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Completed

NCT Number: NCT01435694

Robot-assisted Gait Training in Multiple Sclerosis Subjects

Aims of the study:

This is a randomized-controlled trial to test the effects of robot-assisted gait training on locomotor function and motor unit firing rate in multiple sclerosis subjects with severe gait impairments. The control group will be treat with conventional physical therapy.

Subjects and methods:

60 multiple sclerosis patients will be recruited in two outpatient rehabilitation clinics.

Informed consent will be obtained. Participants will be randomized to Robot-assisted gait training (experimental group) or conventional therapy (control group) through a randomization stratification approach, according to a block randomization of 4.

The experimental group will receive 12 robot-assisted gait training sessions over 6 weeks (2 sessions/week). The control group will receive 12 conventional therapy sessions over 6 weeks (2 sessions/week), that will focus on gait training.

Primary outcome measures will be both neurophysiological measures (motor unit firing rate characteristics) and clinical test for gait speed (10m walking test). Secondary outcome measures will include: clinical tests of walking endurance (six minute walking test), balance (Berg Balance Test) and mobility (Up and Go Test).

Clinical assessment of lower-extremities spasticity (Modified Ashworth Scale), motor fatigue (Fatigue Severity Scale), depression (PHQ-9) and quality of life (SF-36) will be monitored. Subject acceptance and confidence in the treatments will be track with a Visual Analog Scale. Outcome measures will be assessed the week prior to treatment initiation (T0), after 6 sessions (T1), the week after the end of treatment (T2) and at 3 months follow-up (T3) to evaluate treatments retention, by a clinician blinded to the treatment.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physical Medicine and Rehabilitation Department

Ferrara, 44100, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • males and females, community dwelling, age 18 or older
  • diagnosis of multiple sclerosis in a stable phase, with relapses > 6 months prior to study enrollment
  • moderate to severe gait impairments referred to Expanded Disability Status Scale (EDSS) between 6 and 7

Exclusion criteria

  • neurologic conditions in addition to multiple sclerosis that may affect motor function
  • medical conditions likely to interfere with the ability to safely complete the study
  • impaired cognitive functioning: Mini Mental Status Examination < 24
  • severe lower-extremities spasticity or contractures that may limit range of motion(Ashworth score >4 for hip, knee or ankle flexors/extensors

Treatment and study plan

Lokomat (Hocoma, Switzerland)

Behavioral

Other names: robotic-driven gait orthosis

Conventional Therapy

Behavioral

Primary outcomes

  1. motor unit firing rate characteristics

    Time frame: 12 months

    It will be performed through the analysis of superficial EMG signals during isometric knee extension.

Secondary outcomes

  1. walking endurance

    Time frame: 12 months

    six minute walking test

  2. mobility

    Time frame: 12 months

    Timed Up and Go Test

  3. balance

    Time frame: 12 months

    Berg Balance Test

  4. gait speed

    Time frame: 12 months

    10 meter test

  5. Fatigue

    Time frame: 12 months

    Fatigue Severy Scale

  6. quality of life

    Time frame: 12 months

    SF-36

  7. depression

    Time frame: 12 months

    patient health questionnaire (PHQ-9)

Sponsors and collaborators

Lead sponsor

University Hospital of Ferrara

Other

Collaborators

  • Azienda Ospedaliero, Universitaria Pisana

Registry information

Official study title

The Effects of Robot-assisted Gait Training on Locomotor Function and Motor Unit Firing in Multiple Sclerosis Subjects With Severe Gait Impairments. A Randomized Control Trial

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Sep 19, 2011
Registry last updated
Jan 16, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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