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Clinical Trial Summary

The purpose of this study is to evaluate the feasibility of administering a 20-day preoperative cognitive training intervention (Cog-Train) to a widely inclusive sample of cardiac surgical patients.


Clinical Trial Description

Cognitive outcomes remain poor after cardiac surgery. Data from the field of cognitive neuroscience suggests that cognitive training, which harnesses the brain's adaptive plasticity to improve, maintain, or restore function in a target area, can be used to strengthen brain resilience and improve cognitive outcomes following challenge. While its effectiveness has been demonstrated in older adults as well as in other (nonsurgical) patient populations, no training intervention like this has ever before been used in any surgical patient in the preoperative period. The purpose of this study is to evaluate the feasibility of administering a 20-day cognitive training intervention (Cog-Train) to a widely inclusive sample of cardiac surgical patients before their surgery. Data obtained will be used to design a full-scale randomised controlled trial (RCT) on Cog-Train's effectiveness in improving postoperative cognitive outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02053207
Study type Interventional
Source Papworth Hospital NHS Foundation Trust
Contact Kimberly Giraud, PhD
Phone 01480 830541
Email kimberly.giraud@papworth.nhs.uk
Status Not yet recruiting
Phase N/A
Start date January 2018
Completion date December 2018

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