Determine the effectiveness of the educational program based on the health belief model on the prevention behaviors of cardiovascular disease and hospital nursing staff.
Design
This study will be done on 104 people who will be randomly assigned to two groups of intervention and control.
Settings and conduct
The statistical population of this study is 104 nursing staff, staffs of operating room and anesthesia department at Koohdasht Imam Hospital in Lorestan in 2017.
Participants/Inclusion and exclusion criteria
Sample Entry Criteria:
All nursing staff, operating room and anesthesiologists working in Imam Khomeini Hospital in Koohdasht
Exit Sample Criteria:
History of cardiovascular disease
Participate in similar courses
Intervention groups
Intervention group: Determining the training needs after pre-test, develop a syllabus and educational content tailored to their needs, and training in 6 sessions of 40-30 minutes for 6 weeks. Control group: Without any intervention, the pretest and the test post are taken with the time interval of one month.
Main outcome variables
Scores obtained in all health belief model education structures
General information
Reason for update
Acronym
IRCT registration information
IRCT registration number:IRCT20171023036955N2
Registration date:2018-09-02, 1397/06/11
Registration timing:retrospective
Last update:2018-09-02, 1397/06/11
Update count:0
Registration date
2018-09-02, 1397/06/11
Registrant information
Name
Name of organization / entity
Country
Iran (Islamic Republic of)
Phone
+98 66 3263 0716
Email address
malekshahi@lums.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2017-11-11, 1396/08/20
Expected recruitment end date
2017-11-21, 1396/08/30
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
The effect of educational program based on health belief model on preventive behaviors of cardiovascular disease in Nurses
Public title
the effect of education on preventive behaviors of cardiovascular disease
Purpose
Prevention
Inclusion/Exclusion criteria
Inclusion criteria:
All nursing staff , operating room and staff working at the Imam khomeini hospital kuhdasht ( rah )
Exclusion criteria:
History of cardiovascular disease
participation in the same period
Age
No age limit
Gender
Both
Phase
N/A
Groups that have been masked
No information
Sample size
Target sample size:
104
Randomization (investigator's opinion)
Randomized
Randomization description
the present study is a randomized controlled trial. the study population consisted of 104 people from nursing staff operating theatre and anesthetics hospital Imam ( rah ) in the kuhdasht of lorestan 2017. individuals have been studied based on entry criteria and are randomly assigned to two groups according to the stratified random sampling method based on the work experience and the level of education
Blinding (investigator's opinion)
Not blinded
Blinding description
Placebo
Not used
Assignment
Other
Other design features
Secondary Ids
empty
Ethics committees
1
Ethics committee
Name of ethics committee
Ethics Committee in Lorestan University of Medical Sciences
Street address
Mediacl Campus, Khorramabad school of Medicine, 5th km of Borujerd-Kamalvand Road
City
Khorramabad
Province
Lorestan
Postal code
6813833946
Approval date
2017-09-11, 1396/06/20
Ethics committee reference number
IR.LUMS.REC.1396.298
Health conditions studied
1
Description of health condition studied
Cardiovascular diseases
ICD-10 code
...
ICD-10 code description
.....
Primary outcomes
1
Description
Preventive Behaviors of Cardiovascular Diseases
Timepoint
1 and 60 days after training
Method of measurement
Questionnaire
Secondary outcomes
empty
Intervention groups
1
Description
Intervention group: By obtaining information about the status of the participants and determining their educational needs, a training program with educational content tailored to their needs will be delivered to the participants through 6 30-40 minute sessions for 6 weeks
Category
Prevention
2
Description
Control group: Without any intervention, the pretest and the post test are taken with the time interval of one month.