Primary blood pressure. Essential (primary) hypertension
Conditions
Interventions
Intervention 1: Intervention group: After registration of patients who want to participate in research projects. The goals and the process of research will be explained to them. Patient's informed con
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
40 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients have the ability to read and write At least 6 months have been diagnosed with early onset and ongoing treatment They are being treated for high blood pressure Failure to participate in a co-effective study on study variables Having the right physical conditions to attend training sessions Ability to answer the phone Suffering Primary blood pressure Being Healthy Psychological Did not have history of CVA and MI Not having chronic diseases affecting quality of life All patients are under the supervision of a doctor
Exclusion criteria
Exclusion criteria: Get extensive information about managing blood pressure from other sources or changing the treatment protocol Significant acute abnormalities and severe blood pressure or crisis Patient death
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: All variables at baseline and at the end of 3 months are evaluated. Method of measurement: Manometer.;BMI. Timepoint: All variables at baseline and at the end of 3 months are evaluated. Method of measurement: Calibrated scale and meter.;Nutritional status. Timepoint: All variables at baseline and at the end of 3 months are evaluated. Method of measurement: Questionnaire.;Physical activity. Timepoint: All variables at baseline and then at the end of 3 months are evaluated. Method of measurement: Questionnaire.;Paraclinic (Blood)tests: TG, cholestrol, Na of urine(24 hours). Timepoint: At baseline and at the end of 3 months are evaluated. Method of measurement: Labratory kits. | — |
Secondary
| Measure | Time frame |
|---|---|
| Self-management behaviors. Timepoint: At the beginning of the study and 3 months after the study. Method of measurement: Likert questionnaire.;Self-care behaviors. Timepoint: At the beginning of the study and 3 months after the study. Method of measurement: Likert questionnaire.;Self-regulation behaviors. Timepoint: At the beginning of the study and 3 months after the study. Method of measurement: Likert questionnaire.;Self-monitoring behaviors. Timepoint: At the beginning of the study and 3 months after the study. Method of measurement: Likert questionnaire.;Response to the disease. Timepoint: At the beginning of the study and 3 months after the study. Method of measurement: Likert questionnaire.;Training EASE program. Timepoint: During the 3 months of intervention. Method of measurement: Not. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contact???? ?????
Hamedan University of Medical Sciences
Outcome results
None listed