Effect of Sensorimotor Training on Pain and Gait Performance in Patients With Discogenic Sciatica

This study aims to investigate the effect of sensorimotor training on gait performance in patients with discogenic sciatica.

Study Overview

• Status: Not yet recruiting
• Conditions: Sciatica Due to Intervertebral Disc Disorder
• Intervention / Treatment: Other: Standard physical therapy; Other: Sensorimotor Training

Detailed Description

Discogenic sciatica is commonly associated with pain, functional limitations, and alterations in gait performance resulting from nerve root involvement and impaired neuromuscular control. Sensorimotor training is an active rehabilitation approach that integrates sensory input with motor responses and may improve proprioception, postural control, balance, and movement coordination.

This study will investigate the additional effect of sensorimotor training in patients with chronic discogenic sciatica. Participants will receive a conventional physical therapy program consisting of interferential current therapy, hot packs, positioning according to directional preference, and static abdominal and back exercises. The experimental intervention will incorporate additional sensorimotor training, including proprioceptive neuromuscular facilitation (PNF)-based trunk exercises, balance training on unstable surfaces, colored-path sensorimotor exercises, and the Star Excursion Balance Exercise.

The sensorimotor program will use progressive task-specific exercises designed to challenge proprioception, balance, trunk control, and neuromuscular coordination. Exercise difficulty will be gradually progressed according to participants' abilities through changes in surface stability, movement complexity, reach distance, walking speed, and the incorporation of dual-task activities.

The study will evaluate changes in spatiotemporal gait parameters, pressure-pain threshold, and functional disability before and after the intervention. The findings may provide evidence regarding whether adding sensorimotor training to conventional physical therapy offers additional benefits for gait performance, pain-related outcomes, and functional ability in patients with chronic discogenic sciatica.

• Study Type: Interventional
• Enrollment (Estimated): 30
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Yara Ahmed Mansour, B.Sc; Phone Number: +20 10 08350127; Email: yara.a.mansour@deltauniv.edu.eg
• Study Contact Backup: Name: Hend Mohammad Elsayed Ismail, PhD

Study Locations

• Egypt
  • Gamasa, Egypt
    • Outpatient clinic at the Faculty of Physical Therapy, Delta University
    • Contact: Yara Ahmed Mansour, B.Sc; Phone Number: +20 10 08350127; Email: yara.a.mansour@deltauniv.edu.eg

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Thirty patients of both sexes diagnosed with lumbar disc herniation affecting the L4-L5 and/or L5-S1 nerve roots will be included in this study.
• Presence of lumbar disc herniation (LDH) will be confirmed by magnetic resonance imaging (MRI).
• Age will range from 30 to 55 years.
• Patients experiencing radiating pain along the sciatic nerve distribution (symptoms persisting for more than 3 months).
• All patients must be employed in office-based jobs.
• Berg Balance Scale score will range from 21 to 40 (moderate balance impairment).
• Body Mass Index (BMI) will be within the normal to overweight range (18.5 29.9 kg/m²).
• All the patients will be able to walk independently with or without minimal assistance.

Exclusion Criteria:

• Patients with a history of spinal surgery will be excluded.
• Presence of central neurological disorders (e.g., stroke).
• Patients with other causes of low back pain which is not related to discogenic origin.
• Affections of the musculoskeletal system including fractures.
• Patients with severe balance impairment (Berg Balance Scale score < 21).
• Presence of vestibular disorders or visual impairments affecting balance.
• Patients are currently participating in other rehabilitation programs.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Standard physical therapy; Participants in this arm will receive a standard physical therapy program consisting of interferential current therapy, hot packs, positioning according to directional preference, and static abdominal and back exercises. The treatment will be administered three sessions per week for two months, with each session lasting approximately 45-60 minutes.	Other: Standard physical therapy; Standard physical therapy will include interferential current therapy applied over the lumbar region at 80-100 Hz for 15-20 minutes, hot packs applied over the lumbar paraspinal region for 10 minutes, positioning according to the patient's directional preference for 10 minutes or as tolerated, and static abdominal and back exercises targeting the transversus abdominis and multifidus. The exercises will be performed as 3 sets of 10 repetitions, with each contraction held for 10 seconds followed by 5 seconds of rest.
Experimental: Sensorimotor Training Plus Standard Physical Therapy; Participants in this arm will receive the same standard physical therapy program administered to the active comparator arm, in addition to a sensorimotor training program. The sensorimotor training will include PNF-based trunk exercises, balance training on unstable surfaces, colored-path sensorimotor exercises, and the Star Excursion Balance Exercise. The treatment will be administered three sessions per week for two months, with each session lasting approximately 45-60 minutes.	Other: Standard physical therapy; Standard physical therapy will include interferential current therapy applied over the lumbar region at 80-100 Hz for 15-20 minutes, hot packs applied over the lumbar paraspinal region for 10 minutes, positioning according to the patient's directional preference for 10 minutes or as tolerated, and static abdominal and back exercises targeting the transversus abdominis and multifidus. The exercises will be performed as 3 sets of 10 repetitions, with each contraction held for 10 seconds followed by 5 seconds of rest.; Other: Sensorimotor Training; Sensorimotor training will include PNF-based trunk exercises, balance training on unstable surfaces, colored-path sensorimotor exercises, and the Star Excursion Balance Exercise. The program will incorporate progressive challenges to trunk control, balance, proprioception, and neuromuscular coordination. Progression will include unstable surfaces, alternating limb movements, single-leg and cross bridging, increased walking speed, dual-task activities, increased reach distance, and increased exercise complexity according to patient tolerance.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Walking Speed	Walking speed will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported in meters per second (m/s).	2 months
Stride Length	Stride length will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported in millimeters (mm).	2 months
Cadence	Cadence will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported as steps per minute (steps/min).	2 months
Stance Time	Stance time will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported in seconds (s).	2 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pressure-Pain Threshold	Pressure-pain threshold will be assessed using a pressure algometer at the lumbar paraspinal, gluteus medius, and piriformis muscles. Higher values indicate greater pressure-pain tolerance.	2 months
Functional Disability	Functional disability will be assessed using the Oswestry Disability Index (ODI). The score will be expressed as a percentage from 0% to 100%, with higher scores indicating greater disability.	2 months

Collaborators and Investigators

• Sponsor: Cairo University
• Investigators: Study Chair: Moshera Hassan Darwiesh, PhD, Professor, Cairo University; Study Director: Omar Mohamed Said, PhD, Lecturer, Cairo University; Study Director: Hend Mohammad Elsayed Ismail, PhD, Lecturer, Delta University

Study record dates

Study Major Dates

• Study Start (Estimated): September 7, 2026
• Primary Completion (Estimated): January 7, 2027
• Study Completion (Estimated): January 21, 2027

Study Registration Dates

• First Submitted: September 1, 2026
• First Submitted That Met QC Criteria: September 1, 2026
• First Posted (Actual): September 4, 2026

Study Record Updates

• Last Update Posted (Actual): September 4, 2026
• Last Update Submitted That Met QC Criteria: September 1, 2026
• Last Verified: September 1, 2026

More Information

Terms related to this study

• Other Study ID Numbers: F.PT. 2607107

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No