Gait analysis in acute and chronic SCI patients before and after training with wearable cyborg HAL - Hybrid Assistive Limb

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00020805

Enrollment

Registered

2020-02-12

Start date

2018-04-23

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Acute and chronic SCI G82 S14 S24 S34

Interventions

Group 1: Pre test - 60 training sessions - post test

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with a gait disorder due to an acute ( 1 year) spinal cord lesion.

Exclusion criteria

Exclusion criteria: Cardiopulmonary comorbidities, pressure ulcers on the lower extremity / breech region, infections, osteoporosis, thromboses / embolisms in the past, contractures or higher-grade spasticity of the lower extremity, body weight > 100 kg. Epilepsy, the presence of electronic medical devices that cannot be removed (e.g. pacemakers).

Design outcomes

Primary

Measure	Time frame
At the beginning and at the end of the individual training period (60 sessions, approx. 3 months), a gait analysis is carried out using inertial sensors to record the individual gait change.	—

Secondary

Measure	Time frame
Functional test procedures (10-meter walk test, 6-minute walk test, timed up-and-go test, WISCI-II score) are evaluated secondarily.	—

Countries

Germany

Contacts

Public ContactAlexis Brinkemper

Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil GmbH

alexis.brinkemper@bergmannsheil.de02343026918

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 14, 2026