- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05645120
Impact of Nutrition Education on Knowledge and Beliefs About Dietary Supplements/Herbal Foods
December 9, 2022 updated by: Zeynep Goktas, Hacettepe University
Impact of Nutrition Education on Knowledge and Beliefs About Dietary Supplements/Herbal Foods: A Pre - Post Intervention Study
A two session nutrition education intervention was administered to health professionals and non-health professionals in separate sessions.
Nutrition knowledge status was evaluated with comparing the pre-test and post-test values.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The purpose of this study is to evaluate the efficacy of nutrition education intervention of health professionals and non-health professionals about the effectiveness of dietary supplements/herbal foods (DS/HF) in COVID-19.
Study design is a cross-sectional study with an education intervention.
This study was conducted through online video communication application.
Overall, 106 health professionals and 110 non-health professionals completed the study.
The education intervention was administered in two sessions, one week apart for both health professionals and non-health professionals separately.
Knowledge level of nutrition and COVID-19 and beliefs about DS/HF in the prevention/treatment of COVID-19 were evaluated with a pre-test and post-test setting.
Comparison of the groups before and after the intervention was implemented with the McNemar's test.
Study Type
Interventional
Enrollment (Actual)
226
Phase
- Not Applicable
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
-
-
-
Ankara, Turkey, 06100
- Hacettepe University
-
-
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
19 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- being 18 to 65 years old
- using social media
- being able to understand Turkish
Exclusion Criteria:
- regular supplement use prior to COVID-19 pandemic
- having a chronic disease that requires dietary supplementation
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
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Health Professionals
Education intervention for health professionals
|
All participants attended to a two-part nutrition education program.
The education intervention program was administered in two sessions, one week apart.
Before the intervention, a pre-test was administered to determine the knowledge and beliefs attitudes of participants.
After the pre-test each session consisted of a PowerPoint presentation of about 20 minutes.
Education topics included components of adequate-balanced nutrition and its relationship with COVID-19, introduction of food groups, the association between COVID-19 and dietary supplements, herbal foods in the prevention/treatment of COVID-19, considerations regarding DS/HF, food-drug interactions, and COVID-19 drugs and food interactions.
The presentation was concluded with the nutritional recommendations for COVID-19.
The post-tests were shared with the participants at the end of the second session of the education intervention.
|
|
Experimental: Non-health Professionals
Education intervention for non-health professionals
|
All participants attended to a two-part nutrition education program.
The education intervention program was administered in two sessions, one week apart.
Before the intervention, a pre-test was administered to determine the knowledge and beliefs attitudes of participants.
After the pre-test each session consisted of a PowerPoint presentation of about 20 minutes.
Education topics included components of adequate-balanced nutrition and its relationship with COVID-19, introduction of food groups, the association between COVID-19 and dietary supplements, herbal foods in the prevention/treatment of COVID-19, considerations regarding DS/HF, food-drug interactions, and COVID-19 drugs and food interactions.
The presentation was concluded with the nutritional recommendations for COVID-19.
The post-tests were shared with the participants at the end of the second session of the education intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge Level
Time Frame: 2 weeks
|
Comparison of mean scores from pre-test and post-test
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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, 2021
Primary Completion (Actual)
December 30, 2021
Study Completion (Actual)
March 1, 2022
Study Registration Dates
First Submitted
December 1, 2022
First Submitted That Met QC Criteria
December 1, 2022
First Posted (Actual)
December 9, 2022
Study Record Updates
Last Update Posted (Estimate)
December 13, 2022
Last Update Submitted That Met QC Criteria
December 9, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- GO 21/129
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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