CClinicalTrials.gg
CompletedNCT02708927EMOSOCIAL-MSUpdated Aug 27, 2026

Emotional Processing, Family Life, Friendship and Social Integration in Patients With Multiple Sclerosis

An interventional study of Clinical evaluation and Cognitive evaluation in Multiple Sclerosis, sponsored by University Hospital, Bordeaux. Completed at 2 sites in France. Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-27.

Sponsored by University Hospital, Bordeaux · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
91
Allocation
Non-randomized
Ages
18 Years to 45 Years
Sex
All
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Study summary

In addition to the physical, cognitive and psychological symptoms experienced by individuals with Multiple Sclerosis (MS), there is new research which indicates that some individuals with MS have a deficit in emotional processing, specifically, facial affect recognition. Emotional processing is defined as "a central aspect of social cognition". Models of social cognition indicate that emotional processing is an essential component of interpersonal relationships. The failure to accurately perceive other's emotions has been shown to lead to difficulty in social relationships, misinterpreting other's affect, and consequently, inappropriate responding.

However, even though a significant number of individuals with MS have impairments in emotional processing, we do not yet have an understanding of how these impairments affect the social functioning of individuals with MS, including the impact of these deficits on family structure. It is well-known that MS impacts one's social functioning including factors such as employment, daily living activities and interpersonal relationships. Recently a strong correlation was observed between reduced social participation in MS and quality of life. There is evidence to suggest that emotional processing deficits lie at the heart of this reduced social participation in persons with MS, leading to decreased social functioning and thus reduced quality of life. However, to date, this hypothesis has not been tested.

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Conditions studied

  • Multiple Sclerosis

Keywords

  • social integration
  • cognitive impairment
  • emotional processing
  • quality of life
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In context

Multiple Sclerosis

3,460 studies on the registry are indexed under Multiple Sclerosis; 661 are open to participants now.

This study's enrollment of 91 is above the median of 50 across 2,342 interventional studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

University Hospital, Bordeaux is the lead sponsor of 783 studies on the registry; 188 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria (patient group):

  • Age 18-45 years;
  • MS diagnosis according to McDonald criteria (Polman et al., 2005);
  • RRMS;
  • Disease duration \< 15 years;
  • Fluent French speaker;
  • Have a significant other (family members or close friends) who was willing to complete the informant questionnaire BAFQ;
  • Being affiliated to health insurance;
  • Having signed an informed consent (later than the day of inclusion and before any examination required by research).

Inclusion Criteria (healthy control):

  • Age 18-45 years
  • Fluent French speaker;
  • Have a significant other (family members or close friends) who was willing to complete the informant questionnaire BAFQ.
  • Being affiliated to health insurance
  • Having signed an informed consent (later than the day of inclusion and before any examination required by research)

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;
  • 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 three month;
  • change of psychotropic drug since less than one month;
  • Prior neuropsychological testing with the same tests less than one year prevents the participant to participate at this study.
  • Illiteracy, is unable to count or to read;
  • Being under guardianship.
  • Pregnant or breastfeeding women;

Exclusion Criteria (healthy control):

  • History of neurological disease;
  • family history of MS;
  • psychiatric comorbidity including severe depression according to DSMIV;
  • alcohol or other toxic addiction;
  • usage of psychotropic drugs;
  • Known cognitive complaint or neuropsychological affection;
  • Prior neuropsychological testing with the same tests less than one year prevents the participant to participate at this study.
  • Illiteracy, is unable to count or to read;
  • Being under guardianship.
  • Pregnant or breastfeeding women;
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Study design

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

Study arms

  • Experimental
    patient

    MS diagnosis according to McDonald criteria (Polman et al., 2005). Relapsing-remitting MS (RRMS) according to Lublin et al. (1996);

    Other: Clinical evaluation · Other: Cognitive evaluation

  • Experimental
    Control

    healthy subject

    Other: Cognitive evaluation

Interventions

  • OtherClinical evaluation

    • Clinical assessment : Expanded Disability Status Scale (EDSS), ambulation test. Medications will be recorded.

  • OtherCognitive evaluation

    • Neuropsychological, psychological, social and social cognitive evaluation

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What researchers measure

Primary outcomes

  1. Interaction between measures of emotional processing (z score) and functional measures of social interaction

    among the 3 groups (impaired MS, no impaired MS and HS)

    Time frame: At inclusion (day 0)

Secondary outcomes

  1. Correlation between measures of emotional processing with cognitive testing (z scores by domain) and cognitive functioning evaluated by significant other

    (BAFQ)

    Time frame: At inclusion (day 0)

  2. Correlation between measures of emotional processing and quality of life measures

    (MUSIQoL questionnaire).

    Time frame: At inclusion (day 0)

  3. Impact of the cognitive impairment on the relationship of emotional processing (z score) with interpersonal relationships (family, friendship, marital) and society integration and social functioning.

    Time frame: At inclusion (day 0)

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Study locations

2 sites
  • CHU de Bordeaux
    Bordeaux, 33000, France
  • CHU de Dijon
    Dijon, 21079, France
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References and documents

Publications

  • Brochet B, Moreau T, Saubusse A, Charre-Morin J, Lamargue D, Deloire M, Ruet A. Episodic memory deficits are associated with social cognitive impairments in multiple sclerosis. J Neurol. 2026 Aug 20;273(9):534. doi: 10.1007/s00415-026-14067-7. PubMed 42622682 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02708927
Lead sponsor
University Hospital, Bordeaux
Collaborators
FONDATION POUR L'AIDE A LA RECHERCHE SUR LA SCLEROSE EN PLAQUES
Responsible party
Sponsor
First posted
Mar 15, 2016
Start date
Mar 3, 2016
Primary completion
Jan 28, 2019
Completion
Jan 28, 2019
Last update
Aug 27, 2026

Study contacts

Bruno BROCHET, Prof
principal investigator · University Hospital, Bordeaux

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2019. You cannot join it, but the record below documents what was studied.

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