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Validation of Brief Computerized Cognitive Assessment in Multiple Sclerosis (BCCAMS)

Validation of Brief Computerized Cognitive Assessment in Multiple Sclerosis (BCCAMS) - BICAFMS Study (Brief Cognitive Assessment in French MS Patients)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02391064
Acronym
BICAFMS
Enrollment
421
Registered
2015-03-18
Start date
2015-02-17
Completion date
2018-02-18
Last updated
2026-05-14

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

Conditions

Multiple Sclerosis

Keywords

cognition, brief computerized cognitive assessment, impairment prediction

Brief summary

Cognitive disorders are common in early stage of Multiple Sclerosis (MS) and concern mainly information processing speed (IPS) which also influences with other cognitive functions such as attention, working memory and executive functions. The investigators validated a computerized test of IPS, the computerized speed cognitive test (CSCT), which can detect disorders of IPS in MS. A short battery was proposed, the brief cognitive assessment for multiple sclerosis (BICAMS) battery, which combines the Symbol-Digit Modalities-test (SDMT), a test of the IPS, and two measures of episodic memory. On the same principle, the investigators propose to validate a short computerized battery to improve the feasibility (brief computerized cognitive assessment (BCCAMS)) combining the CSCT and a computerized test of visual episodic memory. Purpose: to establish the screening value of a brief computerized cognitive assessment (BCCAMS) combining the computerized speed cognitive test (CSCT) and a new computerized episodic visual memory test (CEVMT) in French-speaking patients with multiple sclerosis as compared to a reference battery (MACFIMS).

Interventions

* Questionnaires for assessment of confounding factors * Cognitive evaluation * Walking tests and 9 Hole Peg Test

BEHAVIORALExpanded Disability Status Scale (EDSS) score

\- EDSS score

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER
Bayer
CollaboratorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

Patients : * Aged 18-64 years * Francophone * MS Relapsing-remitting under interferon beta-1b treatment in inclusion, Secondary progressive and Primary progressive MS forms * Having signed an informed consent (later than the day of inclusion and before any examination required by research) * Being affiliated to health insurance Controls: * Aged 18-64 years * Francophone * Having signed an informed consent (later than the day of inclusion and before any examination required by research) * Being affiliated to health insurance

Exclusion criteria

Patients: * Other neurological diseases with impact on cognitive functions. * Severe psychiatric disease or severe depression. * Current Dependence on alcohol or drugs. * Modification or stop of psychotropic treatment in less than a month. * Modification of MS treatment in less than a month. * Visual, visual-motor and / or motor impairments excluding the ability to perform cognitive tests. * Pregnant Controls: * Neurologic disease and known chronic systemic with impact on cognitive functions. * Severe psychiatric disease or severe depression. * Current Dependence on alcohol or drugs. * Psychotropic treatment * Cognitive complaint * Prior cognitive testing with the same tests less than one year. * Pregnant

Design outcomes

Primary

MeasureTime frameDescription
Prediction by the z score BCCAMS of cognitive impairment (at least two tests MACFIMS battery <1.5 SD of control subjectsAt the inclusion (Day 0)average z scores of CEVMT and CSCT

Secondary

MeasureTime frameDescription
Determine values of neuropsychological tests in healthy according to age subjects, gender and the level educationAt the inclusion (Day 0) and at 1 and 6 months after the inclusion (Day 0)BCCAMS and MACFIMS
Ability of the CEVMT to detect episodic memory deficiencies in patients with multiple sclerosis, as compared to established tests of episodic memoryAt the inclusion (Day 0) and at 1 and 6 months after the inclusion (Day 0)California verbal learning test-II and brief-visual memory test-revised
Correlation between alternate forms of the CEVMT and the Brief visual memory test-revised (BVMT-R)At the inclusion (Day 0) and at 1 and 6 months after the inclusion (Day 0)congnitive test
Prediction between cognitive impairment and occupational status/leisure activitiesAt the inclusion (Day 0) and 6 months after the inclusion (Day 0)questionnaire
Effect of possible confounders on results of cognitive testing, including depression, mood, anxiety and fatigueAt the inclusion (Day 0) and at 1 and 6 months after the inclusion (Day 0)scale
Reproducibility of CSCT, CEVMT and the symbol-digit modalities test in clinical settings in patients with multiple sclerosisAt 1 and 6 months after the inclusion (Day 0)congnitive test

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026