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

NCT05155397, Active not recruiting, Technical University of Dortmund

Trial 8

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleThe Dortmund Vital Study: Impact of Biological and Lifestyle Factors on Cognitive Performace and Work AbilityClinicalTrials.gov
NCT numberNCT05155397ClinicalTrials.gov
StatusActive not recruitingClinicalTrials.gov
Enrollment627 participants, actualClinicalTrials.gov
Lead sponsorTechnical University of DortmundClinicalTrials.gov
ConditionsAge-related Cognitive DeclineClinicalTrials.gov
First posted2021-12-13ClinicalTrials.gov
Last updated2026-10-02ClinicalTrials.gov

Registered outcomes 52

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryChange in performance on global cognitive composite score assessed by neuropsychological testsBaseline and 5, 10, 15 years
Change in performance on global cognitive composite score based on measures from neuropsychological tests: Digit-Span forward and backward, semantic memory in written and spoken versions (Word-Fluency), selective attention and attentional endurance (D2-R), crystallized intelligence (Multiple Choice Vocabulary Test), general cognitive status (Mini-Mental-State-Examination; MMSE), different aspects of verbal memory like learning performance and retrieval (Verbal Learning and Memory Tests; VLMT), psychomotor performance and speed of processing (Digit-Symbol-Test), interference control and inhibition (Stroop Test), task switching (Trail-Making-Test; TMT-A and TMT-B), two subtests from the performance testing system measuring logical reasoning and spatial rotation, and fluid intelligence assessed by Raven's Progressive Matrices.
ClinicalTrials.gov
PrimaryChange in attentional performance and perceptual control as assessed by a computerized Bar TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in attentional performance and perceptual control assessed by the Bar Task.ClinicalTrials.gov
PrimaryChange in vigilance control as assessed by a computerized Psychomotor Vigilance TestBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in a Psychomotor Vigilance Test.ClinicalTrials.gov
PrimaryChange in stimulus-response compatibility and conflict processing assessed by the computerized Simon TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the Simon task.ClinicalTrials.gov
PrimaryChange in updating and strategy learning assessed by the computerized AX-CPT TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the AX-CPT task.ClinicalTrials.gov
PrimaryChange in speech understanding and auditory distractibility assessed by computerized Speech-In-Noise perception taskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the Speech-in-noise perception task.ClinicalTrials.gov
PrimaryChange in working memory assessed by the computerized N-back TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the N-back task.ClinicalTrials.gov
PrimaryChange in cue and memory-based task switching assessed by the computerized Task Switching ParadigmBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the cue- and memory based task switching.ClinicalTrials.gov
PrimaryChange in auditive attention and distractibility assessed by the computerized Auditory Distraction TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the Auditory Distraction Task.ClinicalTrials.gov
PrimaryChange in susceptibility to interference and the capacity to inhibit irrelevant stimuli assessed by the computerized Stroop TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the Stroop Task.ClinicalTrials.gov
PrimaryChange in inhibitory control of prepotent responses assessed by the computerized Go/NoGo TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the Go/NoGo Task.ClinicalTrials.gov
PrimaryChange in spatial selective attention assessed by the computerized Visual Search TaskBaseline and 5, 10, 15 yearsChanges in behavioral (speed and accuracy) and electroencephalogram (EEG) data in the Visual Search Task.ClinicalTrials.gov
PrimaryChange in Work Ability IndexBaseline and 5, 10, 15 years
Change in work ability assessed by Work Ability Index (WAI). WAI assess physical and psychological risks to avoid work-related disabilities and early retirement. The index is determined by the employees' answers related to work demands, individual health status and physical and psychological capacities. The total score of WAI is calculated by summing up scores of seven dimensions. The work ability ranged between 7 (insufficient) and 49 points (best work ability).
ClinicalTrials.gov
SecondaryChange in resting state EEG activitybaseline and 5, 10, 15 yearsChange in resting state EEG activity measured for 2 minutes with eyes open, and 2 minutes with eyes closed.ClinicalTrials.gov
SecondaryChange in brain function MRI5, 10, 15 yearsChanges in functional magnetic resonance imaging assessed by resting state MRI.ClinicalTrials.gov
SecondaryChange in brain structure MRI5, 10, 15 yearsChanges in structural resonance imaging assessed by multi-shell diffusion-weighted imaging (DWI).ClinicalTrials.gov
SecondaryChange in Depressive SymptomsBaseline and 5, 10, 15 yearsChange in total score using the Becks Depression Inventory (BDI).ClinicalTrials.gov
SecondaryChange in Burnout SymptomsBaseline and 5, 10, 15 years
Change in total score using the Maslach Burnout Inventory (MBI-D) with 6-point Likert-type scale ranging from 1 (never) to 6 (always), total scores: 14 - 84. Higher scores indicate more severe symptoms.
ClinicalTrials.gov
SecondaryChange in Burnout SymptomsBaseline and 5, 10, 15 years
Change in total score using the Oldenburg Burnout Inventory (OLBI). 4-point Likert-type scale ranging from 1 (strongly agree) to 4 (strongly disagree), total scores: 8 - 32. Higher scores indicate more severe symptoms.
ClinicalTrials.gov
SecondaryChange in Psychosocial Stress SymptomsBaseline and 5, 10, 15 yearsChange in total score using the Psychosocial Stress Questionnaire (PSQ-20).ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 33

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
30534095RESULTPubMed
32923622RESULTPubMed
34216693RESULTPubMed
34676455RESULTPubMed
34682500RESULTPubMed
34859527RESULTPubMed
35285810RESULTPubMed
35675345RESULTPubMed
36358277RESULTPubMed
36525080RESULTPubMed
36682499RESULTPubMed
36881943RESULTPubMed
37099727RESULTPubMed
37204831RESULTPubMed
37397318RESULTPubMed
37410275RESULTPubMed
37450085RESULTPubMed
37685992RESULTPubMed
37861818RESULTPubMed
38398703RESULTPubMed

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 14

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
1-Back TaskPrimary outcomeConductCognition
2-Back TaskPrimary outcomeConductCognition
AX Continuous Performance TestPrimary outcomeConductCognition
Digit Span TestPrimary outcomeConductCognition
Go/No-Go TaskPrimary outcomeConductCognition
Matrix ReasoningPrimary outcomeConductCognition
Psychomotor Vigilance TaskPrimary outcomeConductCognition
Simon TaskPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Symbol CodingPrimary outcomeConductCognition
Task Switching TestPrimary outcomeConductCognition
Trail Making Test APrimary outcomeConductCognition
Trail Making Test BPrimary outcomeConductCognition
Visual Search TestPrimary outcomeConductCognition

Source 4

FieldValueSource
Releasetrials-2026-11-12-0.3.0ClinicalTrials.gov
Release manifest SHA-2564a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.3.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.