Impact of Sensory, Motor and Vestibular Deficit on the Postural Stability of CMT Patients

NCT ID: NCT06425952

Last Updated: 2024-05-24

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 60 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-05-01
• Study Completion Date: 2026-05-30

Brief Summary

Charcot-Marie-Tooth (CMT), a therapeutically orphan neuromuscular disease affecting one in 2,500 people, represents a challenge to the medical and scientific communities. Physiotherapeutic-rehabilitative strategies play a crucial role in the management of CMT, particularly addressing balance impairment, a key disabling symptom. However, clinical studies in this field are limited. Our study aims to investigate the impact of strengh and somatosensory deficits on static and dynamic balance in CMT patients. The Investigators also aim to explore the involvement of the vestibular system and its correlation with postural instability. Furthermore, the Investigators seek to evaluate relationships between neurochemical biomarkers offering valuable insights for future targeted clinical studies.

Detailed Description

A total of 60 patients will be recruited. To ensure adequate representation of the subgroups of interest, 10 patients with CMT1A (PMP22 gene duplication) and 10 patients with CMT2, regardless of their genotype, will be included. Additionally, three control groups, each comprising 10 subjects, will be included. The first group will consist of patients with motor symptoms, including those with hereditary motor neuropathy (HMN, 10 patients) or distal myopathy (MD, 10 patients). The second group will include patients with solely sensory symptoms, genetic neuropathies, or purely sensory acquired neuropathies such as HSN and neuropathies from anti-MAG antibodies. Finally, the third group will be composed of 10 healthy subjects. Each control subject will have comparable level of disability (motor or somatosensory), age, and gender to the enrolled CMT patients.

All participants must meet the following inclusion criteria to take part in the study:

• Age 18 years or older
• Subject has documented diagnosis of one of the following diseases (except from healthy controls):

• Hereditary sensory-motor neuropathy (CMT) confirmed by genetic analysis
• Hereditary motor neuropathy (HMN) confirmed by genetic analysis
• Hereditary sensory neuropathy (HSN) confirmed by genetic analysis
• Hereditary distal myopathy (MD) confirmed by genetic analysis
• Acquired sensory neuropathy: anti-MAG antibody neuropathy confirmed by neurophysiological, clinical and serological assessment.

The presence of any one of the following exclusion criteria will lead to the exclusion of the subject:

• Inability to maintain an upright position without assistance
• Presence of systemic, neurological (except for the neuropathies and hereditary myopathies under study), psychiatric, orthopedic or rheumatological diseases that may affect evaluation
• Mini Mental State Examination (MMSE)14 score less than 28
• History of alcohol or substance abuse
• Partecipation in intensive motor rehabilitation programs in the last three months.

Conditions

Hereditary Neuropathy

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

CMT patients

patients with sensory-motor genetic neuropathy

No interventions assigned to this group

Motor patients

Patients with motor genetic neuropathy

No interventions assigned to this group

Sensory patients

Patients with sensory neuropathy

No interventions assigned to this group

Myopathic patients

Patients with distal myopathy

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• CMT or HMN or sensory neuropathy or distal myopathy

Exclusion Criteria

• unable to stand
• other neurological, psychiatric, or orthopedic disorders
• MMSE <28
• alcohol abuse
• intensive rehabilitation program

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

IRCCS San Raffaele

OTHER

Sponsor Role: lead

Responsible Party

Stefano Previtali

Head Neuromuscular Repair Unit

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Stefano C Previtali, MD

Role: PRINCIPAL_INVESTIGATOR

IRCCS Ospedale San Raffaele

Locations

Dept. of Neurology, IRCCS Ospedale San Raffaele

Milan, , Italy

Site Status: RECRUITING

Countries

Italy

Central Contacts

Stefano C Previtali, MD

Role: CONTACT

neuromuscolare@hsr.it

00390226433036

Benedetta Sorrenti, MD

Role: CONTACT

neuromuscolare@hsr.it

00390226433036

Facility Contacts

Stefano C Previtali, MD

Role: primary

neuromuscolare@hsr.it

00390226433036

Benedetta Sorrenti, MD

Role: backup

neuromuscolare@hsr.it

00390226433036

Other Identifiers

OSRSCP-EquiCMT

Identifier Type: -

Identifier Source: org_study_id