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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. |
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Register:
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IRCT |
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Last refreshed on:
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22 February 2018 |
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Main ID: |
IRCT2017010528863N10 |
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Date of registration:
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2017-06-19 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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use of vitamin D supplements Among Female High School Students
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Scientific title:
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The effect of education for use of vitamin D supplements based on the health belief model Among Female High School Students |
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Date of first enrolment:
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2016-01-20 |
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Target sample size:
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140 |
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Recruitment status: |
Complete |
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URL:
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http://en.irct.ir/trial/23317 |
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Study type:
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interventional |
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Study design:
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Randomization: Randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Prevention.
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Phase:
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N/A
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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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Dr nooshin peyman
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Address:
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School of Public Health
mashhad
Iran (Islamic Republic of) |
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Telephone:
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+98 35 1853 8530 |
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Email:
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peymann@mums.ac.ir |
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Affiliation:
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Mashhad University of Medical Sciences |
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Name:
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Dr nooshin peyman
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Address:
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School of Public Health
13944-91388
mashhad
Iran (Islamic Republic of) |
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Telephone:
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+853 8530 |
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Email:
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peymann@mums.ac.ir |
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Affiliation:
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mashhad University of Medical Sciences, Mashhad, Iran |
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Key inclusion & exclusion criteria
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Inclusion criteria: Inclusion criteria: 1- who agreed to participate; 2- Minimum age =15 years and maximum was 18
Exclusion criteria: They do not want to cooperate; absence of more than 1 in training sessions
Exclusion criteria:
Age minimum:
15 years
Age maximum:
18 years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Vitamin D deficiency.
Vitamin D deficiency, unspecified
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Vitamin D deficiency, unspecified
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Intervention(s)
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Intervention 1: The intervention group received educational content based on on the health belief model. Educational content based on predetermined objectives presented in 3 sessions(45-60 minutes during 3 weeks.). Intervention 2: The control group did not receive any training program.
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The intervention group received educational content based on on the health belief model. Educational content based on predetermined objectives presented in 3 sessions(45-60 minutes during 3 weeks.)
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The control group did not receive any training program.
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Primary Outcome(s)
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Use of vitamin D supplements. Timepoint: before, immediately and 3 month after intervention. Method of measurement: questionnaire.
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Secondary Outcome(s)
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Knowledge, perceived susceptibility, perceive severity, perceived barrier, perceived benefit, self-efficacy. Timepoint: before, immediately and 3 month after intervention. Method of measurement: questionnaire.
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Source(s) of Monetary Support
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Vice chancellor for research Mashhad University of Medical Sciences
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Ethics review
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Status: Approved
Approval date:
Contact:
Mashhad 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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