- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07359937
Design of a Multicomponent Intervention to Reduce the Risk of Exposure Fluorine
January 14, 2026 updated by: Universidad Antonio Nariño
Design of a Multicomponent Intervention to Reduce the Risk of Exposure to High Concentrations of Fluoride in Children in Huila, Colombia
Introduction Systemic exposure to fluoride is a significant challenge for global public health; this is because although fluoride prevents dental caries, prolonged exposure to high concentrations can cause adverse effects on various organs and systems, especially the teeth.
Despite the existence of preventive strategies to reduce this exposure, evidence on the effectiveness of multicomponent interventions is limited.
This protocol describes the design of a randomized controlled trial to evaluate the effects of a multicomponent intervention on parents and children to reduce the risk of exposure to high concentrations of fluoride in children.
Methods This is a randomized controlled trial, and kindergartens in the municipalities of the Department of Huila, Colombia, will be recruited.
The intervention group will receive a comprehensive five-component program: installation of water filters to reduce fluoride consumption; educational sessions for parents and children to raise awareness and promote healthy practices; outreach activities to strengthen collective knowledge; and a maintenance phase to ensure the program's sustainability.
In contrast, the control group will participate in a conventional educational strategy focused on the parent-child dyad.
Measurements will be taken at four points in time: pre-intervention for baseline and post-intervention at 3, 6, and 12 months.
The evaluation of results includes the concentration of fluoride in children's urine, fluoride levels in water (to validate the effectiveness of filtration), and changes in parents' knowledge, attitudes, and practices.
Discussion The trial will evaluate the effectiveness of a multicomponent intervention aimed at parents and children to reduce the risk of fluoride exposure.
Through integrative methodological approaches and objective measurements, it will demonstrate significant improvements in reducing fluoride exposure in children and in parents' knowledge, attitudes, and practices.
It will contribute to child health programs, strengthen preventive oral health strategies with an impact on public policy, community health, and new lines of research on fluoride.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
90
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
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Palermo, Colombia
- Centro de desarrollo infantil - Sonrisitas de oro
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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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Kindergartens located in municipalities with exposure to fluoride concentrations in water.
- Have a school feeding program.
- The child must be enrolled.
- They must be registered in the school feeding program.
- The primary caregiver must be able to read.
- The caregiver must agree to participate voluntarily and sign the informed consent form.
- The caregiver must commit to attending all components of the intervention (education and collection of the child's urine sample).
Exclusion Criteria:
- Parents or children with conditions or situations that may interfere with the assimilation of the components of the strategy.
- Children who wear diapers will be excluded from the study.
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Side
multicomponent intervention
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1. Installation of physical barriers: a reverse osmosis water filter.
2. Educational sessions for parents: three thematic modules.
3. Educational sessions for children: one thematic modules.
4. Outreach activities: To ensure the sustainability of the intervention.
5. Maintenance phase: The population will have free access to educational resources through the "Camaleón Sonriente cuida tus dientes" (Smiling Chameleon Takes Care of Your Teeth)
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Active Comparator: Control side
Conventional intervention
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The intervention will include training on the cariogenic diet, flossing, and hand washing.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Urinary fluoride concentrations
Time Frame: Time Frame: Baseline, 3 , 6, and 12 months.
|
Decrease in urinary fluoride concentrations in children
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Time Frame: Baseline, 3 , 6, and 12 months.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge, attitudes, and practices (KAP)
Time Frame: Time Frame: Baseline, 3 , 6 and 12 months.
|
To assess changes in parents' knowledge and attitudes, the Knowledge, Attitudes, and Practices (KAP) survey will be administered, after validation.
The instrument was designed for this purpose, taking into account the components of the intervention.
The knowledge section consists of 12 items and explores parents' understanding of natural and non-natural sources of fluoride and its effects on oral and systemic health.
The attitudes section consists of 10 items and identifies perceptions, beliefs, motivations, and willingness to act in response to fluoride risk, water quality, willingness to change habits, and dental follow-ups.
The practices section, with 9 items, addresses information on current behaviors related to consulting fluoride content, modifying water sources, dental care, and supervision in the use of dental products.
Each section of the instrument includes ordinal scale variables and provides an overall score that allows each section to be classified as good, fair, or poor.
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Time Frame: Baseline, 3 , 6 and 12 months.
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Fluoride concentrations in water
Time Frame: Time Frame: baseline, 3, 6, and 12 months
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Reduction in fluoride concentrations in water.
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Time Frame: baseline, 3, 6, and 12 months
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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)
August 1, 2025
Primary Completion (Estimated)
August 6, 2026
Study Completion (Estimated)
June 30, 2027
Study Registration Dates
First Submitted
January 14, 2026
First Submitted That Met QC Criteria
January 14, 2026
First Posted (Actual)
January 22, 2026
Study Record Updates
Last Update Posted (Actual)
January 22, 2026
Last Update Submitted That Met QC Criteria
January 14, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Dental Enamel Hypomineralization
- Developmental Defects of Enamel
- Stomatognathic Diseases
- Tooth Diseases
- Chemically-Induced Disorders
- Stomatognathic System Abnormalities
- Congenital Abnormalities
- Poisoning
- Tooth Abnormalities
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Behavior
- Treatment Adherence and Compliance
- Health Behavior
- Patient Compliance
- Patient Acceptance of Health Care
- Adherence Interventions
- Medication Adherence
- Fluorosis, Dental
- Fluoride Poisoning
- Health Education
Other Study ID Numbers
- UAN-Fluorine
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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