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The Findings of Ultrasound Elastography and ARFI in Strokes Patients With Spastic Elbow Flexor

The Correlation Between Clinical Examination and Ultrasound Elastography Acoustic Radiation Force Impulse Findings in Hemiplegic Patients With Elbow Flexor Spasticity After Stroke

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02557711
Enrollment
50
Registered
2015-09-23
Start date
2016-06-30
Completion date
2017-09-30
Last updated
2016-03-30

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

Conditions

Cerebrovascular Accident

Keywords

spasticity, stroke, ultrasound elastography, acoustic radiation force impulse

Brief summary

The aim of this study: 1. To evaluate the correlation between the clinic tools and ultrasound elastography/ ARFI imaging in stroke patients. 2. To assess the reliability of elastography/ ARFI imaging in spasticity evaluation of stroke patients.

Detailed description

Modified Ashworth Scale (MAS) and Modified Tardieu Scale (MTS) are the most commonly used tools for spasticity assessment. But these clinic methods cannot reveal the architecture and stiffness of muscles. In recent years, ultrasound elastography and acoustic radiation force impulse (ARFI) are used in musculoskeletal disorders, including spasticity. There are no studies about the correlation between spasticity and ultrasound elastography /ARFI imaging in stroke patients. The investigators will enroll 50 stroke patients with hemiplegia and biceps brachii muscle spasticity. One physical therapist will measure MAS and MTS for spasticity of biceps brachii muscle. Two physiatrists will perform ultrasound elastography and ARFI for intra-rater and inter-rater reliability evaluation. The evaluations of B-mode ultrasound, elastography and ARFI included Heckmatt scale, biceps brachii ratio, strain ratio, dynamic sonoelastography score, color intensity, and shear wave velocity. After performing all assessments, the investigators will analyze the correlation between the clinic tools and elastography/ ARFI imaging and evaluate the reliability of elastography/ ARFI imaging in spasticity evaluation.

Interventions

DEVICEultrasound elastography, acoustic radiation force impulse

Two physiatrists will perform ultrasound elastography and ARFI for intra-rater and inter-rater reliability evaluation.

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* stroke patients with hemiplegia and biceps brachii muscle spasticity.

Exclusion criteria

* elbow joint contracture deformity * combined other neuromuscular system disease * affected upper extremity has local infection * patient who can't follow instruction, who is restlessness and whose elbow can't meet the positioning criteria

Design outcomes

Primary

MeasureTime frame
Modified Ashworth Scale (MAS), Modified Tardieu Scale (MTS)patients will be evaluated within 1 month after basic history taking and consent signing

Secondary

MeasureTime frame
the thickness of biceps brachiipatients will be evaluated within 1 month after basic history taking and signing consent
Heckmatt scalepatients will be evaluated within 1 month after finishing history taking and consent signing
strain ratiopatients will be evaluated within 1 month after finishing history taking and consent signing
Dynamic Sonoelastography Score(DS score)patients will be evaluated within 1 month after finishing history taking and consent signing
The mean values of the intensity of red, green, and blue on histogram of bicep brachiipatients will be evaluated within 1 month after finishing history taking and consent signing
shear wave velocity within region of interest between biceps brachii and brachialispatients will be evaluated within 1 month after finishing history taking and consent signing

Countries

Taiwan

Contacts

Primary ContactPong Ya-Ping, MD
yaping0707@gmail.com889-7-7317123

Outcome results

None listed

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