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Eye-Tracking Control to Assess Cognitive Functions in Patients with Amyotrophic Lateral Sclerosis
Published on: October 13, 2016
Cognitive function in patients with late stage amyotrophic lateral sclerosis
J Lakerveld1, B Kotchoubey, A Kübler
1Institute of Medical Psychology and Behavioural Neurobiology, University of Tübingen, Tübingen, Germany. j.lakerveld@vumc.nl
Late-stage amyotrophic lateral sclerosis (ALS) patients showed normal cognitive function, with learning and memory performance correlating with disease progression. This challenges previous assumptions about cognitive decline in ALS.
Area of Science:
- Neuroscience
- Neurology
Background:
- Amyotrophic lateral sclerosis (ALS) is associated with cognitive deficits, particularly in early stages.
- Cognitive function in late-stage ALS remains understudied due to limitations of standard neuropsychological tests.
- Motor and speech impairments in advanced ALS preclude traditional cognitive assessments.
Purpose of the Study:
- To investigate cognitive function in late-stage amyotrophic lateral sclerosis (ALS) patients.
- To assess cognitive performance in relation to disease-specific functional status.
- To adapt neuropsychological testing for severely physically impaired individuals.
Main Methods:
- A neuropsychological test battery was administered to 11 late-stage ALS patients and matched controls.
- Testing focused on tasks with binary (yes/no) responses, avoiding verbalization and reaction time measures.
- Cognitive function was explored in relation to disease-related functional status.
Main Results:
- Overall cognitive function in late-stage ALS patients was found to be normal.
- Some patients exhibited deficits in executive function, learning, and memory.
- A significant negative correlation was observed between performance on learning/memory tasks and patient functional status.
Conclusions:
- Late-stage ALS patients with more advanced disease showed superior performance in learning and memory tasks.
- Cognitive function in ALS may not uniformly decline and can be preserved or even enhanced in certain domains.
- Findings suggest a complex relationship between cognitive function and disease progression in amyotrophic lateral sclerosis.
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