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

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

Observational

Enrollment (Estimated)

4000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

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

Study Locations

      • 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
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

The inclusion of participants will be carried out with the involvement of social services, boarding houses for labor veterans, geriatric centers and other geriatric services in the central region of Russia

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Long-living individuals
Long-living individuals at least 90 years of age from the Central Federal District of Russia

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.
at least 1 year after inclusion in the study
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.
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
at least 2 years after inclusion in the study
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
at least 2 years after inclusion in the study
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
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
at least 2 years after inclusion in the study

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Irina D. Strazhesko, M.D., Ph.D, Pirogov Russian National Research Medical University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 25, 2019

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

December 31, 2025

Study Registration Dates

First Submitted

February 13, 2024

First Submitted That Met QC Criteria

February 13, 2024

First Posted (Actual)

February 20, 2024

Study Record Updates

Last Update Posted (Estimated)

February 22, 2024

Last Update Submitted That Met QC Criteria

February 20, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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