Measuring the impact of spasticity after spinal cord Injury on quality of life. Not Applicable
Conditions
Interventions
After obtaining informed consent, the pre-final version of the PRISM questionnaire in German is presented to the patients for completion and a semi-structured interview is conducted to assess the comp
Sponsors
Universität für Weiterbildung Krems
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients with clinically confirmed spinal cord injury of traumatic, nontraumatic, or congenital origin. 2. Patients from 3 months after the spinal cord lesion onwards. 3. Patients with existing spasticity symptoms 4. Age = 18 years 5. Good knowledge of written and spoken German 6. Signed voluntary informed consent for study participation
Exclusion criteria
Exclusion criteria: Decreased cognitive and language abilities
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Qualitative semi-structured interviews to test the comprehensibility of the translated version of the "Patient reported impact of spasticity measure" for measuring the impact of spasticity after spinal cord injury on quality of life. Qualitative analysis of the interviews: Content analysis according to Mayring | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
Austria
Contacts
Public ContactAnja Largler
Outcome results
None listed