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
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
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
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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