ClinicalTrials.gg
Status unknownNCT03399591Updated Jul 6, 2018

Gait Disorders in Patients With Cognitive Decline

An observational study in Gait Disorders, Neurologic, sponsored by University Hospital, Strasbourg, France. Status unknown at 1 site in France. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2018-07-06.

Sponsored by University Hospital, Strasbourg, France · Observational

The sponsor has not verified this record recently (last verified Jan 2018), so the status shown — last known as Recruiting — may be out of date.

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Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
50 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 22 studies in Gait Disorders, Neurologic with a site in France — 4 open to participants now, 4 under way, none of them phase 3. Gait Disorders, Neurologic · France.

Started
2017
with 1 other
Observational
8 of 22
2 open now
Registered
7th of 22
by date

Among the 22 studies in Gait Disorders, Neurologic with a site in France, this one is one of 2 that started in 2017, is one of 8 observational ones, and was the 7th registered.

Gait Disorders, Neurologic

346 studies on the registry are indexed under Gait Disorders, Neurologic; 54 are open to participants now.

Browse Gait Disorders, Neurologic studies →

Open to participants now

4 of the 22 studies in Gait Disorders, Neurologic with a site in France are open now. Recruiting first, the newest first:

All 4 open studies →

A study can be open while its sites in France have not opened yet or have stopped. Only those recruiting at a site in France →

Who these studies take

Of the 36 Gait Disorders, Neurologic studies recruiting now, 14 (39%) set no upper age limit and 19 (53%) stop at 75 or younger; 5 take children under 18; 5 take healthy volunteers.

This study: 50 Years and older · all sexes.

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02

Study 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.

03

Conditions studied

  • Gait Disorders, Neurologic

Keywords

  • Gait Disorders
  • Spatio-temporal parameters of walking
  • Alzheimer's disease
  • Lewy body disease
04

Who can participate

Ages eligible
50 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Patient over the age of 50 with a gait disorder

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

Exclusion Criteria:

  • Refusal to participate in the study
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. walking test

    Time frame: 1 hour after inclusion

07

Study locations

1 of 1 sites recruiting
  • Service de Gériatrie Hôpital de la Robertsau
    Strasbourg, 67000, France
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started May 2017 (actual). Primary completion is estimated for Mar 2019, 22 months after the start.

Of 45 non-industry observational studies under Gait Disorders, Neurologic, half reached primary completion within 18 months of starting (the median), counting those still running; a quarter within 3 and three quarters within 46. This study's planned 22 months is above that.

Counting every sponsor, half of 46 studies reached it within 17 months; a quarter within 3 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 8, 2018
First posted
Jan 16, 2018
StartActual
May 2, 2017
Primary completionEst.
Mar 2019
CompletionEst.
Mar 2019
Last update
Jul 6, 2018
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 6, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03399591
Responsible party
Sponsor
First posted
Jan 16, 2018
Start date
May 2, 2017
Primary completion
Mar 2019 (estimated)
Completion
Mar 2019 (estimated)
Last update
Jul 6, 2018

Study contacts

Jérémie PERISSE, MD
Contact
jeremie.perisse@chru-strasbourg.fr
33 3 88 11 55 11
Candice Muller, MD
Contact
candice.muller@chru-strasbourg.fr
33 3 88 11 55 11
Jérémie PERISSE, MD
principal investigator · University Hospital, Strasbourg, France

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2018. You cannot join it, but the record below documents what was studied.

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Discussion

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