NCT07805265

Brief Summary

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

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
4mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress20%
Sep 2026Jan 2027

First Submitted

Initial submission to the registry

September 1, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 4, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

September 7, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 7, 2027

Expected
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 21, 2027

Last Updated

September 4, 2026

Status Verified

September 1, 2026

Enrollment Period

4 months

First QC Date

September 1, 2026

Last Update Submit

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 COMPARATOR

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

Sensorimotor Training Plus Standard Physical Therapy

EXPERIMENTAL

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 therapyOther: Sensorimotor Training

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.

Sensorimotor Training Plus 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.

Sensorimotor Training Plus Standard Physical TherapyStandard physical therapy

Eligibility Criteria

Age30 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Study Sites (1)

Outpatient clinic at the Faculty of Physical Therapy, Delta University

Gamasa, Egypt

Location

Study Officials

  • Moshera Hassan Darwiesh, PhD

    Professor, Cairo University

    STUDY CHAIR
  • Omar Mohamed Said, PhD

    Lecturer, Cairo University

    STUDY DIRECTOR
  • Hend Mohammad Elsayed Ismail, PhD

    Lecturer, Delta University

    STUDY DIRECTOR

Central Study Contacts

Yara Ahmed Mansour, B.Sc

CONTACT

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

Locations