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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03399591
Other study ID # 6963
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 2, 2017
Est. completion date March 2019

Study information

Verified date January 2018
Source University Hospital, Strasbourg, France
Contact Jérémie PERISSE, MD
Phone 33 3 88 11 55 11
Email jeremie.perisse@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The prevalence of neurodegenerative diseases will increase over the next decades driven by ageing population. It seems important to develop reliable, replicable and accessible diagnostic tools.

This is a prospective study whose objective is to study the spatio-temporal parameters of gait in patients with Alzheimer's and Lewy body diseases. 64 patients were included in this study. A comparison of the two pathologies was conducted, followed by an analysis based on four groups (mild, severe Alzheimer's disease, mild, severe Lewy body disease) and a study of the severity of the diseases. To study these parameters, we used the Gaitrite treadmill.

The analysis of spatio-temporal parameters of walking in Alzheimer's disease and Lewy body disease enables to identify discriminating variables between the two pathologies. The probability of suffering from an Alzheimer's disease decreases with the pace increase but increases with variations in length of the step, and with the rotation of the foot. While the probability of suffering from Lewy body disease increases with the pace, variations in the step duration, and the duration of double support.

These results are interesting but do not allow to establish a diagnostic score for these two diseases. The monitoring of the variations of these parameters at individual level would probably be more relevant and would enable to detect dual pathologies.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date March 2019
Est. primary completion date March 2019
Accepts healthy volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria:

- Patient over 50

- Hospitalized patient in day hospital

- Patient with an etiological diagnosis of his cognitive disorder

- Patient having a neuropsychological assessment

- Patient able to walk without technical help

- Patient having agreed to participate in the study

Exclusion Criteria:

- Refusal to participate in the study

Study Design


Locations

Country Name City State
France Service de Gériatrie Hôpital de la Robertsau Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary walking test 1 hour after inclusion
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