Main
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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:
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IRCT |
Last refreshed on:
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22 February 2018 |
Main ID: |
IRCT2014121413156N10 |
Date of registration:
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2016-10-04 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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The impact of family-based education on the hope of Heart failure patients
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Scientific title:
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The impact of family-based education on the hope of Heart failure patients |
Date of first enrolment:
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2016-04-13 |
Target sample size:
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110 |
Recruitment status: |
Complete |
URL:
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http://en.irct.ir/trial/13086 |
Study type:
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interventional |
Study design:
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Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Supportive, Other design features: Table of random numbers.
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Phase:
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2
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Countries of recruitment
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Iran (Islamic Republic of)
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Contacts
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Name:
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Aleme Ghajar
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Address:
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Sari, Imam Sq, Joybar 3way, Start of valiye asr highway, Mazandaran University of Medical Sciences
Sari
Iran (Islamic Republic of) |
Telephone:
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+98 11 3336 7342 |
Email:
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aleme.ghajar@gmail.com |
Affiliation:
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Faculty of Nursing and Midwifery, Mazandaran University of Medical Sciences |
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Name:
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Mohammad Ali Heydarigorji
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Address:
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Sari, Imam Sq, Joybar 3way, Start of valiye asr highway, Mazandaran University of Medical Sciences
Sari
Iran (Islamic Republic of) |
Telephone:
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+98 11 3336 7342 |
Email:
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heydarigorji@yahoo.com |
Affiliation:
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Faculty member of Nursing and Midwifery |
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Key inclusion & exclusion criteria
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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
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Health Condition(s) or Problem(s) studied
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Cardiac, heart or myocardial failure NOS
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Heart failure. Cardiac, heart or myocardial failure NOS
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Intervention(s)
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In the control group, common training in hospital will receive.
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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.
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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.
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Behavior
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Primary Outcome(s)
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Hope. Timepoint: Before the intervention, three months after the intervention. Method of measurement: Miller hopes questionnaire.
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Secondary Outcome(s)
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-. Timepoint: -. Method of measurement: -.
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Source(s) of Monetary Support
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Vice Chancellor for Research of Mazandaran University of Medical Sciences
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Ethics review
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Status: Approved
Approval date:
Contact:
Ethics Committee of Mazandaran University of Medical Sciences
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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