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ClimAIr: AI to Assess the Impact of Pollution and Climate on Respiratory Health in Europe

Climate Change and Air Contamination: Artificial Intelligence Applied on the Correlation Between Air Pollutants and Non-communicable Respiratory Diseases in Europe (ClimAIr)

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07107009
Acronym
ClimAIr
Enrollment
1906
Registered
2025-08-06
Start date
2026-01-31
Completion date
2027-12-31
Last updated
2025-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic Rhinitis, Asthma

Keywords

Air contamination, Air pollutants, Non-communicable respiratory diseases, Climate change, ClimAIr

Brief summary

The ClimAIr project will expand the evidence-based understanding of climate change, air pollution, and non-communicable respiratory diseases by using Artificial Intelligence (AI) tools. It will gather data on greenhouse gases levels and disaster risks, information on serious air pollutants and respiratory diseases' prevalence. The AI powered tools will be employed to generate better intervention methods and improve public health outcomes. Federated Learning (FL) will be used to develop AI models to protect patients' privacy. By raising public awareness and delivering the ClimAIr tool - specifically designed to health workers, urban planners and policy makers - the project aims to influence policy decisions, promote healthier environments, and reduce respiratory diseases in Europe, which will be tested and validated the ClimAIr tool in specific municipalities that are part of the project. ClimAIr draws on a consortium of 21 partners from 15 European countries, including carefully selected health centres across Europe - in Spain, Luxembourg, Ukraine, Italy, France, Germany, Greece, Romania and Poland - focused on respiratory diseases, which will provide disease data and explore metabolic routes of the studied contaminants/diseases. ClimAIr is composed of an interdisciplinary team formed by research centres, ethical AI and modelling experts, SSH specialists, municipal governance, and a Communication & Dissemination (C&D) expert team dedicated to achieving and spread the results of the project.

Interventions

None listed

Sponsors

Theramed Healthcare SRL (Romania)
CollaboratorUNKNOWN
Centre Hospitalier Universitaire de Toulouse, FRANCE
CollaboratorUNKNOWN
Charite-Universitaetsmedizin Berlin (Germany)
CollaboratorUNKNOWN
Aristotelio Panepistimio Thessalonikis (Greece)
CollaboratorUNKNOWN
Uniwersytet Medyczny w Lodzi (Poland)
CollaboratorUNKNOWN
Universita degli Studi di Milano (Italy)
CollaboratorUNKNOWN
Bukovinian State Medical University (Ukraine)
CollaboratorUNKNOWN
Luxembourg Institute of Health (Luxembourg)
CollaboratorUNKNOWN
Andaluz Health Service
CollaboratorOTHER_GOV
Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients with health insurance based in Malaga, Milan, Luxembourg, Thessalonikki, Lodz, Berlin, Toulousse, Chervnivtsi and Brasov (the places where environmental/climate information will be obtained from, only one recruitment place for partner). 2. 3-year history of chronic rhinitis symptoms during the corresponding pollen season, while residing in the same household AND attending the same school/college or holding the same job position. 3. Positive SPT and serum allergen-specific IgE \>0.35 kUA/L. The pollen species driving the nasal symptoms will be Olea europaea, Phleum pratense or Betula pendula. 4. Patients can be sensitized to other aeroallergens if the nasal symptoms occur exclusively or aggravate unequivocally during the pollen season of the three allergens of interest.

Exclusion criteria

Lack of reliable information in e-health records, allergen immunotherapy (any allergen) during the previous 5 years, systemic immunosuppressants or biologicals in the previous six months, chronic rhinosinusitis, and severe systemic conditions.

Design outcomes

Primary

MeasureTime frameDescription
Mean Symptom Score of Allergic Rhinitis Patients by Environmental ExposureRetrospective data collected over a 3-year period prior to study enrollment.Mean allergic rhinitis symptom scores retrieved from electronic health records (EHR), stratified by environmental exposure levels (pollutants and climate factors), using the Observational Medical Outcomes Partnership (OMOP) common data model.
Proteomic Biomarker Levels (NPX) by Environmental ExposureSamples collected prospectively between months 10 and 15 (October-March, out-of-pollen season).Proteomic profiles measured using Olink® assays in serum and nasal lavage of allergic rhinitis patients, stratified by environmental exposure.

Secondary

MeasureTime frameDescription
SO1: Effect of air pollution on adaptive immune responses to allergenic pollenSample collection and analysis performed prospectively between months 10 and 24.Evaluation of the immune response of peripheral blood mononuclear cells (PBMCs) from allergic rhinitis patients exposed to different environmental conditions, after in vitro stimulation with pollen samples previously exposed to varying pollution levels. The response will be characterized by proliferation of allergen-specific lymphocyte subsets and cytokine production.
SO1: Proliferative responses of allergen-specific lymphocytes to pollen exposed to pollutionAssays conducted on samples collected between months 10 and 24.Measurement of lymphocyte proliferation using CFSE-labeled PBMCs incubated with pollen (Olea europaea, Phleum pratense, Betula pendula) grown under different pollution conditions.
SO1: Cytokine release from allergen-specific lymphocytes in response to polluted pollenAnalysis performed between months 10 and 24, post-sample collection.Quantification of cytokines released in the supernatants of PBMC cultures stimulated with pollen under different pollution conditions. A multiplex ELISA panel will be used to measure Th1, Th2, Th9, and regulatory cytokine

Contacts

Primary ContactIbon Eguiluz Gracia, MD, PhD
iboneguiluz@gmail.com+34 951 291 073

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026