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

NCT06716528 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 434

Last updated 2025-11-21

No results posted yet for this study

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.

Conditions

Sponsors & Collaborators

  • University Hospital, Bonn

    collaborator OTHER

  • University Hospital Schleswig-Holstein

    collaborator OTHER

  • Universitätsklinikum Essen

    collaborator OTHER

  • Charite University, Berlin, Germany

    lead OTHER

Principal Investigators

  • Claudia Spies, MD, Prof. · Charitè - University Berlin

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-01-07
Primary Completion
2026-04-30
Completion
2026-04-30

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06716528 on ClinicalTrials.gov