Reliability of Spasticity Measurement With Lokomat

Status

Suspended

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02718053

Enrollment

Registered

2016-03-24

Start date

2015-07-31

Completion date

Unknown

Last updated

2016-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spasticity, Lokomat

Brief summary

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

Interventions

OTHERL-stiff

spasticity measurement with Lokomat

OTHERAshworth

spasticity measurement with Ashworth scale

Study design

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Yes

Inclusion criteria

* patients affected by lower limbs spasticity

Exclusion criteria

* medical contraindications to mobilization with Lokomat

Design outcomes

Primary

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

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026