Reliability of Spasticity Measurement With Lokomat

Suspended

• Conditions: Spasticity, Lokomat
• Interventions: Other: L-stiff; Other: Ashworth

• Registration Number: NCT02718053
• Lead Sponsor: Ospedale Generale Di Zona Moriggia-Pelascini

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2015-07
• Study First Submitted: 2016-03-11
• Study First Submitted QC: 2016-03-19
• Study First Posted: 2016-03-24
• Primary Completion: 2016-05
• Status Verified: 2016-09
• Last Update Submitted: 2016-09-29
• Last Update Posted: 2016-09-30

Recruitment & Eligibility

• Status: SUSPENDED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• patients affected by lower limbs spasticity

Exclusion Criteria

• medical contraindications to mobilization with Lokomat

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
controls	L-stiff	healthy subjects
controls	Ashworth	healthy subjects
spasticity	Ashworth	patients affected by spasticity of the lower limbs
spasticity	L-stiff	patients affected by spasticity of the lower limbs

Primary Outcome Measures

Name	Time	Method
correlation of spasticity measurement obtained with L-Stiff (Lokomat) and Ashworth scale	1 day

Trial Locations

Locations (1)

Ospedale Generale di Zona Moriggia Pelascini; 🇮🇹 Gravedona ed Uniti, CO, Italy