NCT06953180

Brief Summary

This study aims to enhance personalized and preventive care for non-communicable diseases (NCDs) in Kazakhstan by examining epigenetic factors, predicting biological age and reproductive function using machine learning, and developing health improvement recommendations.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
6,720

participants targeted

Target at P75+ for all trials

Timeline
8mo left

Started Mar 2025

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress64%
Mar 2025Dec 2026

Study Start

First participant enrolled

March 3, 2025

Completed
28 days until next milestone

First Submitted

Initial submission to the registry

March 31, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 1, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2026

Completed
12 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Expected
Last Updated

July 11, 2025

Status Verified

April 1, 2025

Enrollment Period

10 months

First QC Date

March 31, 2025

Last Update Submit

July 8, 2025

Conditions

Keywords

DNA methylationprecision medicinepreventive medicineartificial intelligencebiomedical modeling

Outcome Measures

Primary Outcomes (2)

  • Accuracy of Machine Learning Model for Predicting Biological Age

    Evaluation of the model's performance (based on telomere length and DNA methylation) using Mean Absolute Error (MAE), Mean Squared Error (MSE), and R².

    Within 10 months from start of data collection

  • Accuracy of Reproductive Function Prediction Model

    Development and validation of machine learning model to predict reproductive function using biomarkers. Model performance evaluated via MAE, MSE, and R².

    Within 10 months from start of data collection

Study Arms (1)

The study includes 1 cohort divided into 4 age subgroups.

The study follows a multistage cluster sampling design with age and gender stratification. A total of 1 cohorts have been identified, further divided into 4 age subgroups: 1. 18-29 years 2. 30-44 years 3. 45-59 years 4. 60-69 years Each age group is designed to have an equal distribution of men and women, ensuring gender balance across all subgroups.

Other: Genetic: DNA analysis

Interventions

Investigation of telomere length (TL) and DNA methylation level analysis

The study includes 1 cohort divided into 4 age subgroups.

Eligibility Criteria

Age18 Years - 69 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The study population consists of 6,720 adult volunteers aged 18 to 69 years, residing across 17 regions of Kazakhstan. Participants are stratified by age and gender to ensure balanced representation within the following age groups: * 18-29 years * 30-44 years * 45-59 years * 60-69 years Each age group includes an equal proportion of men and women, ensuring gender balance. The selection follows a multistage cluster sampling design, incorporating various socioeconomic backgrounds and health statuses to enhance the generalizability of findings.

You may qualify if:

  • Adults aged 18 to 69 years.
  • Residents of 17 regions of Kazakhstan.
  • Willingness to participate and provide informed consent.

You may not qualify if:

  • Age less than 18 years old or over 69 years old.
  • Failure to provide informed consent or incomplete participation in data collection procedures.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Asfendiyarov Kazakh National Medical University

Almaty, Kazakhstan, 050000, Kazakhstan

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Venous blood samples and peripheral blood mononuclear cells (PBMCs) will be collected. DNA will be extracted and analyzed for telomere length (via quantitative real-time polymerase chain reaction (qPCR)) and methylation patterns (using methylation-sensitive high-resolution melting (MS-HRM)). Only high-quality DNA (assessed by spectrophotometry and fluorometry) will be retained. Samples will be stored at -80°C.

MeSH Terms

Conditions

Cardiovascular DiseasesDiabetes Mellitus, Type 2ObesityRenal Insufficiency, Chronic

Condition Hierarchy (Ancestors)

Diabetes MellitusGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesOverweightOvernutritionNutrition DisordersBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsRenal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic Processes

Central Study Contacts

Ildar Fakhradiyev, Ph.D

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Vice-rector

Study Record Dates

First Submitted

March 31, 2025

First Posted

May 1, 2025

Study Start

March 3, 2025

Primary Completion

January 1, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

July 11, 2025

Record last verified: 2025-04

Locations