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Gait, cOgnitiOn & Decline (GOOD)

Gait, cOgnitiOn & Decline (GOOD)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02350270
Enrollment
2800
Registered
2015-01-29
Start date
2015-01-31
Completion date
2015-12-31
Last updated
2015-01-29

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

Conditions

Healthy, Mild Cognitive Impairment, Mild Dementia, Moderate Dementia

Keywords

cognitively healthy individuals

Brief summary

The main objective of the GOOD initiative was to determine which spatio-temporal gait parameters and/or combination(s) of spatio-temporal gait parameters best differentiate between cognitively healthy individuals (CHI), patients with mild cognitive impairment (MCI) and those with mild and moderate dementia.

Detailed description

Gait disorders are frequent in individuals with cognitive disorders. However, the profile of spatio-temporal gait parameters in the different cognitive status in aging (from normal cognition to dementia) has been poorly studied. Determining this profile associated with the severity of cognitive disorders may be helpful to understand the complex interplay between gait and cognitive disorders and, thus, may have important implication for the diagnosis process of patients with and without dementia. For instance, defining a motor phenotype of the severity of cognitive disorders by using quantitative gait measurements could be used to improve the prediction and the diagnosis of dementia. The investigators hypothesized that, compared to CHI, people with MCI and mild dementia could be characterized by specific phenotypes of spatio-temporal gait parameters measured with the GAITRite® system, and that these profiles could be explained by declines in domain-specific cognitive performance.

Interventions

OTHERgait and cognitive testing

Sponsors

Biomathics
CollaboratorUNKNOWN
University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Being 60 years old and older * Ability to answer questions

Exclusion criteria

* Opposition to the use of information collected for research purposes

Design outcomes

Primary

MeasureTime frameDescription
Spatio-temporal gait parametersThis outcome is assessed at inclusionSpatio-temporal gait parameters were measured at steady state walking using GAITRite®-system.

Secondary

MeasureTime frameDescription
Clinical assessmentThis outcome is assessed at inclusionThis outcome was assessed by a questionnaire.
Cognitive statusThis outcome is assessed at inclusionCognitive status was assessed by cognitive testing.

Countries

France

Contacts

Primary ContactOlivier Beauchet, MD, PhD
olbeauchet@chu-angers.fr++33 2 41 35 57 38

Outcome results

None listed

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