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Validation of the final version of a patient questionnaire to identify treatment-relevant upper limb spasticity movement disorder after stroke

Validation of the final version of a patient questionnaire to identify treatment-relevant upper limb spasticity movement disorder after stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035505
Enrollment
150
Registered
2025-02-07
Start date
2024-10-15
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

spastic movement disorder

Interventions

Group 1: All patients receive a questionnaire to assess the severity of the three cardinal symptoms of a spastic movement disorder (stiffness of the affected joints, restriction of movement control, l

Sponsors

KABEG-Gailtal-Klinik Hermagor
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Part 1 Patients with a first infarction of the middle cerebral artery (acute, subacute or chronic) or a Hemorrhage in the basal ganglia Preserved capacity for insight and judgement Adequate understanding of language and tasks, Attention span for 15 minutes Part 2 Additionally patients with cerebral or spinal cord injury (stroke, traumatic brain injury) or another chronic disease of the central nervous system (amyotrophic lateral sclerosis ALS, hereditary spastic spinal paralysis HSP, Parkinson's, MS, Alzheimer's) in their medical history.

Exclusion criteria

Exclusion criteria: Patients with other neurological diseases Reduced vigilance or attention span Patients with adult representation Patients with severe speech impairment

Design outcomes

Primary

MeasureTime frame
1. Correlation of patients' self-assessment of stiffness with the categories of the modified Ashworth Scale (mAS) 2. Correlation of patients' self-assessment of movement control with the categories of the MRC (Medical Research Counsil Scale, MRS). 3. Correlation of patients' self-assessment of pain/discomfort with the categories of the SAAPS. The collected data will be analyzed with regard to correlation between the patients‘ estimation and the examiners results.

Secondary

MeasureTime frame
Descriptive statistics of demographic data and duration since stroke. Descriptive statistics of the three clinical parameters to check whether all severity categories (muscle tone, movement control, pain) are represented. Descriptive statistics of the self-assessment questionnaire with regard to the representation of the severity categories.

Countries

Austria, Germany

Contacts

Public ContactKlemens Fheodoroff

KABEG-Gailtal-Klinik Hermagor

studien.gailtal-klinik@kabeg.at04282222071441

Outcome results

None listed

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