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Clinical Trials/NCT02484144
NCT02484144
Completed
Not Applicable

Evaluation of the Information of the Patient Before a Scheduled Coronarography

French Cardiology Society40 sites in 1 country821 target enrollmentJuly 2015
ConditionsCardiac Disease

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Disease
Sponsor
French Cardiology Society
Enrollment
821
Locations
40
Primary Endpoint
Improvement of the quality of the information of the patients
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

French study, multicentrique with the cooperation of several hospital centers . 700 patients (200 in the stage 1 and 500 in the stage 2). Every patient will complete questionnaires in a anonymous way.

Detailed Description

Stage 1: evaluation of the score in the population and the evaluation of the improvement of the score after an information more detailed by the educational video. For that purpose, inclusion on one week with comparison of the score obtained during a classic information with delivery of the sheet of information and during a classic information followed by an information more detailed with educational video. Check during this stage of the significant improvement of the score with the addition of the educational video literally of information and in the oral information supplied usually within the framework of the current care Evaluation of the number of subject included in the 1 week. Stage 2: Comparison of the patient understanding between 2 groups: 1 group received the information by using the information targeted with educational video (modern information) and the other group the classic information considered as the reference. Inclusion planned over 2 weeks with for every center 1 week of classic information and 1 week of targeted information, allowing a randomized comparison of the 2 methods. To limit the biases of inclusions and the effect centers, every center will realize 1 week of every method, according to a specific drawing lots in every center to determine with which information (classic or targeted) the study will begin.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
February 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
French Cardiology Society
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • hospitalisation for scheduled coronarography

Exclusion Criteria

  • Coronarographies with general anesthesia.
  • Patients not speaking or not reading French, or having linguistic knowledge not allowing the delivery of an appropriate information

Outcomes

Primary Outcomes

Improvement of the quality of the information of the patients

Time Frame: one day

Improvement of the quality of the information of the patients by a video about the coronarography (realization of the procedure, the profits and the risks) associated with a written information. The quality of the information will be estimated by a dedicated score.

Study Sites (40)

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