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Clinical Trials in Germany / NCT05155397
Active, not recruiting Observational

The Dortmund Vital Study: Impact of Biological and Lifestyle Factors on Cognitive Performace and Work Ability

NCT05155397 · tracked via the Priya Life Science Germany tracker
Sponsor
Technical University of Dortmund
Phase
Observational
Started
2016-04
Last updated
2024-12-03

Condition(s) studied

Age-related Cognitive Decline

Study summary

The goal of the Dortmund Vital Study is to validate previous hypotheses and to generate and validate new hypotheses about the relationship of ageing, working conditions, genetic makeup, stress, metabolic functions, cardiovascular system, immune system, and mental performance over the lifespan with a focus on healthy working adults. The Dortmund Vital Study is a multidisciplinary longitudinal study involving the Departments of Ergonomics, Immunology, Psychology and Neurosciences, and Toxicology of the Leibniz Research Centre for Working Environment and Human Factors at the TU Dortmund (IfADo) in Dortmund, Germany, as well as several national and international cooperation partners.

Eligibility

Sex
ALL
Min age
20 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Blood thinners * Hormones * Antihypertensives * Cholesterol reducers * Normal or corrected-to-normal vision and hearing * Fulfill standard inclusion criteria for MRI measurements * Sufficient language skills Exclusion Criteria: * Dementia * Parkinsonism * Stroke * Cardiovascular diseases * Bleeding tendency * Oncological diseases * Schizophrenia * Obsessive-compulsive disorder * Anxiety disorders * Severe depression * Head injuries * Head surgery * Head implants * Eye diseases (cataract, glaucoma, blindness) * Accidents that limit physical fitness and mobility * Psychotropic drugs * Neuroleptics

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Technical University of Dortmund, Leibniz Research Centre for Working Environment and Human Factors Dortmund Germany
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05155397 on ClinicalTrials.gov ↗ ← All trials in Germany