Web-based Application to Test for Long-term Cognitive Deficits in BioCog Patients
Charite University, Berlin, Germany
434 participants
Jan 7, 2025
OBSERVATIONAL
Conditions
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
Inclusion Criteria4
- Patients
- 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 Criteria5
- 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
- None
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Locations(1)
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NCT06716528