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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:  ACTRN12616000135415
Date of registration: 05/02/2016
Prospective Registration: Yes
Primary sponsor: Western Sydney University
Public title: Health literacy following an educational intervention in older Australians
Scientific title: Can an educational intervention improve health literacy and decision making about supporting self-advice and decision making among older Australians: a randomised controlled trial
Date of first enrolment: 01/08/2016
Target sample size: 168
Recruitment status: Completed
URL:  https://anzctr.org.au/ACTRN12616000135415.aspx
Study type:  Interventional
Study design:  Purpose: Educational / counselling / training; Allocation: Randomised controlled trial; Masking: Open (masking not used);Assignment: Parallel;Type of endpoint: Efficacy;  
Phase:  Not Applicable
Countries of recruitment
Australia
Contacts
Name: Prof Caroline Smith   
Address:  NICM Western Sydney University Locked Bag 1797 Penrith NSW 2751 Australia
Telephone: +61246203777
Email: caroline.smith@westernsydney.edu.au
Affiliation: 
Name: Prof Caroline Smith   
Address:  NICM Western Sydney University Locked Bag 1797 Penrith NSW 2751 Australia
Telephone: +61246203777
Email: caroline.smith@westernsydney.edu.au
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: men and women aged greater than 65 years, living in the Greater Western Sydney Region, and the Southern Highlands, New South Wales
Exclusion criteria: unable to communicate in English, living in a long term care facility

Age minimum: 65 Years
Age maximum: No limit
Gender: Both males and females
Health Condition(s) or Problem(s) studied
Alternative and Complementary Medicine - Other alternative and complementary medicine
healthy volunteers;
healthy volunteers
Intervention(s)
Health education.
Participants will be invited to watch the three module intervention in their home accessing the web link by a password protected code, or CD ROM over three weeks. The hardware required to use the education intervention will be by internet access, or for those using CD ROM a television or DVD player. Users will be able to pace their learning with back, next, end, replay, pause and play buttons. The duration of teaching module will be 30 minutes. Participants are able to access the intervention as often as they wish.
The content of the intervention will comprise of three modules and include materials and resources to inform the consumer about where to identify and obtain reliable information and credible sources of information about complementary medicines (CM), appraisal of health information, ability to find good information, and navigating the CM healthcare system. Information will be presented online using an education delivery package, and a video with a voice over.
Participants will be invited to read the three modules. One module involves interactive completion of questions using a multiple choice format.
Data will be collected from the web based intervention that document the length of time the web resource was used, and the number of times accessed.
Primary Outcome(s)
Complementary medicine decision self-efficacy using the Preparation for Decision Making Scale[3 weeks and 2 months after the intervention starts]
Secondary Outcome(s)
Health seeking behaviour assessed by practical follow up use of the resources presented. This will be assessed by self report from participants in response to questions designed specifically for the study [3 weeks and 2 months after the intervention starts]
health literacy using the Health Literacy Questionnaire[3 weeks and 2 months after the intervention starts]
change in perception of risk measured by two questions examining views on the safety and efficacy designed specifically for the study.[3 weeks and 2 months after the intervention starts]
knowledge assessed by presentation of a vignette to study participants, and their responses assessed by study staff.[3 weeks and 2 months after the intervention starts]
Secondary ID(s)
None
Source(s) of Monetary Support
IRT Foundation
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date:
Contact:
University of Notre Dame
Status: Approved
Approval date:
Contact:
University of Western Sydney
Results
Results available:
Date Posted:
Date Completed:
URL:
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