Skip to content

Executive Reaction Time Test in Assessment of Cognitive Dysfunction After Aortic Valve Procedures

Executive Reaction Time Test in Assessment of Cognitive Dysfunction After Aortic Valve Procedures

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01953068
Enrollment
18
Registered
2013-09-30
Start date
2014-01-31
Completion date
2016-05-31
Last updated
2021-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurobehavioral Manifestations

Keywords

POCD, Executive Reaction Time Test, Aortic valve surgery, Cognitive functions, Transcatheter Aortic Valve Implantation

Brief summary

Up to 50% of patients undergoing surgical aortic valve operation suffer from some level of post-operative cognitive dysfunction (POCD). Frontal lobes of the brain, where executive functions are located, are highly susceptible to trauma caused by possible blood malperfusion to these areas of the brain during surgery. Conventional and established neuropsychological test methods are poor in distinguishing these kinds of trauma, as they are isolated, structured tests that do not require multitasking and processing of multiple stimuli at the same time. The phase 1 goal of this study is to employ an experimental Executive reaction time (RT) test to see if this method could improve objective detection of subtle brain dysfunction assumed to underlie persistent cognitive, somatic, and affective complaints reported by patients who have undergone electic aortic valve replacement (AVR) surgery. Phase 2 of the study will concentrate on patients undergoing transcatheter aortic valve implantation (TAVI).

Interventions

None listed

Sponsors

Tampere University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* undergoing elective aortic valve stenosis surgery (phase 1) or transcatheter aortic valve implantation (phase 2)

Exclusion criteria

* Previous neurological or psychiatric disorder. * Significant visual problem * Problems with upper arm/hand use

Design outcomes

Primary

MeasureTime frame
Executive Reaction Time Test response speed6 months

Secondary

MeasureTime frame
Executive Reaction Time Test: error% of answers6 months

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026