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Effectiveness of Cryotherapy on the Fatigue of Patients With Multiple Sclerosis (CRYOSEP)

Primary Purpose

Multiple Sclerosis

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
partial-body cryotherapy chamber session
Sponsored by
Fondation Ildys
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring cryotherapy, fatigue, quality of life, spasticity, quality of sleep, depression symptoms

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • men and woen over 18 years old and under 65 years old
  • with multiple sclerosis
  • 0-6 points in the expanded disability states scale (EDSS)
  • with MS in remission (at least 6 months since the last relapse)
  • able to understand and respect the protocol and its requirement
  • who signed the consent prior to any other procedure protocol

Exclusion Criteria:

  • major patients under guardianship/curators/legal protection
  • pregnant patients
  • patients with contraindication for cryotherapy
  • patients unable to complete the entire program
  • patients with substantial change in pharmacological treatment the month before the start of the study

Sites / Locations

  • Centre de PerharidyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Sham Comparator

Sham Comparator

Active Comparator

Active Comparator

Arm Label

Sham cryotherapy full time patient (inpatient)

sham cryotherapy part-time hospitalized patient (outpatient)

cryotherapy full-time hospitalized patient (inpatient)

cryotherapy part-time hospitalized patient (outpatient)

Arm Description

Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-30°C) during their full-time rehabilitation stay

Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-30°C) during their part-time rehabilitation stay

Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-120°C) during their full-time rehabilitation stay

Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-120°C) during their part-time rehabilitation stay

Outcomes

Primary Outcome Measures

Fatigue syndrome
evaluation of the fatigue syndrome using the fatigue severity scale score (FSS). The scale ranges in value from 9 to 63 with high scores indicating the worse outcome.

Secondary Outcome Measures

spasticity symptom
evaluation of the spasticity syndrome using the Ashworth score The scale ranges in value from 0 to 4 with high scores indicating the worse outcome.
quality of Life evaluation
evaluation of the quality of life using the Medical Outcome Study Short Form 36 health survey (MOS-SF36) score. The higher score indicating the better outcome.
pain evaluation
evaluation of pain syndrome using the visual pain scale The scale ranges in value from 0 to 10 with high scores indicating the worse outcome.
quality of sleep
evaluation of sleep quality using the Pittsburgh scale. The scale ranges in value from 0 to 21 with high scores indicating the worse outcome.
depression symptoms
evaluation of depression symptoms using the Beck scale. The scale ranges in value from 0 to 39 with high scores indicating the worse outcome.
physician's global assessment-physical endurance
Evaluation of the 6MWT (6 minutes walk test). High scores indicating the better outcome.
habit changes after rehabilitation stay
Examining habit changes concerning cold therapy after rehabilitation stay using qualitative questionnaire consisting of a small number of direct and meaningful questions (mode and frequency of use).
physician's global assessment-dynamic balance test
Evaluation of the TUG (Time up to go) . High scores indicating the worse outcome.
physician's global assessement-static balance test
Evaluation of the OLS (one leg stance) High scores indicating the better outcome.

Full Information

First Posted
January 7, 2022
Last Updated
September 16, 2022
Sponsor
Fondation Ildys
Collaborators
Lille Catholic University
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1. Study Identification

Unique Protocol Identification Number
NCT05219201
Brief Title
Effectiveness of Cryotherapy on the Fatigue of Patients With Multiple Sclerosis
Acronym
CRYOSEP
Official Title
Effectiveness of Partial-body Cryotherapy on the Fatigue of Patients With Multiple Sclerosis During Readaptation Stay
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 12, 2022 (Actual)
Primary Completion Date
March 2023 (Anticipated)
Study Completion Date
June 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Ildys
Collaborators
Lille Catholic University

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
the aim of the study is to evaluate the effectiveness of partial-body cryotherapy (PBC) on the symptoms of patients with multiple sclerosis during a rehabilitation stay.
Detailed Description
Multiple sclerosis (MS) is a chronic heterogeneous disease with an unpredictable clinical course. Symptoms can include paralysis, ataxia, spasticity, incontinence and fatigue syndrome. Fatigue is considered to be the most prevalent and disabling of the symptoms at all stages of the illness and its occurs in 70-80% of patients. This characteristic of the disease directly impacts the quality of life of patients, affecting their social and physical well being. Physical rehabilitation is often prescribed in the management of MS, and is recognized to improve modifiable impairments in MS. However, the benefit of physical activities may be limited by heat stress also named Uhthoff syndrome frequently observed in patients with MS. Cryotherapy is commonly used as a method to relieve pain and inflammation without marked side effect in respect to contraindication. However well designed studies on PBC in patients with MS are still too sparse. The investigators propose to evaluate the effectiveness of PBC on the symptoms of MS patients during a rehabilitation stay in out- or inpatients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
cryotherapy, fatigue, quality of life, spasticity, quality of sleep, depression symptoms

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sham cryotherapy full time patient (inpatient)
Arm Type
Sham Comparator
Arm Description
Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-30°C) during their full-time rehabilitation stay
Arm Title
sham cryotherapy part-time hospitalized patient (outpatient)
Arm Type
Sham Comparator
Arm Description
Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-30°C) during their part-time rehabilitation stay
Arm Title
cryotherapy full-time hospitalized patient (inpatient)
Arm Type
Active Comparator
Arm Description
Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-120°C) during their full-time rehabilitation stay
Arm Title
cryotherapy part-time hospitalized patient (outpatient)
Arm Type
Active Comparator
Arm Description
Patients benefiting from 15 session of "sham" partial-body cryotherapy session (-120°C) during their part-time rehabilitation stay
Intervention Type
Device
Intervention Name(s)
partial-body cryotherapy chamber session
Other Intervention Name(s)
CRYO00002 ICE X- Cryosauna, local cryotherapy devices DM Class IIb
Intervention Description
The cryotherapy procedure consisted of a 2-3 min stay in the cryotherapy chamber: at -30°C for sham cryotherapy session at -120°C for cryotherapy intervention session. For Inpatients, cryotherapy session will be performed daily, late in the afternoon, excluding saturdays and sundays, during 3 weeks. (15 sessions) For outpatient, cryotherapy session will occured late in the afternoon each day care (15 sessions).
Primary Outcome Measure Information:
Title
Fatigue syndrome
Description
evaluation of the fatigue syndrome using the fatigue severity scale score (FSS). The scale ranges in value from 9 to 63 with high scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks (T1), and 1 month (T2), 3 months (T3) and 1 year (T4) after hospitalization
Secondary Outcome Measure Information:
Title
spasticity symptom
Description
evaluation of the spasticity syndrome using the Ashworth score The scale ranges in value from 0 to 4 with high scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks (T1), and 1 year (T4) after hospitalization
Title
quality of Life evaluation
Description
evaluation of the quality of life using the Medical Outcome Study Short Form 36 health survey (MOS-SF36) score. The higher score indicating the better outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks(T1), and 1 month (T2), 3 months (T3) and 1 year (T4) after hospitalization
Title
pain evaluation
Description
evaluation of pain syndrome using the visual pain scale The scale ranges in value from 0 to 10 with high scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks(T1), and 1 month (T2), 3 months (T3) and 1 year (T4) after hospitalization
Title
quality of sleep
Description
evaluation of sleep quality using the Pittsburgh scale. The scale ranges in value from 0 to 21 with high scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks(T1), after 1 month (T2), 3 months (T3) and 1 year (T4)
Title
depression symptoms
Description
evaluation of depression symptoms using the Beck scale. The scale ranges in value from 0 to 39 with high scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks(T1), and 1 month (T2), 3 months (T3) and 1 year (T4) after hospitalization
Title
physician's global assessment-physical endurance
Description
Evaluation of the 6MWT (6 minutes walk test). High scores indicating the better outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks (T1), and 1 year (T4) after hospitalization
Title
habit changes after rehabilitation stay
Description
Examining habit changes concerning cold therapy after rehabilitation stay using qualitative questionnaire consisting of a small number of direct and meaningful questions (mode and frequency of use).
Time Frame
change from baseline (T0) to 1 month (T2), 3 months (T3) and 1 year (T4) after hospitalization
Title
physician's global assessment-dynamic balance test
Description
Evaluation of the TUG (Time up to go) . High scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks (T1), and 1 year (T4) after hospitalization
Title
physician's global assessement-static balance test
Description
Evaluation of the OLS (one leg stance) High scores indicating the better outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks (T1), and 1 year (T4) after hospitalization
Other Pre-specified Outcome Measures:
Title
Evaluation of cryotherapy effectiveness on fatigue syndrome in accordance to hospitalisation pattern
Description
Primary outcome will be analyzed separately in outpatient versus inpatient in order to determine whether hospitalisation pattern may impact the effectiveness of cryotherapy on fatigue. evaluation of the fatigue syndrome using the fatigue severity scale score (FSS). The scale ranges in value from 9 to 63 with high scores indicating the worse outcome.
Time Frame
change from baseline (T0) to discharge between 3 to 5 weeks (T1)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: men and woen over 18 years old and under 65 years old with multiple sclerosis 0-6 points in the expanded disability states scale (EDSS) with MS in remission (at least 6 months since the last relapse) able to understand and respect the protocol and its requirement who signed the consent prior to any other procedure protocol Exclusion Criteria: major patients under guardianship/curators/legal protection pregnant patients patients with contraindication for cryotherapy patients unable to complete the entire program patients with substantial change in pharmacological treatment the month before the start of the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthieu Pichelin
Phone
02.98.02.85.00
Email
matthieu.pichelin@ildys.org
First Name & Middle Initial & Last Name or Official Title & Degree
Marion Buyse, PhD, PharmD
Phone
0298293447
Email
marion.buyse@ildys.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Baptiste Bourseul, MD
Organizational Affiliation
Fondation Ildys
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre de Perharidy
City
Roscoff
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jocelyne PENGAM
Email
jocelyne.pengam@ildys.org
First Name & Middle Initial & Last Name & Degree
Morgane AUFFRET
Email
morgane.auffret@ildys.org
First Name & Middle Initial & Last Name & Degree
Jean-Sebastien BOURSEUL, MD
First Name & Middle Initial & Last Name & Degree
Joseph BOU LAHDOU, MD
First Name & Middle Initial & Last Name & Degree
Tanguy LE CORRE, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30968613
Citation
Pawik M, Kowalska J, Rymaszewska J. The effectiveness of whole-body cryotherapy and physical exercises on the psychological well-being of patients with multiple sclerosis: A comparative analysis. Adv Clin Exp Med. 2019 Nov;28(11):1477-1483. doi: 10.17219/acem/104529.
Results Reference
background
PubMed Identifier
27712663
Citation
Bouzigon R, Grappe F, Ravier G, Dugue B. Whole- and partial-body cryostimulation/cryotherapy: Current technologies and practical applications. J Therm Biol. 2016 Oct;61:67-81. doi: 10.1016/j.jtherbio.2016.08.009. Epub 2016 Aug 27.
Results Reference
background
PubMed Identifier
33386821
Citation
Radecka A, Knyszynska A, Luczak J, Lubkowska A. Adaptive changes in muscle activity after cryotherapy treatment: Potential mechanism for improvement the functional state in patients with multiple sclerosis. NeuroRehabilitation. 2021;48(1):119-131. doi: 10.3233/NRE-201535.
Results Reference
background
PubMed Identifier
33171768
Citation
Zielinska-Nowak E, Wlodarczyk L, Kostka J, Miller E. New Strategies for Rehabilitation and Pharmacological Treatment of Fatigue Syndrome in Multiple Sclerosis. J Clin Med. 2020 Nov 7;9(11):3592. doi: 10.3390/jcm9113592.
Results Reference
background
PubMed Identifier
26778452
Citation
Miller E, Kostka J, Wlodarczyk T, Dugue B. Whole-body cryostimulation (cryotherapy) provides benefits for fatigue and functional status in multiple sclerosis patients. A case-control study. Acta Neurol Scand. 2016 Dec;134(6):420-426. doi: 10.1111/ane.12557. Epub 2016 Jan 18.
Results Reference
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Effectiveness of Cryotherapy on the Fatigue of Patients With Multiple Sclerosis

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