- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07678528
Exposome, Pollutants, Biology in the Older Subject: EXPOSAGE (EXPOSAGE)
24. juni 2026 oppdatert av: Centre Hospitalier Universitaire de Nice
Numerous factors, both individual and environmental, can influence aging, an individual's health, and their functional status.
However, the understanding of the combined impact of lifestyle-related exposures (e.g., physical activity, diet, sleep) (personal external exposome), exposures to pollutants (environmental external exposome), and their biological responses (internal exposome)-in other words, the impact of the "exposome" on healthy aging-remains limited, particularly in characterizing the molecular mechanisms associated with these interactions.
Exposome approaches identifying key exposures and molecular mechanisms could lead to a better understanding of how the environment, interacting with health behaviors, can affect functional status.
Thus, the objective of this study is i) to evaluate the links between the external exposome, the internal exposome and the health of older and aging individuals, and ii) to identify biological markers associated with a vulnerable health status in older and aging individuals.
Studieoversikt
Status
Har ikke rekruttert ennå
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
400
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Virginie PIOVANO
- E-post: piovano.v@chu-nice.fr
Studer Kontakt Backup
- Navn: Olivier GUERIN, PROFESSOR
- Telefonnummer: 0492034194
- E-post: guerin.o@chu-nice.fr
Studiesteder
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-
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Nice, Frankrike
- CHU de Nice - Hopital de Cimiez
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Hovedetterforsker:
- Olivier GUERIN, Pr
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Ta kontakt med:
- Olivier GUERIN, Pr
- Telefonnummer: 0492034194
- E-post: guerin.o@chu-nice.fr
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Ja
Beskrivelse
Inclusion Criteria:
- Aged 55 or over
- Affiliated with or beneficiaries of a social security scheme
- Signed the informed consent form •-Persons residing in one of the following municipalities : Antibes, Le Bar-sur-Loup, Berre-les-Alpes, Beuil, Blausasc, Breil-sur-Roya, Cabris, Cannes, Carros, Clans, Contes, Drap, L'Escarène, Escragnolles, Fontan, La Gaude, Gilette, Grasse, Lantosque, Levens, Nice, Peillon, Peymeinade, Saint-André-de-la-Roche, Saint-Etienne-de-Tinée, Sospel, Tourrettes-sur-Loup, Vence, Tende
Exclusion Criteria:
- patients currently undergoing intensive drug treatment, including chemotherapy
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Annen: Exposome assessment
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Visit 1: blood sample, questionnaires on the personal exposome (lifestyle habits (e.g., physical activity, diet, stress) and social characteristics and health status) | ii) Outpatient assessment: wearing a silicone bracelet for 7 days to measure external environmental exposure to pollutants and quantify physical activity | iii) Visit 2: 1-year follow-up of health status
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Frailty (health measure)
Tidsramme: at baseline and 12 months later
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Frailty is assessed using the Groningen Frailty Indicator.
The scale comprises 15 items.
The total score ranges from 0 to 25, with a higher score being worse.
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at baseline and 12 months later
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Functional and health status
Tidsramme: at baseline and 1 year
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Disease presence : : Presence (yes/no) of chronic disease
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at baseline and 1 year
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Physical functional capacities (health measure)
Tidsramme: at baseline and at 12 months
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Physical functional capacities are assessed using the Short Physical Performance Battery which assess balance, walking capacities and strength via a sit to stand test
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at baseline and at 12 months
|
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Quality of life (health measure)
Tidsramme: at baseline and 12 months
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Quality of life is assessed using the SF-12 questionnaire.
The scale comprises 12 items.
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at baseline and 12 months
|
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Autonomy (health measure)
Tidsramme: at baseline and 12 months
|
Autonomy is assessed using the WHOQOL-OLD-AUT questionnaire.
The scale comprises 4 items.
The total score ranges from 4 to 20, with a higher score being better.
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at baseline and 12 months
|
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Comorbidity (health measure)
Tidsramme: at baseline and 12 months
|
Comorbidity is assessed using the Charlson Index which counts the number of comorbidities.
Higher score means greater number of comorbidities and therefore a poorer health.
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at baseline and 12 months
|
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Pollutant metabolites (internal exposome/biological measure)
Tidsramme: at baseline.
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Presence in the blood metabolome of molecules directly associated with pollutants (initial or biotransformed compounds).
This outcome will be obtained through a metabolomic analysis by very high-resolution mass spectrometry (consisting of the analysis of all small organic molecules (or metabolites)) performed on blood samples taken by a blood sampling.
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at baseline.
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DNA and telomere damage (internal exposome/biological measure)
Tidsramme: at baseline.
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DNA damage will be obtained through epigenetic analysis by studying miRNAs.
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at baseline.
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exposure to air pollutants (external environmental exposome measure)
Tidsramme: at baseline
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characteristics in terms of air pollution of the living space (quantity of fine particulate matter (PM), ozone (O3), nitrogen dioxide (NO2), or sulfur dioxide (SO2))
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at baseline
|
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exposure to pesticides, hydrocarbons, plastics, flame retardant pollutants (external environmental exposome measure)
Tidsramme: at baseline
|
the exposure will be obtained through a silicone bracelet worn for 7 days by the participant, which will allow the measure of all exposures in the person's daily life.
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at baseline
|
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Smoking habits (external personal exposome measure)
Tidsramme: at baseline.
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smoking/non-smoking status identified via questionnaire.
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at baseline.
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Alcohol habits (external personal exposome measure)
Tidsramme: at baseline
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consumption volume identified via questionnaire.
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at baseline
|
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Self-reported physical activity habits (external personal exposome measure)
Tidsramme: at baseline
|
volume of physical activity practice over a week identified via questionnaire.
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at baseline
|
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Objective-measured physical activity habits (external personal exposome measure)
Tidsramme: at baseline
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volume of physical activity practice over a week identified via actigraphy.
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at baseline
|
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Socioeconomic characteristic (external personal exposome measure)
Tidsramme: at baseline
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level of study identified via questionnaire.
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at baseline
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Socioeconomic characteristic (external personal exposome measure)
Tidsramme: at baseline
|
socio-professional category identified via questionnaire.
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at baseline
|
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Psychological health (external personal exposome measure)
Tidsramme: at baseline
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anxiety assessed using the Hospital Anxiety and Depression Scale (HAD).
The scale comprises 14 items.
The total score ranges from 0 to 21, with a higher score being worse.
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at baseline
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Antatt)
1. september 2030
Primær fullføring (Antatt)
1. september 2031
Studiet fullført (Antatt)
1. september 2031
Datoer for studieregistrering
Først innsendt
11. juni 2026
Først innsendt som oppfylte QC-kriteriene
24. juni 2026
Først lagt ut (Faktiske)
1. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
1. juli 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
24. juni 2026
Sist bekreftet
1. juni 2026
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- 25-PP-25
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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