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Longevity in Russia

Healthy Longevity and Mortality in Long-living Adults: Contributors and Causes - Lifestyle, Socioeconomic Background, and Replicative Aging

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06268132
Enrollment
4000
Registered
2024-02-20
Start date
2019-12-25
Completion date
2025-12-31
Last updated
2024-02-22

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

Conditions

Age-related Cognitive Decline, Aging, Aging Disorder, Frailty, LONGEVITY 1

Brief summary

This is an observational cohort study of long-living adults (participants aged 90 and above) from the Central Federal District of Russia. The study seeks to determine the genetic and cellular and molecular determinants of healthy longevity and to assess the impact of lifestyle and socioeconomic and environmental factors on healthy longevity. The study is expected to result in the development of a panel of markers of healthy longevity and/or a model of healthy aging based on the analysis of all factors under consideration.

Detailed description

The study involves a long-term observation of a cohort of long-living adults. During the first visit, a medical professional will take a detailed medical history and perform a comprehensive geriatric assessment (for 15 geriatric syndromes), and physical examination. The participants will have their biomaterials sampled for basic and extended blood biochemistry testing, telomere length measurement, common urine tests and subsequent biobanking and additional studies: whole genome sequencing, DNA methylation analysis, transcriptome analysis, and 16S RNA sequencing of stool and saliva. Follow-up checks will be carried out once a year by phone or during additional visits. The study seeks to identify the genetic, epigenetic, and metagenomic determinants associated with the successful and unsuccessful aging phenotypes, mortality, and survival in long-living individuals.

Interventions

None listed

Sponsors

Pirogov Russian National Research Medical University
CollaboratorOTHER
Center for Strategic Planning, of the Federal Medical and Biological Agency
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
90 Years to No maximum

Inclusion criteria

* Informed consent * 90 years of age or above

Exclusion criteria

* Refusal to participate or to provide informed consent; * Any other criteria deemed reasons for exclusion by the Principal Investigator.

Design outcomes

Primary

MeasureTime frameDescription
Mortality among long-living adultsat least 1 year after inclusion in the studyMortality among long-living adults within at least 1 year after inclusion in the study and factors associated with mortality will be assessed.
Morbidity among long-living adultsat least 1 year after inclusion in the studyMorbidity among long-living adults within at least 1 year after inclusion in the study and factors associated with morbidity will be assessed.

Secondary

MeasureTime frameDescription
Genetic determinantsat least 2 years after inclusion in the studyIdentification of the genetic determinants of successful and unsuccessful aging, geriatric syndromes
Aging phenotypesat least 2 years after inclusion in the studyIdentification of successful and unsuccessful aging phenotypes
Metagenomic determinantsat least 2 years after inclusion in the studyIdentification of the metagenomic determinants (16S-rSeq) of successful and unsuccessful aging, geriatric syndromes
Epigenetic determinantsat least 2 years after inclusion in the studyIdentification of the epigenetic determinants (methylation sites) of successful and unsuccessful aging, geriatric syndromes
Social, economic, and medical- history-related determinantsat least 2 years after inclusion in the studyIdentification of social, economic, and medical- history-related determinants of successful and unsuccessful aging, geriatric syndromes

Countries

Russia

Contacts

Primary ContactDaria A. Kashtanova, M.D., Ph.D
DKashtanova@cspfmba.ru+74955406171
Backup ContactVeronika V. Erema, M.D., Ph.D
VErema@cspfmba.ru+7 (495) 540-61-71

Outcome results

None listed

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