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A STUDY TO COMPARE THE EFFECTIVENESS OF TRUNK TRAINING EXERCISE IN CONJUNCTION WITH MUCSLE STIMULATOR VERSUS TRUNK TRAINING EXERCISE ALONE ON TRUNK BALANCE IN INDIVIDUAL WITH SPINAL CORD INJURY

EFFECTIVENESS OF GOAL ORIENTED TASK SPECIFIC TRAINING IN CONJUNCTION WITH NMES ON TRUNK BALANCE IN INDIVIDUALS WITH SPINAL CORD INJURY

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032598
Enrollment
20
Registered
2021-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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: NMES GOAL ORIENTED TASK SPECIFIC TRAINING: NMES GOAL ORIENTED TASK SPECIFIC TRAINING Intervention2: 1)NMES 2)GOAL ORIENTED TASK SPECIFIC TRANING: NMES( 4 ELECTRODES,2 over thoracic e

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patient with SCI( traumatic/ non traumatic) 2)Participants with Age 18ââ?¬â??60 years 3)Atleast 3 months prior to the study 4)ASIA grade B ,C and D SCI who are receiving physical and occupational therapy. 5)Ã? C5 or below neurological level. 6)Able to sit unsupported for at least 10ââ?¬â?°seconds. 7)90 degree or more shoulder flexion.

Exclusion criteria

Exclusion criteria: 1)Progressive non traumatic SCI. 2)Participants with cognitive impairment (inability to understand Instructions, Mini Mental State Examination score ⩽ 24. 3)Orthopedic problems influencing unsupported sitting or Deformity of Upper extremity. 4)Pressure ulcers on the buttocks ,grade 3 & 4 or had pressure areas necessitating bed rest. 5)Cardiopulmonary insufficiency, cardiac pacemaker, Oncological disease, epilepsy, open wounds, or metal implants in the area where electrical stimulator is plan to be perform.

Design outcomes

Primary

MeasureTime frame
1)Modified Functional Reach Test 2) Function In Sitting Test(FIST) Timepoint: (0 day - 3 weeks)

Secondary

MeasureTime frame
1)SCIM III VersionTimepoint: (0 days - 3 weeks)

Countries

India

Contacts

Public ContactShefali walia

ISIC Institute of Rehabilitation Sciences

shef0604@gmail.com9891770151

Outcome results

None listed

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