Effect of Sensorimotor Training on Pain and Gait Performance in Patients With Discogenic Sciatica
1 other identifier
interventional
30
1 country
1
Brief Summary
This study aims to investigate the effect of sensorimotor training on gait performance in patients with discogenic sciatica.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 1, 2026
CompletedFirst Posted
Study publicly available on registry
September 4, 2026
CompletedStudy Start
First participant enrolled
September 7, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 7, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 21, 2027
September 4, 2026
September 1, 2026
4 months
September 1, 2026
September 1, 2026
Conditions
Outcome Measures
Primary Outcomes (4)
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 Outcomes (2)
Pressure-Pain Threshold
2 months
Functional Disability
2 months
Study Arms (2)
Standard physical therapy
ACTIVE COMPARATORParticipants 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.
Sensorimotor Training Plus Standard Physical Therapy
EXPERIMENTALParticipants 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.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Outpatient clinic at the Faculty of Physical Therapy, Delta University
Gamasa, Egypt
Study Officials
- 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
Central Study Contacts
Hend Mohammad Elsayed Ismail, PhD
CONTACT
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
September 1, 2026
First Posted
September 4, 2026
Study Start
September 7, 2026
Primary Completion (Estimated)
January 7, 2027
Study Completion (Estimated)
January 21, 2027
Last Updated
September 4, 2026
Record last verified: 2026-09