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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: IRCT
Last refreshed on: 22 February 2018
Main ID:  IRCT2014121413156N10
Date of registration: 2016-10-04
Prospective Registration: No
Primary sponsor: Vice Chancellor for Research of Mazandaran University of Medical Sciences
Public title: The impact of family-based education on the hope of Heart failure patients
Scientific title: The impact of family-based education on the hope of Heart failure patients
Date of first enrolment: 2016-04-13
Target sample size: 110
Recruitment status: Complete
URL:  http://en.irct.ir/trial/13086
Study type:  interventional
Study design:  Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Other design features: Table of random numbers.  
Phase:  2
Countries of recruitment
Iran (Islamic Republic of)
Contacts
Name: Aleme Ghajar   
Address:  Sari, Imam Sq, Joybar 3way, Start of valiye asr highway, Mazandaran University of Medical Sciences Sari Iran (Islamic Republic of)
Telephone: +98 11 3336 7342
Email: aleme.ghajar@gmail.com
Affiliation:  Faculty of Nursing and Midwifery, Mazandaran University of Medical Sciences
Name: Mohammad Ali Heydarigorji   
Address:  Sari, Imam Sq, Joybar 3way, Start of valiye asr highway, Mazandaran University of Medical Sciences Sari Iran (Islamic Republic of)
Telephone: +98 11 3336 7342
Email: heydarigorji@yahoo.com
Affiliation:  Faculty member of Nursing and Midwifery
Key inclusion & exclusion criteria
Inclusion criteria: Inclusion criteria:The minimum age of the patient should be 20 and maximum age is 80 years old? the doctor should confirm the disease diagnosis? Patients with class II and III heart failure? The patient or one of his family members should be understand Persian language?The patient should be consciousness? The exclusion criteria: the patient and his family do not want to cooperate anymore? The patient and his family have attended other organizations’ formal training.
Exclusion criteria:

Age minimum: 20 years
Age maximum: 80 years
Gender: Both
Health Condition(s) or Problem(s) studied
Cardiac, heart or myocardial failure NOS
Heart failure.
Cardiac, heart or myocardial failure NOS
Intervention(s)
In the control group, common training in hospital will receive.
Intervention 1: The training course consists of three successive sessions with the patient and one of his family members in the test group and the formulated content would be taught in three 1-hour sessions in 3 successive days. The training content includes: Explain the importance of having information about the disease and its complications and the importance of medication, medication use, diet, physical activity (first session); Limits of fluid intake, weight control, how to control vital signs, the importance of vaccinations and smoking cessation (second session); Ways to deal with hopelessness and depression, and Increasing hope and getting to know disease-causing symptoms and relapse (third session). Afterwards, phone follow up would continue every two weeks. In order to compare the test and control groups after three months, the effect of training course on quality of life will be investigated through posttest. Intervention 2: In the control group, common training in hospital will receive.
The training course consists of three successive sessions with the patient and one of his family members in the test group and the formulated content would be taught in three 1-hour sessions in 3 successive days. The training content includes: Explain the importance of having information about the disease and its complications and the importance of medication, medication use, diet, physical activity (first session); Limits of fluid intake, weight control, how to control vital signs, the importance of vaccinations and smoking cessation (second session); Ways to deal with hopelessness and depression, and Increasing hope and getting to know disease-causing symptoms and relapse (third session). Afterwards, phone follow up would continue every two weeks. In order to compare the test and control groups after three months, the effect of training course on quality of life will be investigated through posttest.
Behavior
Primary Outcome(s)
Hope. Timepoint: Before the intervention, three months after the intervention. Method of measurement: Miller hopes questionnaire.
Secondary Outcome(s)
-. Timepoint: -. Method of measurement: -.
Secondary ID(s)
Source(s) of Monetary Support
Vice Chancellor for Research of Mazandaran University of Medical Sciences
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
Ethics Committee of Mazandaran University of Medical Sciences
Results
Results available:
Date Posted:
Date Completed:
URL:
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