To Compare Effect Of Virtual Reality and t-DCS on Sitting Balance, Function and Quality of Life in Incomplete spine cord injury Patient

Comparative Effectiveness of Virtual reality and t-DCS on sitting balance control, function and quality of life in individual with incomplete spinal cord injury - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/03/105799

Enrollment

Registered

2026-03-10

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: G959- Disease of spinal cord, unspecified

Interventions

Intervention1: t-DCS: ROM EXERCISES FOR UL AND LL 2 SETS ,12 REPITITION MAT EXERCISES-ROLLING,KNEELING,LONG SITTING 2 REPS ,5 MIN HOLD PROGRESSION-TIMING OF HOLD WILL BE INCREASED DEPENDING ON PATIENT

Eligibility

Inclusion criteria

Inclusion criteria: 1.Person diagnosed with incomplete spinal cord injury 2.Chronic SCI- 1 year of injury 3.MMSE Score-min 24 out of 30 4.People with age 18-45 5.Both gender 6.ASIA scores C and D 7.Level of injury T6-T12 8.Individual should sit unassisted for at least 1 min and have minimum of 90 degree shoulder flexion

Exclusion criteria

Exclusion criteria: 1.Participants having any condition interfering with regime like metal implant at site of stimulation 2.Un-corrected Visual defect 3.Deformity of upper extremity 4.H/O Neuromuscular disorder or autonomic dysreflexia 5.H/O Conditions like cardio respiratory,Neurological and muscular disorder 6..Un cooperative individual 7.Lack of consent

Design outcomes

Primary

Measure	Time frame
1.Modified functional Reach test (mFRT) Timepoint: pre intervention at day o and post intervention at week 4	—

Secondary

Measure	Time frame
Function in sitting test assessment twice during an interval of 4 weeksTimepoint: pre intervention at day 0 & post intervention at week 4;scim iii assessment twice during an interval of 4 weeksTimepoint: pre intervention at day 0 & post intervention at week 4;.International spinal cord injury Quality of life basic data set Data assessment twice during an interval of 4 weeks Form (version 2.0)Timepoint: pre intervention at day 0 & post intervention at week 4	—

Measure

Time frame

Function in sitting test assessment twice during an interval of 4 weeksTimepoint: pre intervention at day 0 & post intervention at week 4;scim iii assessment twice during an interval of 4 weeksTimepoint: pre intervention at day 0 & post intervention at week 4;.International spinal cord injury Quality of life basic data set Data assessment twice during an interval of 4 weeks Form (version 2.0)Timepoint: pre intervention at day 0 & post intervention at week 4

—

Countries

India

Contacts

Public ContactDr Bharti Sharma

Gurugram University

bhartisharma@gurugramuniversity.ac.in8700188196

Outcome results

None listed

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