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Clinical Trials/CTRI/2025/10/095891
CTRI/2025/10/095891
Not yet recruiting
Not Applicable

Efficacy of Pelvic Proprioceptive Neuromuscular Facilitation (PNF) on Trunk Balance and Gait in Individuals with Traumatic Incomplete Paraplegia

Lovely Professional University1 site in 1 country12 target enrollmentStarted: October 22, 2025Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
12
Locations
1
Primary Endpoint
For Trunk Balance— BBS (Berg Balance Scale), TUG (Timed Up and Go Test), mFRT (modified Functional Reach Test).

Overview

Brief Summary

Spinal Cord Injury refers to damage to spinal cord tissue, which causes deprivation of motor functions and sensory responses, along with dysfunction of the autonomic nervous system in the area below the damaged location. Neurological function preservation determines whether an SCI injury falls under the complete or incomplete categories. Progressive spinal cord injuries damage only some neural pathways to keep the lower part of the body active. This condition is known as incomplete SCI. This study focused on subjects with spinal cord injuries below the T6 neurological level since these patients preserve upper body movements, which enables concentrated trunk and leg therapy. Patients with T6 neurological severity and below maintain upper body movement control; therefore, they can better engage with pelvic P-PNF therapy to enhance trunk stability along with walking abilities. The effectiveness of pelvic PNF techniques has been observed in stroke and CP patients, but not enough research has been conducted regarding its application in SCI rehabilitation for incomplete paraplegics below T6. This investigation includes aims to determine the potential advantages of P-PNF techniques in evaluating their benefits in this population. Participants will be randomly assigned to either the Experimental group (pelvic PNF) or the Control group (conventional physiotherapy) on the base of evalution.  These group will teste by the outcome measures before starting the procedure (pre-intervention) and the end of the last visit of patients (post-intervention). The total time period of the procedusre is three days a week for four weeks. This investigation aims to determine the potential advantages of P-PNF techniques in evaluating their benefits in this population.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
20.00 Year(s) to 40.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Diagnosed with incomplete paraplegia due to SCI (Spinal Cord Injury) below the T6 (level of injury).
  • Patient walk with assistive device (e.g.sticks).
  • No other neurological conditions
  • Medically stable without complication.

Exclusion Criteria

  • Age below 20 years and above 40 years Injuries above T6 level
  • Non-ambulatory or complete dependent individuals
  • History of stroke, cerebral palsy, or muscular dystrophy
  • Presence of underlying conditions like cardiac disease, OA (osteoarthritis), and pressure ulcers.

Outcomes

Primary Outcomes

For Trunk Balance— BBS (Berg Balance Scale), TUG (Timed Up and Go Test), mFRT (modified Functional Reach Test).

Time Frame: Pre-intervention (before starting the procedure) and post-intervention (after 4 weeks of completion the procedure)

For Gait-FGA (Functional Gait Assessment), 3-MWT (3-Meter Walk Test)

Time Frame: Pre-intervention (before starting the procedure) and post-intervention (after 4 weeks of completion the procedure)

Gait variables: stride length, cadence, and walking speed.

Time Frame: Pre-intervention (before starting the procedure) and post-intervention (after 4 weeks of completion the procedure)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other [LPU, School of Allied Medical Science ]
Responsible Party
Principal Investigator
Principal Investigator

Komal

Lovely Professional University

Study Sites (1)

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