Reliability of Spasticity Measurement With Lokomat

September 29, 2016 updated by: Ilaria Zivi, Ospedale Generale Di Zona Moriggia-Pelascini
The purpose of the study is to evaluate the reliability of spasticity measurement with Lokomat

Study Overview

Status

Suspended

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Italy
    • CO
      • Gravedona ed Uniti, CO, Italy, 22015
        • Ospedale Generale di Zona Moriggia Pelascini

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

subjects are selected from patients hospitalized in our neurorehabilitation unit

Description

Inclusion Criteria:

  • patients affected by lower limbs spasticity

Exclusion Criteria:

  • medical contraindications to mobilization with Lokomat

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
controls
healthy subjects
Other: L-stiff
spasticity measurement with Lokomat
Other: Ashworth
spasticity measurement with Ashworth scale
spasticity
patients affected by spasticity of the lower limbs
Other: L-stiff
spasticity measurement with Lokomat
Other: Ashworth
spasticity measurement with Ashworth scale

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
correlation of spasticity measurement obtained with L-Stiff (Lokomat) and Ashworth scale
Time Frame: 1 day
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Ospedale Generale Di Zona Moriggia-Pelascini

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2015

Primary Completion (ACTUAL)

May 1, 2016

Study Registration Dates

First Submitted

March 11, 2016

First Submitted That Met QC Criteria

March 19, 2016

First Posted (ESTIMATE)

March 24, 2016

Study Record Updates

Last Update Posted (ESTIMATE)

September 30, 2016

Last Update Submitted That Met QC Criteria

September 29, 2016

Last Verified

September 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • spasticity01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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