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Clinical Trials/NCT01315704
NCT01315704
Unknown
N/A

Maladie d'Alzheimer et Maladies apparentées : Caractérisation Des Anomalies Cognitivo-motrices, et Des Effets Des médicaments Anti-démence et de la Vitamine D à Partir de la Mise en Place d'Une Base de données au CMRR du CHU d'Angers

University Hospital, Angers1 site in 1 country700 target enrollmentNovember 2009

Overview

Phase
N/A
Intervention
Drug intervention
Conditions
Alzheimer's Disease
Sponsor
University Hospital, Angers
Enrollment
700
Locations
1
Primary Endpoint
Spatiotemporal gait parameters
Last Updated
15 years ago

Overview

Brief Summary

The purpose of this study is to compare characteristics of gait and balance measured among patients with Alzheimer's disease or related disorders separated into 3 groups according to the stage of disease (i.e., pre-dementia, mild and moderate dementia stages); to determine the effects of anti-dementia drugs and vitamin D on cognitive motor abnormalities; and to establish a database at Angers University Memory Centre.

Detailed Description

Although gait disorders are frequently associated with Alzheimer's disease and related disorders (ADRD), few studies have focused on cognitive motor effects of anti-dementia drugs and vitamin D. The objectives of this study are to * Compare characteristics of gait and balance measured among patients with ADRD separated into 3 groups according to stages of disease (i.e., pre-dementia, mild and moderate dementia stages) * To determine the effects of anti-dementia drugs and vitamin D on cognitive motor abnormalities * To determine whether motor abnormalities could be associated with cognitive impairments, specifically executive dysfunctions * To establish a database at Angers University Memory Center.

Registry
clinicaltrials.gov
Start Date
November 2009
End Date
November 2017
Last Updated
15 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Angers

Eligibility Criteria

Inclusion Criteria

  • All elderly patients from the University Memory Center of Angers University Hospital.
  • Able to walk without any walking aid on 15 meters
  • Mini-Mental Status Examination score \> 10
  • Being affiliated to a social security regime

Exclusion Criteria

  • Mini-Mental Status Examination score ≤ 10
  • Subject suffering from pre-existing impellent disturbances
  • History of cerebrovascular accident or other cerebro-spinal pathology
  • Poor workmanship of the written or oral French language
  • Use of walking aid such as walking frame with wheels or tricycle.
  • Acute medical or surgical disease in the past 3 months
  • Refusal to participate (or trustworthy person)
  • Near visual acuity \< 2/10

Arms & Interventions

Group 1

Patients with Mild Cognitive Impairment

Intervention: Drug intervention

Group 2

Patients with Mild Alzheimer's disease or related disorders

Intervention: Drug intervention

Group 3

Patients with Moderate Alzheimer's disease or related disorders

Intervention: Drug intervention

Outcomes

Primary Outcomes

Spatiotemporal gait parameters

Time Frame: baseline

Study Sites (1)

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