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Feasibility of inertial sensor-based real-time gait feedback therapy in individuals after stroke, with spinal cord injury and age-related gait disorders

Feasibility of inertial sensor-based real-time gait feedback therapy in individuals after stroke, with spinal cord injury and age-related gait disorders - RehaGait

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00011853
Enrollment
45
Registered
2017-03-23
Start date
2015-07-20
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

sensorimotor incomplete spinal cord injury stroke unphysiological gait pattern due to old age (geriatric patients) I69.4

Interventions

Group 1: 5x 2-3 min feedback training per visit. Three training visits take place on 3 consecutive days. The feedback system consisting of 2 shoe-mounted inertial sensors and 1 tablet PC calculates r

Sponsors

Klinik für Paraplegiologie - Experimentelle Neurorehabilitation
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with spinal cord injury: age = 18 years; motor incomplete (ASIA Impairment Scale (AIS) C, D); time after injury > 6 weeks; minimum walking ability: 20 min, WISCI II = 10; leg braces: maximal ankle support; 6 Min-Test = 100 m. Patients after stroke: age = 18 years; Mini-Mental-Status-Test (MMST) score = 18 ; time after paralysis > 3 months; minimum walking ability: 20 min; leg braces: maximal ankle support; 6 Min-Test = 100 m. Geriatric patients: age = 65 years; minimum walking ability: 20 min.

Exclusion criteria

Exclusion criteria: Patients with spinal cord injury and patients with stroke: difference in leg length > 3 cm; extreme spasticity, MAS (unilaterally) = 10; epileptic seizures; severe cognitive impairment. Geriatric patients: severe dementia; persisting stroke symptoms; insecure usage of walking aids (walker, walking stick).

Design outcomes

Primary

MeasureTime frame
Change in mean training level (1 level = 1 SD of the physiological norm of the chosen training parameter) at initial gait analysis of visits 1 through 3.

Secondary

MeasureTime frame
Improvement in gait speed in the 10-Meter-Walk-Test on even ground without FB before and after the training phase of the study.

Countries

Germany

Contacts

Public ContactDaniel Schließmann

Experimentelle Neurorehabilitation, Klinik für Paraplegiologie, Universitätsklinikum Heidelberg

daniel.schliessmann@med.uni-heidelberg.de062215629152

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 6, 2026