Reliability of Spasticity Measurement With Lokomat

NCT ID: NCT02718053

Last Updated: 2016-09-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

SUSPENDED

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-07-31

Brief Summary

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The purpose of the study is to evaluate the reliability of spasticity measurement with Lokomat

Detailed Description

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Conditions

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Spasticity, Lokomat

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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spasticity

patients affected by spasticity of the lower limbs

L-stiff

Intervention Type OTHER

spasticity measurement with Lokomat

Ashworth

Intervention Type OTHER

spasticity measurement with Ashworth scale

controls

healthy subjects

L-stiff

Intervention Type OTHER

spasticity measurement with Lokomat

Ashworth

Intervention Type OTHER

spasticity measurement with Ashworth scale

Interventions

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L-stiff

spasticity measurement with Lokomat

Intervention Type OTHER

Ashworth

spasticity measurement with Ashworth scale

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patients affected by lower limbs spasticity

Exclusion Criteria

* medical contraindications to mobilization with Lokomat
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ospedale Generale Di Zona Moriggia-Pelascini

OTHER

Sponsor Role lead

Responsible Party

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Ilaria Zivi

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ospedale Generale di Zona Moriggia Pelascini

Gravedona Ed Uniti, CO, Italy

Site Status

Countries

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Italy

Other Identifiers

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spasticity01

Identifier Type: -

Identifier Source: org_study_id