Education Program for Patients Receiving Oral Anticoagulation

Status Recruiting

Clinical Trial Summary

The aim of the study is to test if patients under oral anticoagulation therapy who are going to participate in the education program will have better Health-related quality of life, higher rate in pharmacological treatment adherence and better self efficacy to manage the treatment.

Clinical Trial Description

Patients who are going to use oral anticoagulant will participate in an individual orientation, using instructional material (slides and illustrative booklet) during hospitalization period. After the discharge 2 phone calls will be done (after: a week and four weeks) focusing on the strategies to improve patient's self-efficacy to manage the oral anticoagulation. There will be a personal contact among researcher and participants when the patients return at the oral anticoagulant ambulatory, two months after the treatment start. At this time the following variables of interest will be evaluated: Health-related quality of life; adherence to treatment and patients' self-efficacy. ;

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01339611
Study type	Interventional
Source	University of Sao Paulo
Contact	Flávia M Pelegrino, MNS, PhD candidate
Phone	55-16-36023402
Email	flavia-martinelli@bol.com.br
Status	Recruiting
Phase	N/A
Start date	May 2011
Completion date	December 2012

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