Skip to content

Balance training in Incomplete Spinal cord Injury patients

Efficacy of Electrical stimulation augmented virtual reality training in improving balance in Incomplete Spinal Cord Injury patients: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/12/016814
Enrollment
48
Registered
2018-12-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: S199- Unspecified injury of neck

Interventions

Intervention1: Electrical Stimulation-Augmented Virtual reality based balance training: Subjects in Group 1 shall receive Electrical stimulation while performing balance exercises on Nintendo Wii. Sti
penguin slide
tightrope and table tilt, with six minutes of practice for each game

Sponsors

Indian Spinal Injuries Centre Institute of rehabilitation Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: SCI categorized as American Spinal Injury Association (ASIA) C or D more than 6 months after ISCI Level of injury- from C5 to L1. Age 18-45 years. Able to stand with or without the support of an assistive device for a minimum of 2 minutes. Willing to participate in the study. Mini Mental Status Examination scores, MMSE >24

Exclusion criteria

Exclusion criteria: Subjects having Spinal shock Subjects with any other neurological problem, any musculoskeletal condition or psychiatric problem which will interfere with the treatment. Pain scored greater than 5 on an 11-point numerical rating pain scale (0, no pain; 10, most severe pain). Any other recent complication that can interfere with participation. Symptoms of Orthostatic Hypotension upon standing. Subjects with severe depression (Beck Depression Inventory -II (>=29). Subjects with spasticity of grade 3 or more on Modified Ashworth Scale. subjects with any contraindications for Electrical Stimulation, such as Cardiac Pacemakers, Skin lesions or rash at potential sites, Grade 4 pressure ulcers anywhere on the lower extremities, Grade 2 or 3 pressure ulcers at locations where ES is to be applied.

Design outcomes

Primary

MeasureTime frame
Muscle strength Balance Functional Mobility Timepoint: 0 weeks, 4 weeks and 8 weeks

Secondary

MeasureTime frame
Quality of lifeTimepoint: 0 weeks, 4 weeks and 8 weeks

Countries

India

Contacts

Public ContactDr Pragya Kumar

Amity Institute of Physiotherapy

pkumar24@amity.edu9878529787

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 11, 2026