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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01013233
Other study ID # KTST09
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 12, 2009
Last updated November 12, 2009
Start date December 2009
Est. completion date October 2011

Study information

Verified date November 2009
Source Charite University, Berlin, Germany
Contact Susanne Effenberger, MSc
Phone +49-30-8445-2410
Email susanne.effenberger@charite.de
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial 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.


Description:

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


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients with cancer 6 weeks after chemotherapy

Exclusion Criteria:

- patients with neurological or psychiatric disorders

- patients without compliance

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
cognitive training
cognitive training over 6 weeks, consist of 6 meetings (a 45minutes), three sessions focus on concentration tasks and three sessions on memory problems.
Other:
control group
no intervention

Locations

Country Name City State
Germany Charite Universitätsmedizin Berlin Berlin

Sponsors (2)

Lead Sponsor Collaborator
Charite University, Berlin, Germany Freie Universität Berlin

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary several cognitive tests (TAP, VLMT, TMT, Stroop, RWT, D2, LGT-3) one weeks following the end of the cognitive training No
Secondary quality of life and subjective perception of cognitive problems 7 weeks No
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