Skip to content

Treadmill training under transcutaneous spinal cord stimulation - a randomized controlled trial in patients with spastic gait disorder in neurological rehabilitation

Treadmill training under transcutaneous spinal cord stimulation - a randomized controlled trial in patients with spastic gait disorder in neurological rehabilitation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00036450
Enrollment
20
Registered
2025-03-24
Start date
2025-04-07
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Spastic gait disorder as a partial symptom of spastic movement disorder caused by central nervous system damage (e.g. stroke, multiple sclerosis or spinal cord lesions) G35-G37 I60-I69 S14 S24 S34 G80.1 G80.2 G82

Interventions

Group 1: Patients with spastic gait disorder who receive a combined treatment of transcutaneous spinal cord stimulation and treadmill training (5 units within 15 days). Group 2: Patients with spastic

Sponsors

Deutsche Sporthochschule Köln, Institut für Bewegungstherapie und bewegungsorientierte Prävention und Rehabilitation, Abteilung Bewegungsorientierte Präventions- und Rehabilitationswissenschaften
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: IG and KG: presence of a spastic gait disorder (e.g. due to a stroke, spinal cord injury or other neurological disease); Functional Ambulation Categories (FAC) > 0 (ability to walk present); cognitive ability to participate in the study present; stable medical condition.

Exclusion criteria

Exclusion criteria: IG and KG: FAC = 0 (no walking ability); electrical implants (e.g. pacemaker; unstable cardiopulmonary status; florid infections, decubitus dermatological diseases or malignant diseases in the stimulation area; diagnosed seizures (e.g. epilepsy); pregnancy.

Design outcomes

Primary

MeasureTime frame
The walking ability of all study participants is measured using standardized tests (10MWT; TUG; 2mWT) at the start of the study (baseline) and after the end of the 15th rehabilitation day.

Secondary

MeasureTime frame
The health-related quality of life (EQ-5D) and the perceived fear of falling (FES-I) of all study participants are measured at the start of the study (baseline) and after the end of the 15th rehabilitation day.

Countries

Germany

Contacts

Public ContactJonas Gorges

Deutsche Sporthochschule Köln, Institut für Bewegungstherapie und bewegungsorientierte Prävention und Rehabilitation, Abteilung Bewegungsorientierte Präventions- und Rehabilitationswissenschaften

j.gorges@dshs-koeln.de+49 15110090557

Outcome results

None listed

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