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Effect of Neural Mobilization on Lumbosacral Radiculopathy Patients With Peripheral Sensitization

Primary Purpose

Radiculopathy

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Neural mobilization exercises -Tensioner technique
Neural mobilization exercises -Slider technique
Transcutaneous Electrical Nerve Stimulation (TENS)
Sponsored by
Mohammed Al-Ghamdi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Radiculopathy focused on measuring Lumbosacral radiculopathy, peripheral sensitization, Neural mobilization, radicular LBP, slider, tensioner

Eligibility Criteria

18 Years - 60 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with lumbosacral radiculopathy with dominant peripheral sensitization
  • patients with unilateral leg pain.
  • patient S-LANSS score > 12,
  • negative sensory and motor examination.
  • positive neural tissue provocation tests (straight leg raising test, slump test).
  • adult.
  • pain duration of more than 3 months.

Exclusion Criteria:

  • S-LANSS score ≥ 12,
  • motor or sensory deficits,
  • history of back or lower extremity surgeries,
  • bilateral referred pain,
  • patients with pacemakers, cardiovascular problems, epilepsy, active malignancy, dermatological conditions, and diminished pain sensation.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Experimental

    Experimental

    Arm Label

    Control group

    Tensioner Group

    Slider Group

    Arm Description

    Patients in this group had 6 sessions in 2 weeks of Transcutaneous Electric Nerve Stimulation (TENS).

    Patients in this group had 6 sessions in 2 weeks of TENS combined with neural mobilization exercises (Tensioner technique).

    Patients in this group had 6 sessions in 2 weeks of TENS combined with neural mobilization exercises (Slider technique).

    Outcomes

    Primary Outcome Measures

    Visual Analog Scale
    Visual analog scale was used to measure pain intensity. This scale is a 10 cm line where patients chose from 0 to 10 (when 0 mean no pain and 10 mean maximum pain)
    Hip Flexion Range of Motion (Symptomatic Side)
    Change in Hip flexion range of motion during straight leg raising (symptomatic side)
    Knee Flexion Range of Motion (Symptomatic Side)
    Change in Knee flexion range of motion during slump (symptomatic side)
    Hip Flexion Range of Motion (Asymptomatic Side)
    Change in Hip Flexion Range of Motion During Straight Leg Raising (Asymptomatic Side)
    Knee Flexion Range of Motion (Asymptomatic Side)
    Change in Knee flexion range of motion during slump (Asymptomatic side)

    Secondary Outcome Measures

    Full Information

    First Posted
    July 30, 2018
    Last Updated
    February 28, 2023
    Sponsor
    Mohammed Al-Ghamdi
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03621878
    Brief Title
    Effect of Neural Mobilization on Lumbosacral Radiculopathy Patients With Peripheral Sensitization
    Official Title
    Effect of Neural Mobilization Techniques on Pain, and Hip and Knee Range of Motion on Lumbosacral Radiculopathy Patients With Peripheral Sensitization
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    July 1, 2015 (Actual)
    Primary Completion Date
    November 28, 2017 (Actual)
    Study Completion Date
    March 30, 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Mohammed Al-Ghamdi

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary purpose of this study was to investigate the effects of slider and tensioner techniques on pain, hip and knee ROM in lumbosacral radiculopathy patients with peripheral sensitization. A secondary purpose was to evaluate the correlation between these outcomes measurements.
    Detailed Description
    Study design: Double-blind case-control trial. Methods: Fifty-one male lumbosacral radiculopathy patients with peripheral sensitization, were divided into one of the three groups: slider, tensioner, and control. The primary outcome measurements were visual analog scale (VAS) for pain, hip range of motion (ROM) during SLR test, and knee flexion ROM during slump test. The measurements were taken at baseline, after 1st, 3rd, and 6th session. Statistical Analysis: A two-way mixed design analysis of variance (MANOVA) with post-hoc (Bonferonni Correction) was used to calculate the differences with Time (baseline, 1st,3rd,6th sessions) as a within-group factor and Group (control, slider, and tensioner) as a between-group factor. The effect size was calculated with Cohen's d. Pearson's correlation was used for correlation analysis.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Radiculopathy
    Keywords
    Lumbosacral radiculopathy, peripheral sensitization, Neural mobilization, radicular LBP, slider, tensioner

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Care ProviderOutcomes Assessor
    Masking Description
    both the examiner and the outcomes assessor where blinded to the participants groups. the primary investigator was also blind to the outcomes of each participant during the study period.
    Allocation
    Non-Randomized
    Enrollment
    51 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Control group
    Arm Type
    Active Comparator
    Arm Description
    Patients in this group had 6 sessions in 2 weeks of Transcutaneous Electric Nerve Stimulation (TENS).
    Arm Title
    Tensioner Group
    Arm Type
    Experimental
    Arm Description
    Patients in this group had 6 sessions in 2 weeks of TENS combined with neural mobilization exercises (Tensioner technique).
    Arm Title
    Slider Group
    Arm Type
    Experimental
    Arm Description
    Patients in this group had 6 sessions in 2 weeks of TENS combined with neural mobilization exercises (Slider technique).
    Intervention Type
    Other
    Intervention Name(s)
    Neural mobilization exercises -Tensioner technique
    Intervention Description
    Exercise aiming to lengthen the neural structure using more than one joint.
    Intervention Type
    Other
    Intervention Name(s)
    Neural mobilization exercises -Slider technique
    Intervention Description
    Exercise aiming to slide/glide the neural structure using more than one joint.
    Intervention Type
    Other
    Intervention Name(s)
    Transcutaneous Electrical Nerve Stimulation (TENS)
    Other Intervention Name(s)
    Control
    Intervention Description
    Electrotherapy device aiming to decrease patient's symptoms.
    Primary Outcome Measure Information:
    Title
    Visual Analog Scale
    Description
    Visual analog scale was used to measure pain intensity. This scale is a 10 cm line where patients chose from 0 to 10 (when 0 mean no pain and 10 mean maximum pain)
    Time Frame
    The measurements were taken at days "0,1,5,12"
    Title
    Hip Flexion Range of Motion (Symptomatic Side)
    Description
    Change in Hip flexion range of motion during straight leg raising (symptomatic side)
    Time Frame
    The measurements were taken at days "0,1,5,12"
    Title
    Knee Flexion Range of Motion (Symptomatic Side)
    Description
    Change in Knee flexion range of motion during slump (symptomatic side)
    Time Frame
    The measurements were taken at days "0,1,5,12"
    Title
    Hip Flexion Range of Motion (Asymptomatic Side)
    Description
    Change in Hip Flexion Range of Motion During Straight Leg Raising (Asymptomatic Side)
    Time Frame
    The measurements were taken at days "0,1,5,12"
    Title
    Knee Flexion Range of Motion (Asymptomatic Side)
    Description
    Change in Knee flexion range of motion during slump (Asymptomatic side)
    Time Frame
    The measurements were taken at days "0,1,5,12"

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with lumbosacral radiculopathy with dominant peripheral sensitization patients with unilateral leg pain. patient S-LANSS score > 12, negative sensory and motor examination. positive neural tissue provocation tests (straight leg raising test, slump test). adult. pain duration of more than 3 months. Exclusion Criteria: S-LANSS score ≥ 12, motor or sensory deficits, history of back or lower extremity surgeries, bilateral referred pain, patients with pacemakers, cardiovascular problems, epilepsy, active malignancy, dermatological conditions, and diminished pain sensation.

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    Effect of Neural Mobilization on Lumbosacral Radiculopathy Patients With Peripheral Sensitization

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