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Efficacy of a Personalized Rehabilitation Program of Facial Involvement in Systemic Sclerosis (PREVISS)

Primary Purpose

Systemic Sclerosis, Face, Facial Involvement

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Personalized rehabilitation program of facial involvement in systemic sclerosis
Delivery of a standard prescription for facial rehabilitation
Sponsored by
University Hospital, Strasbourg, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Systemic Sclerosis focused on measuring Face, Facial involvement, Rehabilitation, Systemic sclerosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 yo
  • Systemic sclerosis according to the 2013 ACR/EULAR (American College of Rheumatology) classification criteria
  • Systemic sclerosis with facial involvement defined by a MHISS score > 6
  • Immunosuppressive and/or anti-fibrosis treatment stable for at least 1 month
  • Subject able to understand the objectives and risks of research and to give informed consent
  • Subject enrolment in the health insurance scheme

Exclusion Criteria:

  • Pregnancy
  • Previous participation in a rehabilitation program of facial involvement
  • Patient under legal protection
  • Impossibility to give clear information of subject

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Other

    Arm Label

    Personalized rehabilitation program of facial involvement in systemic sclerosis

    Routine care

    Arm Description

    3 sessions of 2 hours of facial rehabilitation in hospital over 2 weeks including: Physiotherapy with facial and endo-oral massages, self-massages, active and passive exercises of the face and mouth, tongue exercises Speech therapy with mobilization of the orofacial sphere applied to swallowing and speech difficulties Individual workshop on the theme of dry mouth, dry mouth, swallowing disorders, and oral care Individual therapeutic makeup workshop A motivational interview A patient notebook with a personalized protocol for self-rehabilitation of the face A video tutorial for self-rehabilitation of the face Facial self-rehabilitation sessions at home

    Delivery of a standard prescription for facial rehabilitation

    Outcomes

    Primary Outcome Measures

    Mouth Handicap In Systemic Sclerosis (MHISS) score
    A 12-item questionnaire specifically quantifying mouth disability in systemic sclerosis

    Secondary Outcome Measures

    Mouth Handicap In Systemic Sclerosis (MHISS) score
    A 12-item questionnaire specifically quantifying mouth disability in systemic sclerosis
    Mouth Handicap In Systemic Sclerosis (MHISS) score
    A 12-item questionnaire specifically quantifying mouth disability in systemic sclerosis
    Interincisal distance measurement
    Interincisal distance measurement in mm
    Interincisal distance measurement
    Interincisal distance measurement in mm
    Rodnan skin score on the face
    a measure of skin thickness
    Rodnan skin score on the face
    a measure of skin thickness
    Visual Analog Scale (VAS) for pain
    Visual Analog Scale (VAS) for pain
    Visual Analog Scale (VAS) for pain
    HAQ questionnaire
    Health Assessment Questionnaire
    HAQ questionnaire
    Health Assessment Questionnaire
    SF12 questionnaire (12-item Short Form Survey)
    a 12-item general health questionnaire
    SF12 questionnaire (12-item Short Form Survey)
    a 12-item general health questionnaire
    Weight
    Weight in kg
    Total number of rehabilitation sessions
    Total duration of rehabilitation sessions
    Total number of rehabilitation sessions
    Total duration of rehabilitation sessions

    Full Information

    First Posted
    November 22, 2021
    Last Updated
    August 17, 2022
    Sponsor
    University Hospital, Strasbourg, France
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05177380
    Brief Title
    Efficacy of a Personalized Rehabilitation Program of Facial Involvement in Systemic Sclerosis
    Acronym
    PREVISS
    Official Title
    Efficacy of a Personalized Rehabilitation Program of Facial Involvement in Systemic Sclerosis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2022 (Anticipated)
    Primary Completion Date
    April 2024 (Anticipated)
    Study Completion Date
    April 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University Hospital, Strasbourg, France

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Systemic sclerosis is a rare autoimmune disorder characterized by microangiopathy, activation of the immune system, and sclerosis of tissues including the skin. Facial involvement is frequent and disabling. It causes significant functional and aesthetic discomfort, and a major deterioration in quality of life. It results in a loss of suppleness of the skin and subcutaneous tissues, dysfunction of the temporomandibular joint, peribuccal rhagades, microstomia, and dry mouth causing difficulties in mouth opening, feeding, dental care, and weight loss. Facial involvement in systemic sclerosis can be assessed using the Mouth Handicap in Systemic Sclerosis (MHISS) score, a validated patient questionnaire assessing the functional and aesthetic consequences of systemic sclerosis on the face. Although common and disabling, facial involvement is underestimated and poorly managed. Immunosuppressive and/or anti-fibrosis drugs are not very effective. Facial rehabilitation could significantly improve the mouth handicap but facial rehabilitation is not currently performed in standard care in systemic sclerosis patients. The aim of the study is to evaluate the efficacy of a personalized rehabilitation program vs standard care in facial involvement of systemic sclerosis patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Systemic Sclerosis, Face, Facial Involvement, Rehabilitation
    Keywords
    Face, Facial involvement, Rehabilitation, Systemic sclerosis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Personalized rehabilitation program of facial involvement in systemic sclerosis
    Arm Type
    Experimental
    Arm Description
    3 sessions of 2 hours of facial rehabilitation in hospital over 2 weeks including: Physiotherapy with facial and endo-oral massages, self-massages, active and passive exercises of the face and mouth, tongue exercises Speech therapy with mobilization of the orofacial sphere applied to swallowing and speech difficulties Individual workshop on the theme of dry mouth, dry mouth, swallowing disorders, and oral care Individual therapeutic makeup workshop A motivational interview A patient notebook with a personalized protocol for self-rehabilitation of the face A video tutorial for self-rehabilitation of the face Facial self-rehabilitation sessions at home
    Arm Title
    Routine care
    Arm Type
    Other
    Arm Description
    Delivery of a standard prescription for facial rehabilitation
    Intervention Type
    Procedure
    Intervention Name(s)
    Personalized rehabilitation program of facial involvement in systemic sclerosis
    Intervention Description
    Personalized rehabilitation program of facial involvement in systemic sclerosis
    Intervention Type
    Other
    Intervention Name(s)
    Delivery of a standard prescription for facial rehabilitation
    Intervention Description
    Delivery of a standard prescription for facial rehabilitation
    Primary Outcome Measure Information:
    Title
    Mouth Handicap In Systemic Sclerosis (MHISS) score
    Description
    A 12-item questionnaire specifically quantifying mouth disability in systemic sclerosis
    Time Frame
    Week 6
    Secondary Outcome Measure Information:
    Title
    Mouth Handicap In Systemic Sclerosis (MHISS) score
    Description
    A 12-item questionnaire specifically quantifying mouth disability in systemic sclerosis
    Time Frame
    Week 2
    Title
    Mouth Handicap In Systemic Sclerosis (MHISS) score
    Description
    A 12-item questionnaire specifically quantifying mouth disability in systemic sclerosis
    Time Frame
    Week12
    Title
    Interincisal distance measurement
    Description
    Interincisal distance measurement in mm
    Time Frame
    Week 6
    Title
    Interincisal distance measurement
    Description
    Interincisal distance measurement in mm
    Time Frame
    Week 12
    Title
    Rodnan skin score on the face
    Description
    a measure of skin thickness
    Time Frame
    Week 6
    Title
    Rodnan skin score on the face
    Description
    a measure of skin thickness
    Time Frame
    Week 12
    Title
    Visual Analog Scale (VAS) for pain
    Time Frame
    Week 2
    Title
    Visual Analog Scale (VAS) for pain
    Time Frame
    Week 6
    Title
    Visual Analog Scale (VAS) for pain
    Time Frame
    Week12
    Title
    HAQ questionnaire
    Description
    Health Assessment Questionnaire
    Time Frame
    Week 6
    Title
    HAQ questionnaire
    Description
    Health Assessment Questionnaire
    Time Frame
    Week 12
    Title
    SF12 questionnaire (12-item Short Form Survey)
    Description
    a 12-item general health questionnaire
    Time Frame
    Week 6
    Title
    SF12 questionnaire (12-item Short Form Survey)
    Description
    a 12-item general health questionnaire
    Time Frame
    Week 12
    Title
    Weight
    Description
    Weight in kg
    Time Frame
    Week 12
    Title
    Total number of rehabilitation sessions
    Time Frame
    Week 6
    Title
    Total duration of rehabilitation sessions
    Time Frame
    Week 6
    Title
    Total number of rehabilitation sessions
    Time Frame
    Week 12
    Title
    Total duration of rehabilitation sessions
    Time Frame
    Week 12

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age ≥ 18 yo Systemic sclerosis according to the 2013 ACR/EULAR (American College of Rheumatology) classification criteria Systemic sclerosis with facial involvement defined by a MHISS score > 6 Immunosuppressive and/or anti-fibrosis treatment stable for at least 1 month Subject able to understand the objectives and risks of research and to give informed consent Subject enrolment in the health insurance scheme Exclusion Criteria: Pregnancy Previous participation in a rehabilitation program of facial involvement Patient under legal protection Impossibility to give clear information of subject
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Emmanuel CHATELUS, MD
    Phone
    +33 3 88 12 71 40
    Email
    emmanuel.chatelus@chru-strasbourg.fr

    12. IPD Sharing Statement

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    Efficacy of a Personalized Rehabilitation Program of Facial Involvement in Systemic Sclerosis

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