Skip to main content
Clinical Trials/ISRCTN97853380
ISRCTN97853380
Completed
未知

Investigating attentional function and cognitive fluctuations in Lewy body disease: a functional magnetic imaging and electrophysiology multicentre non-randomised observational diagnosis cross-sectional study

orthumbria Tyne and Wear NHS Foundation Trust (UK)0 sites96 target enrollmentOctober 21, 2010

Overview

Phase
未知
Intervention
Not specified
Conditions
Topic: Dementias and Neurodegenerative Diseases Research Network
Sponsor
orthumbria Tyne and Wear NHS Foundation Trust (UK)
Enrollment
96
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Registry
who.int
Start Date
October 21, 2010
End Date
April 30, 2013
Last Updated
7 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
orthumbria Tyne and Wear NHS Foundation Trust (UK)

Eligibility Criteria

Inclusion Criteria

  • 1\. For dementia patients: that they meet defined clinical criteria for diagnosis of dementia (dementia with Lewy bodies, Parkinson's disease with dementia, or Alzheimer's dementia) and Mini\-Mental State Examination (MMSE) test score of more than 12
  • 2\. For healthy controls: No history of psychiatric or neurological brain disease and MMSE score more than 26 and has capacity to consent to participate
  • 3\. All aged 60 years and above, either sex

Exclusion Criteria

  • 1\. Contraindications for or unwillingness to undergo MR imaging
  • 2\. Severe dementia (MMSE score less than 12\), as such subjects will have difficulty fully understanding the nature and extent of the proposed research
  • 3\. Presence of other severe or unstable medical illnesses
  • 4\. Subjects with a history of visual impairment secondary to glaucoma, cataract, or macular degeneration as this could affect the ability of subjects to perform the visual attention task with LBD
  • 5\. Medications: subjects on benzodiazepines, antipsychotics or anticonvulsants will not be included as these can effect the EEG activity patterns

Outcomes

Primary Outcomes

Not specified

Similar Trials