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Effect of Electrical Stimulation with Video Game based training for Sitting Balance in Individuals with Incomplete Spinal Cord Injury

Effectiveness of Sensory Electrical Stimulation Augmented Virtual Reality Training in Improving Sitting Balance and Quality of Life in Individuals with Incomplete Spinal Cord Injury - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065897
Enrollment
22
Registered
2024-04-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: S24- Injury of nerves and spinal cord at thorax level

Interventions

Intervention1: Sensory Electrical Stimulation (SES) Augmented Virtual Reality (VR) Training: Individuals in the intervention group will receive sensory electrical stimulation in the form of Transcutan

Sponsors

Indian Spinal Injuries Centre - Institute of Rehabilitation Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of SCI 2. T6- T12 Level of injury 3. ASIA B,C and D 4. Ability to sit unsupported for 10 seconds 5. Minimum of 90 degree shoulder flexion

Exclusion criteria

Exclusion criteria: 1. Uncorrected hearing or visual impairment 2. Deformity of upper limb, any other psychiatric, neurological or musculoskeletal impairment 3. History of severe recent urinary tract infection or autonomic dysreflexia 4. Refusal or inability to provide informed consent and inability to follow commands 5. Subjects with any contraindications for electrical stimulation such as pressure sores (grade 2 or more) at the site of stimulation and cardiac pacekmaker.

Design outcomes

Primary

MeasureTime frame
Sitting Balance (Forward reach distance) using Modified Functional Reach TestTimepoint: 0 weeks (Baseline, Pre-test) and 4 weeks (Post-test)

Secondary

MeasureTime frame
Multidirectional reach distance using Star Test (Using Tecnobody Prokin 252)Timepoint: 0 weeks (Baseline, Pre-test) and 4 weeks (Post-test);Quality of Life Using International Spinal Cord Society (ISCoS) QoL Basic Data Set Version 1.0Timepoint: 0 weeks (Baseline, Pre-test) and 4 weeks (Post-test)

Countries

India

Contacts

Public ContactNikhil Chowdhary

Indian Spinal Injuries Centre - Institute of Rehabilitation Sciences

shef0604@gmail.com9891770151

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 17, 2026