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The effect of education based on the family-centered empowerment model on anticoagulant adherence of patients with prosthetic heart valve.

Not Applicable
Conditions
Valvular heart disease.
Endocarditis and Heart valve Disorders in Diseases Classified Elsewhere
Registration Number
IRCT2015100624395N1
Lead Sponsor
Vice chancellor for research, Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Willingness to participate in the study ; The age range of 65- 18 years; living in Mashhad; Artificial valve replacement surgery;The first shift valve replacement surgery; Failure to develop an advanced chronic disease (stroke, kidney failure) and lack cognitive and mental disorders (Alzheimer's, depression); Loss of speech and hearing problems; Having read and write; The patient has no health personnel; A family member (spouse, child, sister, etc.) that further cooperation in the field of health -care and the patient is Family members living with the patient; Lack of family members to valve disease

Inclusion criteria 10,11 and 12 will be considered for patients in the intervention group.

Inclusion criteria of active member of the family: willingness to participate in research; having read and write; lack of drug addiction; without the risk of heart valve disease; Is not of Health care worker

Exclusion criteria: unwillingness of research or a member of his family to cooperate at every stage of research; hospitalization for any reason at any stage of research; changes in the anticoagulant medication; The incidence of postoperative complications requiring surgery, physical or mental problems that lead to disability at any stage of the research.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Adherence to anticoagulant treatment regimen. Timepoint: one and half month after intervention. Method of measurement: Questionnaire of Adherence to anticoagulant treatment regimen.
Secondary Outcome Measures
NameTimeMethod
Bleeding. Timepoint: Three months after intervention. Method of measurement: Landfield questionnaire.
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