- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03561636
Health Literacy in the General Population in Belgium
April 23, 2019 updated by: Isabelle Bragard, University of Liege
Health Literacy in the General Population in Belgium: Associations and Determinants
The aims of the study are:
- To measure health literacy (HL) levels in a sample composed of members of a health mutual (Solidaris), and its potential associations with several determinants (health, health services consumption, health behaviours...)
- To identify potential groups at risk of a lower HL
- To identify the determinants of HL level
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
2535
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Liege, Belgium, B-4000
- University Hospital of Liege
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Liège, Belgium, 4000
- University of Liege
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Adults affiliated to Solidaris
Description
Inclusion Criteria:
- 18 years old or more
- Affiliated to Solidaris (health mutual), with a valid phone number
- Consent to participate
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Health Literacy
Time Frame: At the inclusion in the study
|
The degree to which individuals can obtain, process and understand basic health information and services needed to make appropriate health decisions.
It also includes the cognitive and social skills which determine the motivation and ability of individuals to gain access to, understand and use information in ways which promote and maintain good health.
It is measured by the Health Literacy Questionnaire (HLQ) (Osborne et al., 2013), composed of 44 items (9 dimensions).
|
At the inclusion in the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
General health
Time Frame: At the inclusion in the study
|
Measured with the EQ-5D-5L (EuroQol Group, 1990), divided into 2 parts.
The first part is composed of 5 items investigating 5 dimensions (mobility, autonomy, daily activities, pain, and anxiety and depression).
|
At the inclusion in the study
|
General health
Time Frame: At the inclusion in the study
|
Measured with the EQ-5D-5L (EuroQol Group, 1990), divided into 2 parts: the second part is composed of 1 Visual Analogue Scale (VAS, from 0 to 100), investigating the perceived health.
|
At the inclusion in the study
|
Chronic illnesses
Time Frame: At the inclusion in the study
|
Questions about the presence of chronic illness(es) are asked, along with their duration.
|
At the inclusion in the study
|
Body Mass Index
Time Frame: At the inclusion in the study
|
Calculated with the standard formula (weight/height²)
|
At the inclusion in the study
|
Feeling of stigma associated with the chronic illness
Time Frame: At the inclusion in the study
|
Measured with the Stigma Scale for Chronic Illnesses (Molina et al., 2013), which assesses enacted and internalised stigma.
It is composed of 8 items.
The responses for each item can be: 1 = Never, 2 = Rarely, 3 = Sometimes, 4 = Often, and 5 = Always.
The raw summed score range is 8-40, with a higher score indicating a higher perceived stigma.
Raw scores are then transformed into T-scores (a result of rescaling raw scores into standardized scores with a mean of 50 and a standard deviation of 10).
|
At the inclusion in the study
|
Satisfaction about health services
Time Frame: At the inclusion in the study
|
Investigation of the participant's satisfaction about hospitals, dentists, specialised physician, general practitioners, home care and Solidaris, through 6 questions ranging from 1 (very unsatisfied) to 5 (very satisfied).
|
At the inclusion in the study
|
Consumption behaviors
Time Frame: At the inclusion in the study
|
Tobacco, alcohol, fruits and vegetables consumption are investigated through 5 questions: do you smoke ?
/ If yes, what do you smoke?
/ How often do you drink alcohol?
/ How often do you eat fruits?
/ How often do you eat vegetables?
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At the inclusion in the study
|
Physical activity
Time Frame: At the inclusion in the study
|
Investigated through 2 questions: during the last 7 days, how many days did you practice intense physical activity?
/ during the last 7 days, how many days did you practice moderate physical activity?
For each question, answers range from 0 to 7.
|
At the inclusion in the study
|
Use of the Internet for health purposes
Time Frame: At the inclusion in the study
|
Investigated through 1 question: "how often do you use the Internet to search information about your health?".
Answers range from 1 (never) to 5 (always).
|
At the inclusion in the study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2017
Primary Completion (Actual)
June 30, 2018
Study Completion (Actual)
June 30, 2018
Study Registration Dates
First Submitted
May 23, 2018
First Submitted That Met QC Criteria
June 18, 2018
First Posted (Actual)
June 19, 2018
Study Record Updates
Last Update Posted (Actual)
April 24, 2019
Last Update Submitted That Met QC Criteria
April 23, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HL-Solidaris
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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