Reliability of Spasticity Measurement With Lokomat

Spasticity, Lokomat Clinical Trial

Clinical Trial Details — Status: Suspended

Administrative data

• NCT number: NCT02718053
• Other study ID #: spasticity01
• Status: Suspended
• Phase: N/A
• First received: March 11, 2016
• Last updated: September 29, 2016
• Start date: July 2015

Study information

• Verified date: September 2016
• Source: Ospedale Generale Di Zona Moriggia-Pelascini
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: Ethics Committee
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Suspended
• Enrollment: 20
• Est. primary completion date: May 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• patients affected by lower limbs spasticity

Exclusion Criteria:

• medical contraindications to mobilization with Lokomat

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

• Muscle Spasticity
• Spasticity, Lokomat

Intervention

Other:
• L-stiff
spasticity measurement with Lokomat
• Ashworth
spasticity measurement with Ashworth scale

Locations

Country	Name	City	State
Italy	Ospedale Generale di Zona Moriggia Pelascini	Gravedona ed Uniti	CO

Sponsors (1)

Lead Sponsor	Collaborator
Ospedale Generale Di Zona Moriggia-Pelascini

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	correlation of spasticity measurement obtained with L-Stiff (Lokomat) and Ashworth scale		1 day	No