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Inter-rater Reliability of the Australian Spasticity Assessment Scale (ASAS) in Post-stroke Spasticity

I

Izmir Katip Celebi University

Status

Completed

Conditions

Hemiplegia, Spastic

Treatments

Other: Australian Spasticity Assessment Scale

Study type

Observational

Funder types

Other

Identifiers

NCT04613661
2020-GOKAE-0450

Details and patient eligibility

About

The reliability of the Australian Spasticity Assessment Scale (ASAS) has been reported to be not high enough in adult patients with acquired brain damage. The low number of patients and the heterogeneous study population have been reported as important limitations in the reliability study of this measure. Therefore, the reliability of the ASAS needs to be confirmed in stroke patients with spasticity. This study aims to investigate the inter-rater reliability of the ASAS in a study population consisting of a larger and more homogeneous patient population (those with post-stroke spasticity).

Full description

Spasticity is a motor disorder characterized by a velocity-dependent increase in tonic stretch reflex due to upper motor neuron lesion. The prevalence of post-stroke spasticity is between 17-40%. In the assessment of spasticity, although biomechanical and neurophysiological methods provide quantitative data, semi-quantitative methods are mostly used clinically. The most frequently used spasticity measures are the Modified Ashworth Scale and the Modified Tardieu Scale. However, these methods have significant disadvantages. Therefore, the search for more reliable clinical measures continues. One of the newly developed clinical scales is called the Australian Spasticity Assessment Scale (ASAS). Although ASAS has been reported to have a high level of reliability in children with cerebral palsy, the same has not been detected in adult patients with acquired brain damage. The low number of patients and the heterogeneous study population have been reported as two of the important limitations in the reliability study of this measure.

In this study, researchers aim to investigate the inter-rater reliability of the ASAS in a study population consisting of a larger and more homogeneous patient population (those with post-stroke spasticity).

Enrollment

85 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Chronic stroke (> 6 months)
  • Fist stroke
  • Increased tone according to the Modified Ashworth Scale in at least one of the elbow, wrist, and ankle
  • Stability of spasticity for the last 3 months

Exclusion criteria

  • Increased tone due to causes other than stroke (traumatic brain injury, spinal cord injury, multiple sclerosis, motor neuron disease, etc.)
  • Acute or subacute stroke (≤6 months)
  • Recurrent stroke attacks
  • Presence of contracture and/or moderate to severe pain in the joints to be assessed (elbow, wrist, and ankle)
  • Botulinum toxin injection in the last three months
  • History of neurolysis for spasticity (alcohol or phenol)
  • History of surgery for spasticity
  • Initiation of a new drug for spasticity, or a change in drug dose

Trial design

85 participants in 2 patient groups

Researcher 1
Description:
The first researcher assessing elbow, wrist, and ankle spasticity, respectively
Treatment:
Other: Australian Spasticity Assessment Scale
Researcher 2
Description:
The second researcher assessing elbow, wrist, and ankle spasticity, respectively
Treatment:
Other: Australian Spasticity Assessment Scale

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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