INESEP: The Role of Social and Territorial Inequalities in the Management and Prognosis of Multiple Sclerosis

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Recruiting
CT.gov ID
NCT05017038
Collaborator
(none)
2,000
5
27.9
400
14.3

Study Details

Study Description

Brief Summary

Although the majority of the French population is covered by social security, the effects of social inequalities on health are still very visible and are even increasing in France and in Europe. Thus, according to INSEE, excess mortality is observed among the most disadvantaged populations. Similarly, the prevalence of certain chronic diseases in France and Europe, particularly cardiovascular diseases, is linked to social inequalities and excess morbidity can be observed in the most disadvantaged populations.

In addition to social inequalities, which refer to disparities in health levels according to social category, there are the effects of territorial inequalities. In France, there are geographical areas of excess mortality, which essentially correspond to areas far from urban centers. Similarly, there are major geographical differences in terms of medical supply and equipment, and the distance between patients and health centers is a direct obstacle to the use of the health care network.

The underlying explanations for social inequalities in health are multiple. While it is likely that difficulties in accessing and using care play a role, it is also possible that they are due to differences in exposure to certain environmental (e.g. pollution) or individual (e.g. smoking) risk factors. But it is also possible that the causal relationship is the opposite and that diseases create or reveal social inequalities.

For multiple sclerosis (MS) the impact of social and territorial inequalities is more debated. Indeed, with regard to the relationship between disease prevalence and social inequalities, a recent literature review found 21 separate studies on the subject, of which 13 failed to show a link between socioeconomic status and MS risk, 5 concluded that there was an increased risk of MS in advantaged populations and 3 concluded that there was an increased risk of MS in disadvantaged populations. There are plausible pathophysiological explanations for either direction of the relationship, but the question remains open.

To our knowledge, the link between MS prognosis and social inequalities has been little studied, as disadvantaged populations are more often exposed to the poor prognostic factor of smoking [6-8], the hypothesis of a negative prognostic role of social inequalities remains plausible. Similarly, the current consensus is that the diagnosis and treatment of MS should be as early as possible [9,10] in order to preserve brain capital. Easy access to a neurologist and MRI are therefore potentially prognostic factors for MS in relation to territorial inequalities. It should be noted that the link between social and geographical inequalities and a potential delay in treatment has not been demonstrated in France in the case of cancer, but it is possible that the importance of the means implemented in the fight against cancer erases these effects. In MS, a study showed a link between delay in starting a second disease-modifying therapy and socio-economic status.

While the causal link between MS and socio-professional status has not yet been demonstrated, the socio-economic impact of MS has been measured. In particular, it has been shown that having MS is associated with an increased risk of unemployment and/or early retirement.

The primary objective of our study is to determine whether delay in treatment, as a marker of difficulties in access to care in MS, is associated with social and territorial inequalities in MS. Secondary objectives will be to explore the link between MS prognosis and social and territorial inequalities.

Exposure to sunlight is a known protective factor and is consistent with the north-east-south-west gradient observed in France. The choice of centers associated with the research, spread over the French territory, will make it possible to monitor and measure this effect in the prognosis of MS.

As the available treatments have evolved considerably over the last ten years, and in order to avoid a period effect, the patients recruited in the study will have to have a date of onset of the disease after 1 January 2009.

Primary objective Determining the relationship between socio-economic inequalities and the time to start disease-modifying therapy in MS Secondary objective

  1. To determine the relationship between geographical inequalities and delay in starting disease-modifying therapy in MS

  2. To determine the relationship between socio-economic inequalities and time to walking disability (EDSS 4)

  3. To determine the relationship between geographical inequalities and time to walking disability (EDSS 4)

  4. To measure the impact of disability on socioeconomic status in MS patients

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    2000 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    The Role of Social and Territorial Inequalities in the Management and Prognosis of Multiple Sclerosis - Longitudinal Observational Study - INESEP
    Actual Study Start Date :
    Mar 3, 2021
    Anticipated Primary Completion Date :
    Mar 3, 2023
    Anticipated Study Completion Date :
    Jun 30, 2023

    Outcome Measures

    Primary Outcome Measures

    1. The endpoint will be the time from disease onset to treatment, and the co-variates of the multivariate model will be all socio-demographic and clinical characteristics at disease onset. [The total time for a subject to participate is approximately 25 minutes, while reading the newsletter, asking questions if necessary and completing a questionnaire.]

      The endpoint will be the time from disease onset to treatment, and the co-variates of the multivariate model will be all socio-demographic and clinical

    Secondary Outcome Measures

    1. Delay before first treatment [The total time for a subject to participate is approximately 25 minutes, while reading the newsletter, asking questions if necessary and completing a questionnaire.]

      Delay before first treatment

    2. Time to reach an EDSS of more than 4 [The total time for a subject to participate is approximately 25 minutes, while reading the newsletter, asking questions if necessary and completing a questionnaire.]

      Time to reach an EDSS of more than 4

    3. Difference in disposable income between the start of the illness and the point date. [The total time for a subject to participate is approximately 25 minutes, while reading the newsletter, asking questions if necessary and completing a questionnaire.]

      Difference in disposable income between the start of the illness and the point date.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion criteria

    • Be of legal age

    • Have a confirmed MS according to the McDonald criteria 2017

    • Have the date of onset of the disease recorded in EDMUS

    • Have a disease onset date after 1 January 2009

    • For patients receiving treatment for their MS*: have the date of first disease- modifying therapy entered in EDMUS

    • Patients not receiving treatment for their MS can be included if they meet the other criteria

    Exclusion criteria

    • Being deprived of liberty or under guardianship

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Service de Neurologie et Maladies inflammatoires du Système nerveux central Bordeaux France 33000
    2 Service de Neurologie Clermont-ferrand France 63000
    3 Service de Neurologie Nancy France 54000
    4 Pôle Neurosciences Rennes France 35000
    5 CIC 1433 Épidémiologie CliniqueInserm, CHRU, Université de Lorraine Vandœuvre-les-Nancy France 54511

    Sponsors and Collaborators

    • Central Hospital, Nancy, France

    Investigators

    • Principal Investigator: Marc DEBOUVERIE, PU-PH, Service de Neurologie CHRU de Nancy
    • Principal Investigator: Aurélie RUET, PU-PH, Service de Neurologie et Maladies inflammatoires du systéme nerveux central
    • Principal Investigator: Gilles EDAN, PU-PH, PÔLE NEUROSCIENCES, CHU de Rennes
    • Principal Investigator: Pierre CLAVELOU, PU-PH, Service de Neurologie, CHU de Clermont-Ferrand

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Central Hospital, Nancy, France
    ClinicalTrials.gov Identifier:
    NCT05017038
    Other Study ID Numbers:
    • 2019-A02739-48
    First Posted:
    Aug 23, 2021
    Last Update Posted:
    Aug 23, 2021
    Last Verified:
    Jul 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 23, 2021