- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04475003
Health Literacy Among Caregivers of Children With IgE-mediated Allergy With Risk of Anaphylaxis
Research on health literacy among caregivers of children with IgE-mediated allergy at risk of anaphylaxis (life-threatening allergic reaction). Health literacy is a person's ability to understand health information so that they can maintain or improve their health and quality of life (of themself and children).
The aim of the study is to test the general knowledge of anaphylaxis. Furthermore we test the extent to which caregivers consider themselves able to recognize and to treat anaphylaxis.
Study Overview
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Jasmine S Leus
- Phone Number: +329 246 8200
- Email: jasmine.leus@azmmsj.be
Study Contact Backup
- Name: Josefien L Vandekerckhove
- Phone Number: +329 246 8200
- Email: josefien.vandekerckhove@gmail.com
Study Locations
-
-
Oost-Vlaanderen
-
Gent, Oost-Vlaanderen, Belgium, 9000
- Algemeen ziekenhuis Maria Middelares
-
Contact:
- Jasmine S Leus
- Phone Number: +329 246 8200
- Email: jasmine.leus@azmmsj.be
-
Contact:
- Josefien L Vandekerckhove
- Phone Number: +329 246 8200
- Email: josefien.vandekerckhove@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- caregivers of children with IgE-mediated allergy with risk of anaphylaxis (adults, grandparents, school caregivers etc.).
- minimum 18 years old.
- signed informed consent
Exclusion Criteria:
- none
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
General knowledge of anaphylaxis.
Time Frame: 1.5 year
|
Knowledge Quiz
|
1.5 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The extent to which caregivers consider themselves able to recognize and to treat anaphylaxis.
Time Frame: 1.5 year
|
Numeric scoring scale (0= cannot do at all, 5= highly certain can do)
|
1.5 year
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jasmine S Leus, Algemeen ziekenhuis Maria Middelares
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MMS2020.017
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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