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Exploring the impact of Tyromotion Balance machine on patients with spinal injury with and without current

Effects of Tyromotion Balance Board with Epidural stimulation on Postural Control in individuals with Spinal Cord Injury: A Clinical Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064055
Enrollment
40
Registered
2024-03-13
Start date
Unknown
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

Health Condition 1: M991- Subluxation complex (vertebral) Health Condition 2: S220- Fracture of thoracic vertebra

Interventions

Intervention1: Tymo Balance Therapy: The plates for Tymo therapy Tymo system Tyromotion Austria a wirelesss static and dynamic platform, for evaluating and rehabilitating posture In the study group. T

Sponsors

Galgotias University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Incomplete SCI graded as AIS B C and D Level of lesion: T10 and above based on AIS level determination by the PI with preservation of conus function The intact distance between the cone and the lesion must be at least 60mm Focal spinal cord disorder caused by either trauma or epidural subdural or intramedullary bleeding Minimum 12 months post-injury Completed in-patient rehabilitation program Able to stand with walker or 2 crutches Stable medical and physical condition as considered by Investigators Adequate caregiver support and access to appropriate medical care in patients home community Agree to comply in good faith with all conditions of the study and to attend all required study training and visits Must participate in two training sessions before enrolment Must provide and sign Informed Consent prior to any study related procedures

Exclusion criteria

Exclusion criteria: Limitation of walking function based on accompanying (CNS) disorders (systemic malignant disorders, cardiovascular disorders restricting physical training, peripheral nerve disorders) History of significant autonomic dysreflexia Cognitive/brain damage Epilepsy Patient who uses an intrathecal Baclofen pump. Patient who has any active implanted cardiac device such as pacemaker or defibrillator. Patient who has any indication that would require diathermy. Patient who has any indication that would require MRI. Patient that have an increased risk for defibrillation

Design outcomes

Primary

MeasureTime frame
Using Tyromotion board Displacement Cop Sway area Weight distribution Duration of standing Duration of sitting balance. Age (yr) Sex-Male/Female SCIâ??injury level AIS MOTOR SCORE SENSORY SCORE vmc HIP FLEXORS Knee extensors Dorsiflexors FIST SCORE Timepoint: Baseline,4th week and 8th week

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactSurbhi Kaura

Galgotias University

physiosurbhi123@gmail.com8527389589

Outcome results

None listed

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