- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06268132
Longevity in Russia
Healthy Longevity and Mortality in Long-living Adults: Contributors and Causes - Lifestyle, Socioeconomic Background, and Replicative Aging
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.
Study Overview
Status
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.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Veronika V. Erema, M.D., Ph.D
- Phone Number: 4136 +7 (495) 540-61-71
- Email: VErema@cspfmba.ru
Study Contact Backup
- Name: Daria A. Kashtanova, M.D., Ph.D
- Phone Number: 4120 +74955406171
- Email: DKashtanova@cspfmba.ru
Study Locations
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Moscow, Russian Federation, 129226
- Recruiting
- RUSSIAN CLINICAL AND RESEARCH CENTER OF GERONTOLOGY, Pirogov Russian National Research Medical University of the Ministry of Healthcare of the Russian Federation
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Contact:
- Irina D. Strazhesko, M.D., Ph.D
- Phone Number: +7 (499) 187-64-67
- Email: Istrazhesko@gmail.com
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Long-living individuals
Long-living individuals at least 90 years of age from the Central Federal District of Russia
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mortality among long-living adults
Time Frame: at least 1 year after inclusion in the study
|
Mortality among long-living adults within at least 1 year after inclusion in the study and factors associated with mortality will be assessed.
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at least 1 year after inclusion in the study
|
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Morbidity among long-living adults
Time Frame: at least 1 year after inclusion in the study
|
Morbidity among long-living adults within at least 1 year after inclusion in the study and factors associated with morbidity will be assessed.
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at least 1 year after inclusion in the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Aging phenotypes
Time Frame: at least 2 years after inclusion in the study
|
Identification of successful and unsuccessful aging phenotypes
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at least 2 years after inclusion in the study
|
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Social, economic, and medical- history-related determinants
Time Frame: at least 2 years after inclusion in the study
|
Identification of social, economic, and medical- history-related determinants of successful and unsuccessful aging, geriatric syndromes
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at least 2 years after inclusion in the study
|
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Genetic determinants
Time Frame: at least 2 years after inclusion in the study
|
Identification of the genetic determinants of successful and unsuccessful aging, geriatric syndromes
|
at least 2 years after inclusion in the study
|
|
Epigenetic determinants
Time Frame: at least 2 years after inclusion in the study
|
Identification of the epigenetic determinants (methylation sites) of successful and unsuccessful aging, geriatric syndromes
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at least 2 years after inclusion in the study
|
|
Metagenomic determinants
Time Frame: at least 2 years after inclusion in the study
|
Identification of the metagenomic determinants (16S-rSeq) of successful and unsuccessful aging, geriatric syndromes
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at least 2 years after inclusion in the study
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Irina D. Strazhesko, M.D., Ph.D, Pirogov Russian National Research Medical University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MLS90
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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