MedPath

Cognitive Training to Improve Cognitive Function Following Chemotherapy

Not Applicable
Conditions
Cognitive Dysfunction
Registration Number
NCT01013233
Lead Sponsor
Charite University, Berlin, Germany
Brief Summary

The purpose of this study is to improve cognitive dysfunction following chemotherapy, the investigators investigated to see whether a cognitive training for memory and concentration skills can improve cognitive performance in patients following cancer treatment.

Detailed Description

Patients following chemotherapy invited for a cognitive training. Before and after cognitive function will evaluate.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • patients with cancer 6 weeks after chemotherapy
Exclusion Criteria
  • patients with neurological or psychiatric disorders
  • patients without compliance

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
several cognitive tests (TAP, VLMT, TMT, Stroop, RWT, D2, LGT-3)one weeks following the end of the cognitive training
Secondary Outcome Measures
NameTimeMethod
quality of life and subjective perception of cognitive problems7 weeks

Trial Locations

Locations (1)

Charite Universitätsmedizin Berlin

🇩🇪

Berlin, Germany

Charite Universitätsmedizin Berlin
🇩🇪Berlin, Germany
Susanne Effenberger, MSc
Contact
+49-30-8445-2410
susanne.effenberger@charite.de
susanne Effenberger, MSc
Principal Investigator

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.