Effectiveness of an educational intervention (the Encourage Autonomous Self-Enrichment Program) on self- management in Patients with high blood pressure

Not Applicable

Recruiting

• Conditions: Primary blood pressure.; Essential (primary) hypertension

• Registration Number: IRCT20170123032129N6
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 70

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

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.