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Efficacy of Proprioceptive Neuromuscular Facilitation and Task Specific Training on Trunk control and Wheelchair Propulsion in Spinal Cord Injury Patients

Effect of Integrated Motor Control Training Program on Sitting Balance, Wheelchair Propulsion and Functional Status in patients with Incomplete Spinal Cord Injury - A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109883
Enrollment
44
Registered
2026-04-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: G958- Other specified diseases of spinalcord Health Condition 2: S242- Injury of nerve root of thoracic spine Health Condition 3: S342- Injury of nerve root of lumbar andsacral spine

Interventions

Intervention1: Integrated Motor Control Training Program (Trunk Proprioceptive Neuromuscular Facilitation Technique along with Task Specific Training): Trunk Proprioceptive Neuromuscular Facilitation

Sponsors

Pravara Institute of Medical Sciences (Deemed to be University)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Incomplete spinal cord injury 2.Both traumatic and non-traumatic patients 3.Neurological level below T4 4.FIST score 24-30 5.Both male and female patients 6.Age between 20 to 60 years

Exclusion criteria

Exclusion criteria: 1.Patient with acute injuries 2.Patients with Complete SCI (ASIA A) 3.Patients with cognitive impairment 4.Presence of psychiatric and neurological dysfunction 5.Any recent musculoskeletal disorders of upper and lower extremities 6.Patients with diagnosed medical red flags 7.Patients unwilling to participate. 8.Patient with contractures, unhealed fractures, pressure sores, severe spasticity

Design outcomes

Primary

MeasureTime frame
1.Function in Sitting Test (FIST-SCI) (ICC=0.95) 2.Timed Manual Wheelchair Slalom Test (MWST) (ICC=0.98)Timepoint: Pre intervention i.e 0 week, Post intervention i.e. after 6 weeks and Follow up will be taken after 1 month

Secondary

MeasureTime frame
Spinal Cord Independence Measure-III (SCIM-III) (ICC=0.94)Timepoint: Pre intervention i.e 0 week, Post intervention i.e. after 6 weeks and Follow up will be taken after 1 month

Countries

India

Contacts

Public ContactDr Mohit Kumar Chatterjee

Dr. APJ Abdul Kalam College of Physiotherapy, PIMS(DU)

pnb2609@gmail.com9168572881

Outcome results

None listed

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