Telecommunication Technology-based Online Survey
New Challenges for the Population on the Path to Achieving Active Longevity: an Online Survey of Respondents Using Telecommunication Technologies
1 other identifier
observational
2,000
1 country
1
Brief Summary
The aim of this study is to identify and assess new health-associated risk factors, including clinical-pharmacological risk factors. The cohort is built using telecommunication approaches. The associations between clinical-pharmacological, social, demographic, behavioral, and environmental characteristics will be assessed. The continuous depersonalized online survey is performed using the original informational resources in the form of specially designed web-site aimed at identification and assessment of population-based pharmacotherapy patterns including characteristics of self-medication, biologically active food supplement intake, polypharmacy, and adverse drug-drug interactions in the people residing in the ecological conditions of various regions of the country. The invitations to participate in the online survey are sent via the SMS messages using the SMS-Target tool provided by OOO T2 Mobile Company. The survey is performed online at www.zdorov.tpu.ru and www.zdorov.expert both specifically designed for questionnaire publication and data accumulation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2022
Longer than P75 for all trials
1 active site
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 2, 2022
CompletedFirst Submitted
Initial submission to the registry
November 28, 2023
CompletedFirst Posted
Study publicly available on registry
December 7, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2028
January 27, 2026
January 1, 2026
5.8 years
November 28, 2023
January 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Incidence of serious drug-drug interactions (percent)
Incidence of serious drug-drug interactions (DDIs) is assessed as a percentage (%) of completed survey questionnaires associated with serious DDIs relative to the size of respondent population.
Five years
Median number of serious drug-drug interactions (n)
Median number of serious drug-drug interactions is assessed per one completed survey questionnaire containing information on pharmacotherapy.
Five years
Secondary Outcomes (12)
Incidence of polypharmacy (percent)
Five years
Incidence of MRI administration (percent)
Two years
Incidence of CT administration (percent)
Two years
Incidence of diagnostic ultrasound administration (percent)
Two years
Incidence of diagnostic X-ray administration (percent)
Two years
- +7 more secondary outcomes
Study Arms (1)
Non-structured population
The respondent will represent the non-structured population of the Russian Federation invited to participate in the study using the SMS-Target tool provided by OOO T2 Mobile Company.
Interventions
The participants of the study undergo the online survey at www.zdorov.tpu.ru and www.zdorov.expert.
Genetic testing will be performed in subgroup of survey respondents willing to participate in the study of polymorphisms of genes involved in drug metabolism or affecting biological effects of medications including CYP2D6, ACE, UGT1A1, CYP2C9, and CYP2C19.
Eligibility Criteria
Nonstructured population aged 18 years and older willing to complete the entire questionnaire and signing the informed concent form.
You may qualify if:
- age of 18 years and older
- signing the informed concent form online
- completion of the entire questionnaire
You may not qualify if:
- age under 18 years
- refuse to sign the informed concent form
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tomsk National Research Medical Center, Russian Academy of Sciences
Tomsk, 634012, Russia
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nina D Anfinogenova, PhD
Tomsk NRMC
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- ECOLOGIC OR COMMUNITY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 28, 2023
First Posted
December 7, 2023
Study Start
December 2, 2022
Primary Completion (Estimated)
September 1, 2028
Study Completion (Estimated)
December 31, 2028
Last Updated
January 27, 2026
Record last verified: 2026-01