Safety and Efficacy of the Atalante Exoskeleton in the Rehabilitation of Patients With Amyotrophic Lateral Sclerosis: Study Protocol for an Open, Uncontrolled Interventional Study, EXALS.

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Using a MRI gait motor imagery paradigm in ALS patients in order to study how ALS affects the function of the central neural networks involved in gait function, we showed a reorganization of the motor networks that represents a compensatory response to the dysfunction of the networks involved in gait function. Our main hypothesis is that by providing coherent proprioceptive input to the sensorimotor integration areas, gait training with an exoskeleton may boost compensatory network reorganization and help to maintain function. We hypothesize that this can be achieved through a locomotion training strategy that reproduces normal gait motor patterns and appropriate sensory feedback. Gait training with an exoskeleton can meet these needs. The Atalante exoskeleton offers unique potential thanks to its cutting-edge technological features, hands-free functions and availability in numerous centers across Europe. Evaluation of its safety and efficacy in ALS is of the utmost interest in order to generalize this new approach in ALS.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• Patients with amyotrophic lateral sclerosis (defined according to the El Escorial criteria: possible, probable or definite), at the time of diagnosis

• Male or female, between 18 and 70 years of age

• Slowly and moderately evolving patients ∆ ALS Progression rate (FS) ≤ 1.11 (The ALS progression rate was calculated as follows: (48 - ALSFRS-R at screening visit) / (duration from onset to this visit (month)) (Kimura et al., 2006). ALSFRS-R progression will be classified as slow (∆FS ≤ 0.47), intermediate (0.47 ≤ ∆PR ≤1.11) or fast (∆PR \> 1.11) (Labra et al., 2016).

• Manual muscle testing ≥ 3 for deltoid muscle and ≥ 4 for neck flexors and extensors muscles

• Ambulatory status: a stable gait deficit with a total score between 3 and 6 on the ALSFRS-R sub-items walking and climbing stairs

• French speaking patient

• Patient affiliated with the French social security system

• Signed informed consent

• Measurements related to the use of the Atalante exoskeleton:

• Height between 155 and 190 cm

• Weight \< 90 kg

• Pelvis width \< 46 cm in seated position

• Thigh length between 56.8 and 64.8 cm

• Leg length \> 45.7cm or less than:

• 60.7cm if ankle dorsi flexion is ≥16°

• 57.7cm if ankle dorsi flexion is ≥13°and \<16°

• Joint amplitudes of lower limbs :

• Hip: flexion 90°, extension 5°, medial rotation 10°, lateral rotation 20°, abduction 17°, adduction 10°

• Knee: flexion 5-110°

• Ankle: dorsiflexion (knee straight) 0°, plantarflexion 9°, eversion18°, inversion 18°.

Locations
Other Locations
France
Hôpital Pitié-Salpêtrière
RECRUITING
Paris
Institut de myologie
RECRUITING
Paris
Station Debout
RECRUITING
Paris
Contact Information
Primary
Ghida TRAD, PhD
ghida.trad@inserm.fr
01 42 17 62 05
Backup
Pierre-François PRADAT, MD, PhD
pierre-francois.pradat@aphp.fr
Time Frame
Start Date: 2024-01-31
Estimated Completion Date: 2027-01-29
Participants
Target number of participants: 20
Treatments
Other: Patient
Single-group study following an ABA design:~Phase A1 (usual care for 6 weeks) Phase B (usual care + gait training using exoskeleton for 6 weeks) Phase A2 (usual care for 6 weeks) All participants undergo the same sequence of conditions according to the protocol.
Sponsors
Collaborators: Institut de Myologie, France, Station Debout, Laboratory of Biomedical Imaging, Association pour la Recherche sur la Sclérose Latérale Amyotrophique et autres Maladies du Motoneurone, Groupe Hospitalier Pitie-Salpetriere
Leads: Institut de Recherche sur la Moelle épinière et l'Encéphale

This content was sourced from clinicaltrials.gov