Multimodal PT With and Without Proprioceptive Training in Lumber FJS

Riphah International University

Status: Enrolling

Conditions: Facet Joint Pain

Treatments: Other: Multimodal Physical therapy; Other: Proprioceptive training along with and Multimodal Physical therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT05931653

REC/RCR&AHS/23/1102

Details and patient eligibility

About

This will be a randomized clinical trial. The study will be conducted at Pakistan Railways General Hospital Rawalpindi and Riphah International Hospital Islamabad. Patients with FJS will be included. The aim of this study is to find the comparative effects of multimodal physical therapy treatment and proprioceptive training along with multimodal physical therapy treatment on pain, lumbar ranges of motion, disability, fatigue, lumbar lordosis curvature and balance.

Participants will be assessed for pain, lumbar range of motions, lumbar lordosis, disability, fatigue and balance before treatment. The intervention duration is 06 weeks, 03 sessions per week will be given to all participants. Pain and lumbar ranges of motion will be measured on every visit. At the end of 06th week final readings for functional status, fatigue level, lumbar lordosis angle, fall risk and limits of stability will also be recorded. Data will be analyzed by SPSS v.23.

Enrollment: 50 estimated patients

Sex: All

Ages: 25 to 53 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with facet joint syndrome diagnosed by standard criteria. This criterion includes:

  • One point tenderness under X-ray radiography
  • Kemp sign.
  • Catching pain.
  • Pain increases with lumbar extension.
  • Pain with bilateral SLR.
  • Or pain diminishes with Medial branch block or Facet joint block.
  • Provocation Maneuver. Acevedo sign (Facet stress sign) Unilateral facet palpation Percussion spinal test Impaired range of motion Jump test
  • Revel's criteria 05 out of 07- 1. age greater than 65 years and pain that was not exacerbated by coughing, not worsened by hyperextension, not worsened by forward flexion, not worsened when rising from flexion, not worsened by extension-rotation, and well-relieved by recumbency.

Standing flexion, returning from standing flexion, standing extension, the extension rotation test.

• On Biodex balance system (BBS), overall stability index between 0.7-2.8.
• On Biodex balance system (BBS) Limits of stability Anterior: less than 80, posterior: less than 40 and lateral: less than 160 (80 on each side) 75% LOS (moderate level).
• NPRS ratings greater than 4
• Constant or Intermittent pain worsening on repeated movements

Exclusion criteria

• T-score of -2.5 or lower.
• BMI is 30.0 or higher.
• Patients with Lumbar Postural Syndrome
• Patients with Lumbar Instability
• Post laminectomy/discectomy
• Spondylolisthesis
• Osteoporosis/Fractures
• Cauda equine syndrome
• Recent history of spinal trauma or surgery
• Lumbar myelopathy
• Patients with known metabolic diseases
• Participants having less than 20% ODI scoring

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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50 participants in 2 patient groups

Multimodal Physical Therapy

Experimental group

Description:

Multimodal Physical therapy/Traditional Physical therapy

Treatment:

Other: Multimodal Physical therapy

Proprioceptive training along with Multimodal Physical Therapy

Experimental group

Description:

Proprioceptive training along with Multimodal Physical Therapy

Treatment:

Other: Proprioceptive training along with and Multimodal Physical therapy