this directory is not an endorsement.