ClinicalTrials.Veeva

Menu

Validity and Reliability of the 12-item Multiple Sclerosis Walking Scale (12-WS) in Subjects With Spinal Cord Injury (12-WS SCI)

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

Spinal Cord Injuries
Gait Disorders, Neurologic

Treatments

Other: 12 MSWS questionnaire

Study type

Interventional

Funder types

Other
NETWORK

Identifiers

NCT06256159
2023-02304

Details and patient eligibility

About

Established gait assessments for subjects with spinal cord injury (SCI) (6MWT, 10MWT, TUG, SCIM III and WISCI II) are widely used in the clinical and research setting. So far, no valid measurement exists that assesses the patients' perspective of walking ability in SCI. As there is the 12-item Multiple Sclerosis Walking Scale (12-WS) to assess the patients' perspective on gait ability in patients with multiple sclerosis, it is hypothesized that the 12-WS would also be a valid instrument for subjects with incomplete SCI. The main goal of this study is to collect data from clinical gait assessments in subjects with spinal lesions and to demonstrate that the 12-WS is a valid and reliable patient-reported outcome measurement for individuals with incomplete spinal cord injury.

Enrollment

67 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-80 years
  • Diagnosis of chronic spinal cord injury (>6 months; cervical or thoracic motor incomplete traumatic or non-traumatic (AIS C, D) above T12
  • Must have impaired walking function as demonstrated by neurological examination.

Exclusion criteria

  • Women who are pregnant or breast feeding
  • Current orthopaedic problems of lower limbs
  • History of major cardiac condition (e.g., infarction, insufficiency (NYHA II-IV))
  • History of major pulmonary condition (e.g., chronic obstructive pulmonary disease GOLD II-IV
  • Current major depression or psychosis
  • Participation in another interventional study (except specTra-study) that may have an impact on walking function.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Sequential Assignment

Masking

None (Open label)

67 participants in 1 patient group

Patients with incomplete spinal cord injury
Other group
Treatment:
Other: 12 MSWS questionnaire

Trial contacts and locations

2

Loading...

Central trial contact

Sibylle Achermann, SC; Sabrina Imhof, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems