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Treadmill, Stretching and Proprioceptive Exercise (TreSPE) Rehabilitation Program for Charcot-Marie-Tooth Neuropathy Type 1A (CMT1A) (TreSPE)

Primary Purpose

Charcot-Marie-Tooth Disease, Charcot-Marie-Tooth Disease Type 1A

Status
Unknown status
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
TreSPE
SPE
Sponsored by
University of Genova
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Charcot-Marie-Tooth Disease focused on measuring Charcot-Marie-Tooth disease,, CMT1A,, rehabilitation,, treadmill,, stretching,, proprioception,, Randomised Controlled Trial.

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Clinical diagnosis of CMT1A
  • Genetic confirmation (17p112 chromosome duplication)
  • Age 18 - 70 years old
  • Ability to accomplish the primary outcome measure (10 meter walking test) without support, with or without ankle foot orthoses (AFO)
  • Ability to walk on a treadmill on a horizontal plane for 20 minutes at a speed of 1.5 km/h with or without support at the bars
  • Score at the Mobility Scale between 2 and 11
  • Signed written informed consent to participate

Exclusion Criteria:

  • Diagnosis of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) or any other type of CMT
  • Other associated causes of neuropathy
  • Vestibular affections, psychiatric, cardiovascular and lung disorders or severe arthropathic changes in the lower limbs
  • Non ambulating patients or patients always requiring even monolateral support to walk
  • Other neurological disorders

Sites / Locations

  • University of Genoa
  • I.R.C.C.S. Foundation, Besta Institute
  • Don Carlo Gnocchi Foundation
  • Departement of Neurological and Visual Sciences, University of Verona

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TreSPE

SPE

Arm Description

Treatment with treadmill, proprioceptive and stretching exercises

Proprioceptive and stretching exercises

Outcomes

Primary Outcome Measures

Walking ability of patients will be evaluated as the time needed to walk for 10 meters at normal speed for the patients
The walking ability of patients will be evaluated through the "10 meters timed walk test" which will be performed at baseline (T1 or day-1), at the end of the three months of treatment (T2 or day90) and at the end of the three months of follow up (T3 or day180).
Walking ability of patients will be evaluated after finishing the treatment as the time needed to walk for 10 meters at normal speed for the patients
The walking ability of patients will be evaluated through the "10 meters timed walk test" which will be performed at baseline (T1 or day-1), at the end of the three months of treatment (T2 or day90) and at the end of the three months of follow up (T3 or day180).
Walking ability of patients will be evaluated after finishing the treatment as the time needed to walk for 10 meters at normal speed for the patients
The walking ability of patients will be evaluated through the "10 meters timed walk test" which will be performed at baseline (T1 or day-1), at the end of the three months of treatment (T2 or day90) and at the end of the three months of follow up (T3 or day180).

Secondary Outcome Measures

Balance will be evaluated through the Berg Scale
The Berg scale is a tool to evaluate balance and ranges from 0 to 36 points being 36 normal
Balance will be evaluated through the Berg Scale
The Berg scale is a tool to evaluate balance and ranges from 0 to 36 points being 36 normal
balance will be evaluted through the Berg scale
The Berg scale is a tool to evaluate balance and ranges from 0 to 36 points being 36 normal
Quality of life will be evaluated through the SF - 36 questionnaire
The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index.
Quality of life will be evaluated through the SF - 36 questionnaire
The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index.
Quality of life will be evaluated through the SF - 36 questionnaire
The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index.

Full Information

First Posted
January 24, 2011
Last Updated
February 3, 2011
Sponsor
University of Genova
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1. Study Identification

Unique Protocol Identification Number
NCT01289704
Brief Title
Treadmill, Stretching and Proprioceptive Exercise (TreSPE) Rehabilitation Program for Charcot-Marie-Tooth Neuropathy Type 1A (CMT1A)
Acronym
TreSPE
Official Title
A Multicenter Study to Evaluate the Effects on Charcot-Marie-Tooth Neuropathy Type 1A of a Composite Treadmill, Stretching and Proprioceptive Exercise (TreSPE) Rehabilitation Program.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2010
Overall Recruitment Status
Unknown status
Study Start Date
February 2011 (undefined)
Primary Completion Date
October 2011 (Anticipated)
Study Completion Date
January 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Genova

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Charcot-Marie-Tooth neuropathy type 1A (CMT1A) is one of the most common inherited neurological disorders. The study will evaluate the efficacy and safety of an innovative rehabilitation protocol constituted by exercises at the treadmill and by a stretching and proprioceptive approach. A total of 92 patients will be enrolled in the study and treated in a controlled, randomized, single blind, way. To recruit a high number of patients with CMT1A the study will be multicentric and will comprehend four of the most active clinical centers in the field of CMT, in Italy. People with CMT1A are very motivated in entering rehabilitation protocols because to date there is no effective therapy for this disease. Therefore, the investigators expect a high compliance by the patients. With the present project the investigators plan to clarify several unanswered questions: 1) the efficacy and safety of treadmill over a more conventional protocol; 2) the duration and frequency of any rehabilitation treatment; 3) the most sensitive outcome measures to evaluate the efficacy of rehabilitation approach in patients with CMT.
Detailed Description
A multicentre, prospective, randomised, controlled, single blind study to evaluate the impact of aerobic exercise, based on a tightly controlled program at the treadmill, on the rehabilitation therapy of CMT 1A neuropathy. Comparing aerobic training at the treadmill combined with respiratory physiotherapy, stretching and proprioceptive exercises (TreSPE- treated group) with a more conventional treatment only composed by respiratory physiotherapy, stretching and proprioceptive exercises (SPE- control group) will provide information on the impact of Treadmill in CMT1A. 92 patients (23 per centre) will be enrolled and randomly assigned to TreSPE (n = 46) or to SPE (n = 46). Both groups will be treated for three months and followed up for six months. No serious side effects are expected with TreSPE, as also suggested by our preliminary results. For safety reasons blood pressure (BP), heart rate (HR) and an electrocardiogram will be recorded during the rehabilitation treatment when the treating physician considers it necessary. The patients will be allowed, if needed, to hold at the parallel bars of the treadmill during exercise. According to the American Thoracic Society (ATS) guidelines the cardiopulmonary exercise test will be interrupted if BP raises at 240/120 and/or HR to 220-patients age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Charcot-Marie-Tooth Disease, Charcot-Marie-Tooth Disease Type 1A
Keywords
Charcot-Marie-Tooth disease,, CMT1A,, rehabilitation,, treadmill,, stretching,, proprioception,, Randomised Controlled Trial.

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
92 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TreSPE
Arm Type
Experimental
Arm Description
Treatment with treadmill, proprioceptive and stretching exercises
Arm Title
SPE
Arm Type
Active Comparator
Arm Description
Proprioceptive and stretching exercises
Intervention Type
Other
Intervention Name(s)
TreSPE
Other Intervention Name(s)
SPE
Intervention Description
treadmill: 5'warm up, 20'aerobic exercise (gradually incremented to 30', from session to session, if possible), 5'warm down, controlling hearth rate, blood pressure and SaO2. Respiratory Physiotherapy: positive Expiratory Pressure (PEP) bottle for 10' (in various postures), and postural training, for the other 10'. Stretching for 20', of the triceps surae, tibialis posterior, extensor and flexors digitorum longus and brevis, both at the bed and in a static position. Proprioceptive and postural kinesitherapy according to the Perfetti method. Balance Exercising consists of exercises carried on by basculating bars with improving difficulties in the instruments utilized and in the tasks with therapist supervision and near a handbar preventing falls.
Intervention Type
Other
Intervention Name(s)
SPE
Intervention Description
Respiratory Physiotherapy for 20', consisting of Positive Expiratory Pressure (PEP) bottle for 10' (in various postures), and postural training according to the Mèzières technique, for the other 10'. Stretching for 20', of the triceps surae, tibialis posterior, extensor and flexors longus and brevis, both at the bed and in a static position. Proprioceptive and postural kinesitherapy according to the neurocognitive method. Balance Exercising consists of exercises carried on by moving bars with improving difficulties in the instruments utilized and in the tasks with therapist supervision and near a handlebar preventing falls.
Primary Outcome Measure Information:
Title
Walking ability of patients will be evaluated as the time needed to walk for 10 meters at normal speed for the patients
Description
The walking ability of patients will be evaluated through the "10 meters timed walk test" which will be performed at baseline (T1 or day-1), at the end of the three months of treatment (T2 or day90) and at the end of the three months of follow up (T3 or day180).
Time Frame
Baseline: 1 day before the rehabilitative protocol starts (T1)
Title
Walking ability of patients will be evaluated after finishing the treatment as the time needed to walk for 10 meters at normal speed for the patients
Description
The walking ability of patients will be evaluated through the "10 meters timed walk test" which will be performed at baseline (T1 or day-1), at the end of the three months of treatment (T2 or day90) and at the end of the three months of follow up (T3 or day180).
Time Frame
at the end of treatment: day 90 (T2)
Title
Walking ability of patients will be evaluated after finishing the treatment as the time needed to walk for 10 meters at normal speed for the patients
Description
The walking ability of patients will be evaluated through the "10 meters timed walk test" which will be performed at baseline (T1 or day-1), at the end of the three months of treatment (T2 or day90) and at the end of the three months of follow up (T3 or day180).
Time Frame
at the end of follow up: day 180 (T3)
Secondary Outcome Measure Information:
Title
Balance will be evaluated through the Berg Scale
Description
The Berg scale is a tool to evaluate balance and ranges from 0 to 36 points being 36 normal
Time Frame
Baseline: 1 day before the rehabilitative protocol starts
Title
Balance will be evaluated through the Berg Scale
Description
The Berg scale is a tool to evaluate balance and ranges from 0 to 36 points being 36 normal
Time Frame
at the end of treatment: day 90 (T2)
Title
balance will be evaluted through the Berg scale
Description
The Berg scale is a tool to evaluate balance and ranges from 0 to 36 points being 36 normal
Time Frame
at the end of follow up: day 180 (T3)
Title
Quality of life will be evaluated through the SF - 36 questionnaire
Description
The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index.
Time Frame
Baseline: 1 day before the rehabilitative protocol starts (T1)
Title
Quality of life will be evaluated through the SF - 36 questionnaire
Description
The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index.
Time Frame
at the end of treatment: day 90 (T2)
Title
Quality of life will be evaluated through the SF - 36 questionnaire
Description
The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index.
Time Frame
at the end of follow up: day 180 (T3)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of CMT1A Genetic confirmation (17p112 chromosome duplication) Age 18 - 70 years old Ability to accomplish the primary outcome measure (10 meter walking test) without support, with or without ankle foot orthoses (AFO) Ability to walk on a treadmill on a horizontal plane for 20 minutes at a speed of 1.5 km/h with or without support at the bars Score at the Mobility Scale between 2 and 11 Signed written informed consent to participate Exclusion Criteria: Diagnosis of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) or any other type of CMT Other associated causes of neuropathy Vestibular affections, psychiatric, cardiovascular and lung disorders or severe arthropathic changes in the lower limbs Non ambulating patients or patients always requiring even monolateral support to walk Other neurological disorders
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Margherita A Monti Bragadin, MD
Phone
0039-010-3537040
Email
margherita.montibragadin@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Angelo E Schenone, MD
Organizational Affiliation
University of Genova
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Genoa
City
Genoa
ZIP/Postal Code
16132
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angelo Schenone, Professor
Phone
+39 010 353 7040
Email
aschenone@neurologia.unige.it
Facility Name
I.R.C.C.S. Foundation, Besta Institute
City
Milan
ZIP/Postal Code
20133
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Davide Pareyson, MD
Phone
+39 02 23943001
Email
dpareyson@istituto-besta.it
Facility Name
Don Carlo Gnocchi Foundation
City
Rome
ZIP/Postal Code
00194
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luca Padua, MD
Phone
+39 06 33086231
Email
lpadua@rm.unicatt.it
Facility Name
Departement of Neurological and Visual Sciences, University of Verona
City
Verona
ZIP/Postal Code
37134
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gian Maria Fabrizi, MD
Phone
+39 045 8124461
Email
gianmaria.fabrizi@univr.it

12. IPD Sharing Statement

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Links:
URL
http://www.acmt-rete.it
Description
Acmt-Rete is a non-profit organization made by a group of patients to help the CMT community and to promote research in the field of hereditary neuropathies

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Treadmill, Stretching and Proprioceptive Exercise (TreSPE) Rehabilitation Program for Charcot-Marie-Tooth Neuropathy Type 1A (CMT1A)

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