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A Registered Cohort Study on Color Discrimination Deficit Associated With Neurodegenerative Disorders.

A Registered Observational Cohort Study on Color Discrimination Deficit Associated With Neurodegenerative Disorders.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05639140
Enrollment
500
Registered
2022-12-06
Start date
2018-01-01
Completion date
2025-07-01
Last updated
2022-12-06

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

Conditions

Neurodegenerative Disorders

Brief summary

Color discrimination deficit is a common manifestation of Alzheimer's disease (AD). However, the pathophysiology of this dysfunction remains poorly understood. The aim of the present study was to evaluate color discrimination using the Farnsworth-Munsell 100 hue test in patients with AD and mild cognitive impairment (MCI), compared with age-matched control subjects. As a secondary aim, we evaluated whether the outcomes of these visual tests were associated with cognitive.

Interventions

OTHERData collection

Neuropsychological assessment, FM-1OO, brain MRI, electroencephalogram and biomarker datas will be collected

Sponsors

Fujian Medical University Union Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* All patients underwent extensive clinical examination including thorough neurological and somatic examination by a specialized neurologist or geriatrician and extensive neuropsychological examination by a trained psychologist. AD was diagnosed according to the NINCDS-ADRDA criteria.

Exclusion criteria

* We excluded individuals with noncompensated somatic illnesses, a history of a psychiatric disorder, color blindness, ophthalmological pathology, severe cranial trauma, focal neurological signs or magnetic resonance imaging examinations suggestive of cerebrovascular disturbances.

Design outcomes

Primary

MeasureTime frameDescription
MoCA scoresBaselineThe Montreal Cognitive Assessment (MoCA)

Secondary

MeasureTime frameDescription
ACE-III scoresBaselineAddenbrooke's Cognitive Examination (ACE) score

Other

MeasureTime frameDescription
TESBaselineThe total error score

Countries

China

Contacts

Primary ContactXiaodong Pan, Doctor
pxd77316@163.com0591-86218341

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026