Essential (primary) hypertension. Essential (primary) hypertension
Conditions
Interventions
Intervention 1: 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 consent will be fil
Lifestyle
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 consent will be filled out. If they
75 patients will be in control group. The control group won't participate in education sessions. The control group will receive routine education based on health centers program according to natio
Sponsors
Isfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
30 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: being interested to participate in the study; being middle-aged (65-30 years old); use drug for treatment of hypertension; the duration of diagnosed hypertension occurred at least for 6 months; not being involved in other common educational program related to hypertension at the same time and at least be literate. Exclusion criteria: the people don't want to continue the cooperation; participants who have attended at least two training sessions.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 months are evaluated. Method of measurement: (mmHg)measured by Mercury sphygmomanometer.;BMI. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 months are evaluated. Method of measurement: calibrated scale and meter.;Nutritional status. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 months are evaluated. Method of measurement: questionnaire.;Fatigue. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 months are evaluated. Method of measurement: fatigue visual basic.;Pain. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 months are evaluated. Method of measurement: pain visual basic.;Physical activity. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 months are evaluated. Method of measurement: questionnaire.;Depression. Timepoint: All variables at baseline, 1.5 month latter, and then at the end of 6 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 6 months are evaluated. Method of measurement: labratory kits. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: At the begining and 6 months later. Method of measurement: Questionnair QOL36 questions that validited among Iranian. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyde Shahrbanoo Daniali
Department of health education & health promotion School of health Isfahan University of Medical Sci
Outcome results
None listed