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Reliability of Spasticity Measurement With Lokomat

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02718053
Recruitment Status : Suspended
First Posted : March 24, 2016
Last Update Posted : September 30, 2016
Sponsor:
Information provided by (Responsible Party):
Ilaria Zivi, Ospedale Generale Di Zona Moriggia-Pelascini

Study Description
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Brief Summary:
The purpose of the study is to evaluate the reliability of spasticity measurement with Lokomat

Condition or disease Intervention/treatment
Spasticity, Lokomat Other: L-stiff Other: Ashworth

Study Design
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Study Type : Observational
Estimated Enrollment : 20 participants
Time Perspective: Prospective
Study Start Date : July 2015
Actual Primary Completion Date : May 2016
Groups and Cohorts
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Group/Cohort Intervention/treatment
spasticity
patients affected by spasticity of the lower limbs
 Other: L-stiff
spasticity measurement with Lokomat

Other: Ashworth
spasticity measurement with Ashworth scale
controls
healthy subjects
 Other: L-stiff
spasticity measurement with Lokomat

Other: Ashworth
spasticity measurement with Ashworth scale


Outcome Measures
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Primary Outcome Measures :
  1. correlation of spasticity measurement obtained with L-Stiff (Lokomat) and Ashworth scale [ Time Frame: 1 day ]

Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
subjects are selected from patients hospitalized in our neurorehabilitation unit
Criteria

Inclusion Criteria:

  • patients affected by lower limbs spasticity

Exclusion Criteria:

  • medical contraindications to mobilization with Lokomat
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02718053


Locations
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Italy
Ospedale Generale di Zona Moriggia Pelascini
Gravedona ed Uniti, CO, Italy, 22015
Sponsors and Collaborators
Ospedale Generale Di Zona Moriggia-Pelascini
More Information
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Responsible Party: Ilaria Zivi, MD, Ospedale Generale Di Zona Moriggia-Pelascini
ClinicalTrials.gov Identifier: NCT02718053    
Other Study ID Numbers: spasticity01
First Posted: March 24, 2016    Key Record Dates
Last Update Posted: September 30, 2016
Last Verified: September 2016
Additional relevant MeSH terms:
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Muscle Spasticity
Muscular Diseases
Musculoskeletal Diseases
Muscle Hypertonia
 Neuromuscular Manifestations
Neurologic Manifestations
Nervous System Diseases