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.

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
4,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2019

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 25, 2019

Completed
4.1 years until next milestone

First Submitted

Initial submission to the registry

February 13, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 20, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

February 22, 2024

Status Verified

February 1, 2024

Enrollment Period

5 years

First QC Date

February 13, 2024

Last Update Submit

February 20, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • Mortality among long-living adults

    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

    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 Outcomes (5)

  • Aging phenotypes

    at least 2 years after inclusion in the study

  • Social, economic, and medical- history-related determinants

    at least 2 years after inclusion in the study

  • Genetic determinants

    at least 2 years after inclusion in the study

  • Epigenetic determinants

    at least 2 years after inclusion in the study

  • Metagenomic determinants

    at least 2 years after inclusion in the study

Study Arms (1)

Long-living individuals

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

Eligibility Criteria

Age90 Years+
Sexall
Age GroupsOlder Adult (65+)
Sampling MethodNon-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

You may qualify if:

  • Informed consent
  • years of age or above

You may not qualify if:

  • Refusal to participate or to provide informed consent;

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

RUSSIAN CLINICAL AND RESEARCH CENTER OF GERONTOLOGY, Pirogov Russian National Research Medical University of the Ministry of Healthcare of the Russian Federation

Moscow, 129226, Russia

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Whole blood, serum, stool, saliva, urine

MeSH Terms

Conditions

Frailty

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Irina D. Strazhesko, M.D., Ph.D

    Pirogov Russian National Research Medical University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Daria A. Kashtanova, M.D., Ph.D

CONTACT

Veronika V. Erema, M.D., Ph.D

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 13, 2024

First Posted

February 20, 2024

Study Start

December 25, 2019

Primary Completion

December 31, 2024

Study Completion

December 31, 2025

Last Updated

February 22, 2024

Record last verified: 2024-02

Locations