MoCA vs. MMS: Which Tool to Detect Cognitive Disorders in Oncogeriatric?

NCT ID: NCT03299855

Last Updated: 2023-10-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

104 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-13

Study Completion Date

2023-10-13

Brief Summary

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This study concerns elderly patients with cancer with onco-geriatric assessment.

This study propose to associate the collection of the results with the Mini-Cog and the CODEX with the passing of the MoCA and the MMS tests, as well as a neuropsychological assessment, in order to determine if the patients have cognitive impairments, to evaluate the sensitivity of these 4 screening tests in elderly patients seeking treatment for their cancer. The results of this study will make it possible, where appropriate, to adapt the practice in the context of oncogeriatric assessment.

Detailed Description

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Conditions

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Neoplasms

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Passation of MMS and MoCA tests associated to passation of neuropsychological test
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Interventions

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Passation of neuropsychological test

Passation of MoCA and MMS tests associated with neuropsychological test

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient aged over 70 years
* Patient with cancer (solid tumor or haemopathy) for whom a first line treatment is envisaged (whatever it is). Surgery and radiotherapy are allowed before entry into the study.
* Patient candidate for oncogeriatric assessment
* Patient agree to participate in the study
* Using the French language

Exclusion Criteria

* Primary central nervous system or cerebral metastasis
* Evolutionary psychiatric pathology known (e.g. schizophrenia)
* Severe Visual and / or Auditory Impairment
* Patients unable to respond to cognitive tests
* Patient (s) deprived of liberty, under guardianship or curatorship
* Refusal of participation
Minimum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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UCOG (Unite de coordination en Onco-Gériatrie)

UNKNOWN

Sponsor Role collaborator

Centre Francois Baclesse

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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florence JOLY, prof

Role: PRINCIPAL_INVESTIGATOR

Centre François Baclesse

Locations

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Centre François Baclesse

Caen, , France

Site Status

CHU

Caen, , France

Site Status

CH

Cherbourg, , France

Site Status

Ch Compiegne

Compiègne, , France

Site Status

Centre Henri Becquerel

Rouen, , France

Site Status

Centre Hospitalier

Saint-Lô, , France

Site Status

Countries

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France

Other Identifiers

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2017-A01079-44

Identifier Type: -

Identifier Source: org_study_id

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