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Recruiting NCT06716528

NCT06716528 Web-based Application to Test for Long-term Cognitive Deficits in BioCog Patients

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Clinical Trial Summary
NCT ID NCT06716528
Status Recruiting
Phase
Sponsor Charite University, Berlin, Germany
Condition Cognitive Deficits
Study Type OBSERVATIONAL
Enrollment 434 participants
Start Date 2025-01-07
Primary Completion 2026-04

Trial Parameters

Condition Cognitive Deficits
Sponsor Charite University, Berlin, Germany
Study Type OBSERVATIONAL
Phase N/A
Enrollment 434
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-01-07
Completion 2026-04

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Brief Summary

In the present study, a long-term cognitive follow-up of participants of the BioCog cohort (data collection period 2014 - 2019, Ethical vote No: EA2/092/14) from the Berlin study center is to be will be performed in order to record long-term cognitive sequelae (7 to 10 years after study inclusion). In addition to a medical telephone/video visit, the follow-up includes the collection of cognitive tests via web applications and questionnaires of acceptance and usability in the home environment. The study data are analysed in cooperation with the University of Bonn, University Medical Center Schleswig-Holstein and the University of Essen.

Eligibility Criteria

Patients Inclusion Criteria: * Patients of Berliner BioCog cohort with cognitive Testing (CANTAB Research Suite) at Baseline and with plasma samples for baseline that can be contacted. * Written informed consent for participation in the BioCog-Web study. * Data and reserve samples from patients in the Berlin BioCog cohort who can no longer be contacted. Exclusion Criteria: * None Subjects Inclusion Criterion: -BioCog subjects of the non-operated comparison cohort from Berlin with cognitive testing (CANTAB Research Suite) at baseline who are contactable Exclusion criteria: -None

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