How classroom indoor air affects children's allergies and wellbeing
Official title: Disrupting Noxious Synergies of Indoor Air Pollutants and Their Impact in Childhood Health and Wellbeing, Using Advanced Intelligent Multisensing and Green Interventions: an Interventional Study in a Sub-group of Schoolchildren
Run by University Hospital, Montpellier · NCT07402200 · Data updated 2026-11-12
This project will test whether continuous classroom and home air pollutant monitoring can identify pollution patterns linked to worse allergy or asthma symptoms in school-age children.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 8 Years to 12 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | University Hospital, Montpellier Academic / other |
| Locations | 1 site (Montpellier) |
| Status | Recruiting |
| Started | February 4, 2026 |
| Main results expected | June 2026 |
| Study ends | June 2026 |
| Registry record updated | February 11, 2026 |
| Trial ID | NCT07402200 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
School-aged children already enrolled in the SynAir-G observational study whose parents or guardians provide written informed consent, especially those with a history of allergic disease or asthma, are ideal candidates.
✕Probably not a fit
Children not enrolled in SynAir-G, those unable to comply with follow-up visits or sensor monitoring, and children without allergic or asthmatic symptoms may derive little direct benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Researchers will enroll children already in the SynAir-G observational cohort and classify them as cases or controls based on baseline questionnaire responses about asthma and allergic symptoms. Participants and caregivers will complete standardized questionnaires while children undergo skin prick allergy tests, non-invasive lung function tests, oxygen saturation checks, and provide biological samples as appropriate. Portable sensors placed in classrooms (and optionally at home) will continuously measure multiple air and dust pollutants to create individualized exposure baselines and detect changes over time. Health outcomes including respiratory symptoms, immune markers, and quality-of-life measures will be compared to the continuous exposure data to identify pollutant patterns associated with worsening or improvement.
Why it matters
Potential benefit: If successful, this approach could enable earlier detection of harmful exposures and targeted actions to reduce pollutants and improve allergy and asthma control in affected children.
How similar studies have gone: Prior studies have linked air pollution to worsened asthma and allergy outcomes, but the use of continuous, individualized classroom and home sensor data to link pollutant patterns to individual health outcomes is relatively novel and not yet widely proven.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Child included in the SynAir-G observational study * Child and caregiver(s) willing to follow the study procedures * Written informed consent from the child's parents/guardians * For case group, at least one positive answer (yes) to any of the following questions and for control group, negative answers to all the following questions based on the baseline questionnaire administered in the SynAir-G observational study, as shown below.: a. General health i. Does your child have any health problems (if yes to asthma, allergic rhinitis /rhino-conjunctivitis, atopic dermatitis)? b. Asthma i. Has your child ever had wheezing or whistling in the chest in the past 12 months? ii. In the past 12 months, has your child's chest sounded wheezy during or after exercise? iii. In the past 12 months, has your child had a dry cough at night, apart from a cough associated with a cold or chest infection? c. Rhinitis i. In the past 12 months has your child had a problem with sneezing, or a runny, or blocked nose when she/he DID NOT have a cold or the flu? d. Eczema (both answers yes) i. Has your child had this itchy rash at any time in the past 12 months? If so, has this itchy rash at any time affected any of the following places: the folds of the elbows, behind the knees, in front of the ankles, under the buttocks, or around the neck, ears or eyes? e. Food allergy i. Has your child had diagnosed food allergy during last 12 months? * For case group: Diagnosis of asthma/allergic rhinitis/eczema/food allergy (based on SYNAIR-G baseline questionnaire), active during the past year. * For control group: absence of diagnosis of asthma/allergic rhinitis/eczema/food allergy (based on SYNAIR-G baseline questionnaire) Exclusion Criteria: * Child or child's parents/guardians who: 1. Refuse to participate in the project / to give informed consent. 2. Do not want to follow the protocol procedures. 3. Do not read or/and write in French. 4. Plan a long stay outside the region that does not allow them to follow the visit plan. 5. The child is not affiliated to the French social security service
Where it's running
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CHU Montpellier
Montpellier, France Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.