Gait and Alzheimer Interaction Tracking (GAIT) Study

Completed

• Conditions: Impaired Cognition; Cerebral Atrophy; Gait Apraxia; Alzheimer Disease

• Registration Number: NCT01315717
• Lead Sponsor: University Hospital, Angers

Brief Summary

The purpose of this study is to examine and to compare gait characteristics under single- and dual-task conditions among healthy subjects together with AD patients at different stages of disease (i.e., pre-dementia, mild and moderate dementia stages).

Detailed Description

Although gait disorders are frequently associated with Alzheimer's disease (AD), few studies have focused on their characterization and mechanism. Exploring the associations of the gait characteristics - more particularly the gait variability - with the cognitive performance of AD patients on one hand, and with the morphological brain abnormalities on the other hand, could be useful to understanding the mechanisms of gait disorders in AD.

The main objective of this study is to examine and to compare gait characteristics under single- and dual-task conditions among healthy subjects together with AD patients at different stages of disease (i.e., pre-dementia, mild and moderate dementia stages).

Study Timeline

• Study Start: 2009-11
• Status Verified: 2011-03
• Study First Submitted: 2011-03-10
• Study First Submitted QC: 2011-03-14
• Study First Posted: 2011-03-15
• Primary Completion: 2016-05
• Study Completion: 2016-05
• Last Update Submitted: 2016-09-21
• Last Update Posted: 2016-09-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 912

Inclusion Criteria

• Age ≥ 60 years
• Able to walk without walking aid on 15 metres
• Score of Mini-Mental Examination (MMSE) > 10
• Written informed consent to participate in the study (or trustworthy person)
• Being affiliated to a social security regime
• Near visual acuity ≥ 2/10
• Absence of severe depression (score in the 15-item Geriatric Depression Scale ≤ 10)

Exclusion Criteria

• Score of Mini-Mental Examination (MMSE) ≤ 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
• Refusal of subject to be informed on possible hanging bare anomaly during study
• Use of walking aid
• Acute medical or surgical disease in the past 3 months
• Refusal to participate (or trustworthy person)
• Contra-indication to the achievement of a Magnetic Resonance Imaging
• Near visual acuity < 2/10
• Presence of severe depression (score in the 15-item Geriatric Depression Scale > 10)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Stride-to-stride variability of stride time	baseline

Trial Locations

Locations (1)

Angers University Hospital; 🇫🇷 Angers, France