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Study of Social Cognition by Morphological and Functional Imaging in Multiple Sclerosis Patients (SOCOG-MS)

U

University Hospital of Bordeaux

Status

Completed

Conditions

Multiple Sclerosis

Treatments

Other: Brain MRI - Clinical and cognitive evaluation
Device: MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT02290587
CHUBX 2014/01

Details and patient eligibility

About

In recent years, studies have brought knowledge of the difficulties of social cognition in Multiple Sclerosis (MS). The brain tissue alteration at the origin of these difficulties in social cognition mechanisms remain poorly understood. Although recent behavioral studies indicated social disturbances in many of these patients, functional studies investigating specific theory of mind in MS are lacking. The use of new techniques for morphological and functional Magnetic Resonance Imaging (MRI) can identify brain activation networks, mapping the achievement and tissue integrity may be related to disorders of social cognition and cognitive. The investigators propose to study social cognition in MS patients using morphological and functional imaging to determine the mechanisms underlying phenomena such as cerebral compensation and its relationship with cognitive impairment.

Enrollment

35 patients

Sex

All

Ages

18 to 59 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (patient group):

  • Aged 18-59 years
  • Right handed
  • Fluent French speaker
  • MS diagnosis according to McDonald criteria (Polman et al., 2005).
  • Relapsing-remitting MS (RRMS) according to Lublin et al. (1996);
  • Having signed an informed consent (later than the day of inclusion and before any examination required by research)
  • Being affiliated to health insurance

Inclusion Criteria (healthy control):

  • Aged 18-59 years
  • Right handed
  • Fluent French speaker
  • 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 (patient group):

  • Other progressive neurological disease;
  • psychiatric comorbidity including severe depression according to Diagnostic and Statistical Manual-IV (DSM-IV),
  • alcohol or other addiction to toxic,
  • Expanded Disability Status Scale (EDSS) > 6; disabling visual or motor problems preventing participation to neuropsychological assessments,
  • relapse since less than one month,
  • change of disease-modifying therapy or psychotropic drug since less than one month,
  • Contra-indication to MRI (pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments or foreign objects in the eyes, skin or body, claustrophobia) or refusing MRI
  • Illiteracy, is unable to count or to read
  • Pregnant or breastfeeding women
  • Being under guardianship

Exclusion Criteria (healthy control):

  • History of neurological disease;
  • family history of MS;
  • psychiatric comorbidity including severe depression according to DSM-IV;
  • alcohol or other toxic addiction;
  • psychotropic drugs; known cognitive complaint or neuropsychological affection;
  • Prior neuropsychological testing with the same tests less than one year
  • Contra-indication to MRI (pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments or foreign objects in the eyes, skin or body, claustrophobia) or refusing MRI
  • Illiteracy, is unable to count or to read
  • Pregnant or breastfeeding women
  • Being under guardianship

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

35 participants in 2 patient groups

Patient
Experimental group
Description:
MS diagnosis according to McDonald criteria (Polman et al., 2005). Relapsing-remitting MS (RRMS) according to Lublin et al. (1996);
Treatment:
Other: Brain MRI - Clinical and cognitive evaluation
Device: MRI
Control
Experimental group
Description:
healthy subject
Treatment:
Other: Brain MRI - Clinical and cognitive evaluation
Device: MRI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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