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Instrumented spasticity assessment for use in clinical practice

Instrumented spasticity assessment for use in clinical practice - Instrumented spasticity assessment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON44548
Enrollment
15
Registered
2017-09-27
Start date
2017-08-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

spasticity

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Patients clinically diagnosed with spasticity (MAS > 0) - At least 18 years of age - Suffering from spasticity in either the elbow flexors or extensors, knee flexors or extensors, or ankle plantar flexors.

Exclusion criteria

Exclusion criteria: - Having undergone any surgical treatment that influences passive and/or active joint motion. - Presence of disturbing neurological signs like dystonia, rigidity and tremors. - Not able to read and/or understand the patient information letter.

Design outcomes

Primary

MeasureTime frame
Inter rater reliability of two instrumented spasticity scales (Modified Ashworth Scale, Modified Tardieu Scale).

Secondary

MeasureTime frame
Agreement between the instrumented and non-instrumented spasticity measurements. Algorithms to distinguish between neural and non-neural stiffness. Algorithms to evaluate other relevant clinical symptoms associated with spasticity.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)