Skip to content

A comparative study on the validity and sensitivity of TSS and MAS in assessing post-stroke spasticity

A comparative study on the validity and sensitivity of TSS and MAS in assessing post-stroke spasticity

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018427
Enrollment
Unknown
Registered
2018-09-18
Start date
2018-10-08
Completion date
Unknown
Last updated
2018-09-24

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

Conditions

Spasticity

Interventions

Gold Standard:Modified Ashworth Scale
Tardieu&#32

Sponsors

Department of Rehabilitation Medicine, Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Voluntary participation, the patient himself understands and signs or the legal guardian signs the informed consent form; (2) Conform to the diagnosis of "stroke" in "Diagnostic Points of Various Cerebrovascular Diseases" adopted by the Fourth National Conference on Cerebrovascular Diseases in 1995, and showed a single infarction or hemorrhage on the side by CT or MRI. kitchen; (3) The MAS score of the hemiplegia was >1, and the muscle tension of the healthy limb was normal; (4) The first occurrence of stroke or previous lacunar infarction without sequelae; (5) The onset time is =1 month; (6) Aged 18 to 80 years old, male or female; (7) The condition is stable, the consciousness is clear, and the vital signs are stable.

Exclusion criteria

Exclusion criteria: (1) Patients who have Parkinson's disease and other high muscle tone; (2) Patients who have serious cognitive, verbal, visual, hearing or mental disorders and other effects of examination and treatment; (3) Patients who had a lacunar infarction and have sequelae; (4) Patients who have tumors, severe respiratory, heart, liver, kidney, endocrine and hematopoietic systems; (5) Patients who have joint with disease (such as joint surgery or rheumatoid arthritis); (6) There are contraindications for surface electromyography or ultrasound (such as epidermal damage, fever, etc.) (7) Participating in other clinical trials who influence the evaluation of the results of this study

Design outcomes

Primary

MeasureTime frame
spasticity;SEN;

Countries

China

Contacts

Public ContactWenting Qin

Department of Rehabilitation Medicine, Huashan Hospital, Fudan University

475161275@qq.com+86 13761765515

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026