- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03791632
Oral Health Among Children (OHAC)
Oral Health Knowledge and Practice Among 8-9 Years Old Children.
The aim of this study is to identify the knowledge and behavior on dental health and hygiene among adolescents. In most cases, the investigators know tooth decay can be prevented and reversed at an early stage by observing good oral hygiene. Few studies have been done among adolescents.
This study could justify the implementation of public health actions in terms of prevention.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Montpellier, France, 34295
- UHMontpellier
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
- All children of classrooms selectionned
Exclusion criteria:
- Children absent on the day of the intervention
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: witness
2 control CE2 classes without oral sensitization actions
|
|
|
Experimental: group intervention 1
2 CE2 classes with a classical lecture style presentation
|
classical lecture style presentation
|
|
Experimental: group intervention 2
2 CE2 classes with an intervention in the form of fun workshops on different themes by small groups of schoolchildren (8-10 children per workshop)
|
an intervention in the form of fun workshops on different themes by small groups of schoolchildren (8-10 children per workshop)
|
|
Experimental: group intervention 3
2 CE2 classes with digital media intervention
|
digital media intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
comparison of children's notes before and after a prevention intervention
Time Frame: 1 day
|
The main result will be calculated with the total score to the questions. Each question corresponds to a point. The minimum score is 0 and the maximum score is 25. We will compare the evolution of the averages obtained by the control group and by all three other groups with Student test |
1 day
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compare the evolution of children's grades according to the type of intervention
Time Frame: before and after the explanation as well as one month and 6 months after the intervention
|
For the secondary objective, we will compare the evolution of the averages obtained between the three groups with intervention with ANOVA test. Each question corresponds to a point. The minimum score is 0 and the maximum score is 25. before and after the explanation as well as one month and 6 months after the intervention |
before and after the explanation as well as one month and 6 months after the intervention
|
|
Determine the timeframe by which children forget the information they have been given
Time Frame: before and after the explanation as well as one month and 6 months after the intervention
|
A questionnaire to know the oral knowledge will be distributed to the children before and after the explanation as well as one month and 6 months after the intervention
|
before and after the explanation as well as one month and 6 months after the intervention
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Camille INQUIMBERT, PhD student, University Hospital, Montpellier
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Other Study ID Numbers
- RECHMPL18_0386
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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