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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: ANZCTR
Last refreshed on: 13 January 2020
Main ID:  ACTRN12616001699459
Date of registration: 09/12/2016
Prospective Registration: Yes
Primary sponsor: Samia Amin
Public title: Effectiveness of educational intervention on knowledge, belief and self-efficacy regarding osteoporosis among the female academic staff in Universiti Putra Malaysia
Scientific title: Effectiveness of educational intervention on knowledge, belief and self-efficacy regarding osteoporosis among the female academic staff in Universiti Putra Malaysia
Date of first enrolment: 01/01/2017
Target sample size: 240
Recruitment status: Not yet recruiting
URL:  https://anzctr.org.au/ACTRN12616001699459.aspx
Study type:  Interventional
Study design:  Purpose: Educational / counselling / training; Allocation: Randomised controlled trial; Masking: Blinded (masking used);Assignment: Parallel;Type of endpoint: Efficacy;  
Phase:  Not Applicable
Countries of recruitment
Malaysia
Contacts
Name: Dr Samia Amin   
Address:  Department of community medicine,Faculty of Medicine and Health science,Universiti Putra Malaysia,Jalan Upm, 43400 Serdang, Selangor, Malaysia Malaysia
Telephone: +60142996859
Email: drsamia27@gmail.com
Affiliation: 
Name: Dr Samia Amin   
Address:  Department of community medicine,Faculty of Medicine and Health science,Universiti Putra Malaysia,Jalan Upm, 43400 Serdang, Selangor, Malaysia Malaysia
Telephone: +60142996859
Email: drsamia27@gmail.com
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: i. Female academic participants are working as a full time staff in UPM.
ii. Female academic participants age in between 25-55 years.
iii. Female academic participants with English language
iv. Female academic participants will give written consent.
v. Female academic participants will not going for leave in coming three months.
vi. Female academic participants are using smart mobile phone with internet subscription.

Exclusion criteria: i. Female academic participants diagnosed as osteoporosis.
ii. Female academic participants come for short time training
iii. Pregnant Female academic participants
iv. Female academic participants has chronic disease with medication (e.g. Hypertension/Diabetics)
v. Active female academic participant in another study.
vi. Female academic doctor and nurse staff


Age minimum: 25 Years
Age maximum: 55 Years
Gender: Females
Health Condition(s) or Problem(s) studied
Knowledge, belief and self-efficacy regarding osteoporosis among the female academic staff in Universiti Putra Malaysia;
Knowledge, belief and self-efficacy regarding osteoporosis among the female academic staff in Universiti Putra Malaysia
Musculoskeletal - Osteoporosis
Public Health - Health promotion/education
Intervention(s)
*The study will be conducted among the female staff in Universiti Putra Malaysia, Serdang. According to university website (www.upm.edu.my; 2015) total female staff is about more than one thousand. Only academic female staff of this university will be included in this study.
* Respondents who meet the inclusion criteria will be taken as respondent by multi stage random sampling.
*There are sixteen different faculties in Universiti Putra Malaysia; eight different faculties will be allocated for each intervention and control group to achieve the sample size.
*Respondents for both intervention and control group will be single blinded to reduce bias. The respondent will not be informed whether they are categorized under intervention or control group. Only the researcher is able to differentiate which groups are under intervention or control group.
* The intervention group will receives information’s about osteoporosis by education material and control group will not receive any information’s related to osteoporosis. After the completion of the trial the control group will receive the educational material through email.
*Researcher herself will distribute the booklet (educational material) which will includes the information on development, risk, consequences and prevention strategies of osteoporosis among the intervention group.
*Educational material (booklet) develop under “Health Belief Model” will be prepared by principal investigator specifically highlight the study objectives by comprehensive literature review from previous studies.
*All participants will answer a set of validated and pretested questionnaire at baseline, immediately and three months after intervention.
*To reduce the noncompliance in the study the researcher will send weekl
Primary Outcome(s)
Osteoporosis belief assessed by questionnaire designed for this study [At baseline, immediately after intervention commencement and at 3 months after intervention commencement ]
Osteoporosis self-efficacy assessed by questionnaire designed for this study[At baseline, immediately after intervention commencement and at 3 months after intervention commencement ]
Osteoporosis knowledge assessed by questionnaire designed for this study [At baseline, immediately after intervention commencement and at 3 months after intervention commencement ]
Secondary Outcome(s)
Proportion of participants with an improve Osteoporosis Self-Efficacy Scale (OSES) [Immediately after intervention commencement and at 3 months after intervention commencement]
Proportion of participants with an improve Osteoporosis Health Belief Scale (OHBS).[Immediately after intervention commencement and at 3 months after intervention commencement]
Proportion of participants with an improve Osteoporosis Knowledge Test (OKT) score[Immediately after intervention commencement and at 3 months after intervention commencement]
Secondary ID(s)
Nil known
Source(s) of Monetary Support
Samia Amin
Secondary Sponsor(s)
Assoc. Prof. Dr. Hejar Abdul Rahman
Dr. Emilia Zainal Abidin
Dr. Suriani Ismail
Ethics review
Status: Approved
Approval date:
Contact:
JKEUPM (Ethic Committee For Research Involving Human Subject)
Results
Results available:
Date Posted:
Date Completed:
URL:
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