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Status unknownNCT01993628Updated Nov 25, 2013

Construction-LBD (Constructional Apraxia in Alzheimer's Disease (AD) and Lewy Body's Dementia (LBD))

An interventional study of Rey figure test and MRI in Alzheimer's Disease and Lewy Body's Dementia, sponsored by University Hospital, Strasbourg, France. Status unknown at 1 site in France. Open to participants aged 45 Years and older. Per ClinicalTrials.gov, last updated 2013-11-25.

Sponsored by University Hospital, Strasbourg, France · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Nov 2013), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Non-randomized
Ages
45 Years and older
Sex
All
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Study summary

Alzheimer's disease (AD) and Lewy body's dementia (LBD) are two frequent neurodegenerative pathologies. They differ in their expression, their evolution but share same features which make their diagnosis uneasy.

Constructional apraxia has been described in both disease.The underlying mechanisms have been less studied and could be different in AD and LBD.

The definition of the constructional apraxia is purely descriptive and few models are inconclusive.

It is admitted that drawing tasks involve visuo-perceptive and visuo-spatial abilities, executive functions and working memory as well as purely "constructive" skills.

Regarding to different studies, visuo-perceptive abilities are more severely impaired in LBD than in AD and are considered as an early onset sign of the disease.

Executive functions deficits are documented in AD and LDB and could contribute to the drawing impairment.

It is possible to compensate the planning disorders in giving patient the best strategy to use.

If drawing impairment persists, they should result of others mechanisms like visuo-perception, visuo-spatial or constructive deficits.

The investigators suggest that giving the best planning strategy will help more AD patients who are supposed to fail in raison of an executive impairment, than the LDB group who is supposed to present visuo-perceptive deficits. An MRI will be proposed to study the cerebral areas involved in constructional apraxia.

02

Conditions studied

  • Alzheimer's Disease
  • Lewy Body's Dementia

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03

In context

Alzheimer Disease

3,765 studies on the registry are indexed under Alzheimer Disease; 881 are open to participants now.

This study's planned enrollment of 80 is above the median of 68 across 2,861 interventional studies indexed under Alzheimer Disease.

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Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 989 studies on the registry; 348 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
45 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

  • Alzheimer's disease or Lewy bodies dementia
  • ≥ 45 years
  • the cognitive impairment is mild to moderate
  • French speaker
  • a caregiver is present
  • An informed consent is signed by the patient and the p.i.

Exclusion criteria

Exclusion Criteria:

  • MRI contraindication
  • Other neurological disease (FTD, brain tumor, vascular disease…)
  • Psychiatric disease (Schizophrenia, major depression, psychotic disorders, melancholia…)
  • Patient who doesn't want to be informed in case of the discovery of an abnormality
  • View or audition deficits, or motor disability which can interfere with the cognitive testing
  • Patient participating to an exclusive protocol or in the period of exclusion
  • Pregnant woman
  • Person under an administrative or legal measure of liberty privation
  • Person under a legal measure of protection or under administrative supervision
  • Person unable to give his consent
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Alzheimer's disease (AD)

    Rey figure test and MRI

    Other: Rey figure test · Other: MRI

  • Experimental
    Lewy body's dementia (LBD)

    Rey figure test and MRI

    Other: Rey figure test · Other: MRI

Interventions

  • OtherRey figure test
  • OtherMRI
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What researchers measure

Primary outcomes

  1. Score obtained at the Rey figure test with a planning strategy help by LBD patients compared to the score obtained by AD patients.

    Time frame: At inclusion

07

Study locations

1 of 1 sites recruiting
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Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Oct 2013, a primary completion of Nov 2016 and a completion of Nov 2016. It does not say whether these dates are actual or estimated.

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

Registered
Oct 31, 2013
First posted
Nov 25, 2013
Start
Oct 2013
Primary completionEst.
Nov 2016
CompletionEst.
Nov 2016
Last update
Nov 25, 2013
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 Nov 25, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01993628
Responsible party
Sponsor
First posted
Nov 25, 2013
Start date
Oct 2013
Primary completion
Nov 2016 (estimated)
Completion
Nov 2016 (estimated)
Last update
Nov 25, 2013

Study contacts

Xavier DE PETIGNY, Docteur
Contact
xavier.depetigny@chru-strasbourg.fr
3 88 11 56 24 ext. 0033
PHILLIPPS Clelie, Ingenior
Contact
clelie.phillipps@chru-strasbourg.fr
3 88 12 79 25 ext. 0033
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Nov 2013. You cannot join it, but the record below documents what was studied.

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