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Clinical Trials/IRCT2015100624395N1
IRCT2015100624395N1
Completed
未知

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

Vice chancellor for research, Mashhad University of Medical Sciences0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Valvular heart disease.
Sponsor
Vice chancellor for research, Mashhad University of Medical Sciences
Enrollment
60
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Vice chancellor for research, Mashhad University of Medical Sciences

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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