Management of LBP With Radiculopathy.
Primary Purpose
Low Back Pain
Status
Unknown status
Phase
Not Applicable
Locations
Saudi Arabia
Study Type
Interventional
Intervention
Exercise, manual therapy
Sponsored by
About this trial
This is an interventional treatment trial for Low Back Pain focused on measuring Low back pain, Neural mobilization, lumbar stabilization exercise, Radial extracorporeal shock wave therapy
Eligibility Criteria
Inclusion Criteria:
- Lower back pain should be Lower than 5 on the Visual Analogue Scale,
- > 18 years,
- Not taken physical therapy treatment in the past 6 months period,
- No previous surgery, such as structural anomalies, spinal cord compressions, severe instabilities, severe osteoporosis, acute infections, severe cardiovascular or metabolic diseases,
- A body mass index less than 30kg/m2.
Exclusion Criteria:
- Pain with a score above 5 on the Visual Analogue Scale (VAS),
- ≤ 18 years,
- Had physical therapy treatment in the past 6 months period,
- Had undergone previous surgery, such as structural anomalies, spinal cord compressions, severe instabilities, severe osteoporosis, acute infections, severe cardiovascular or metabolic diseases,
- pregnant
- A body mass index above 30kg/m2.
Sites / Locations
- Salem F AlatawiRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Experimental group
Control group
Arm Description
Neural mobilization (NM), lumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT)
lumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT)
Outcomes
Primary Outcome Measures
Change in Pain is being assessed using NPRS
Pain was assessed by using NPRS, where 0 represented no pain and 10 represented the worst pain possible, to indicate the intensity of pain in the lower back (Jensen et al., 1994).
Change in Disability is being assessed using the Modified Oswestry Disability Questionnaire
Disability was measured by using the Modified Oswestry Disability Questionnaire (MODQ) which is a self-rating questionnaire used to evaluate functional physical disability (Rajfur, et al., 2017).
Change in Lumbar flexion range of motion is being assessed using modified Schober method
Lumbar flexion range of motion was measured by using modified Schober method (Philadelphia Panel Members, 2001).
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04022798
Brief Title
Management of LBP With Radiculopathy.
Official Title
Randomized Controlled Trial of Effectiveness of Neural Mobilization in the Management of Chronic Low Back Pain With Radiculopathy.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
October 30, 2019 (Anticipated)
Study Completion Date
November 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Tabuk
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is to determine the effectiveness of Neural mobilization(NM) technique compared with lumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT) in the physical therapy management of chronic low back pain (CLBP) with radiculopathy. Subjects will be randomly assigned into two groups. Group A (NM, LSE and rESWT) and Group B (LSE and rESWT).
Detailed Description
Randomized clinical control trail will be conducted in the North West area of Saudi Arabia.
Patients diagnosed to have CLBP with radiculopathy at three different hospitals in Saudi Arabia will be recruited for this study.
Participants will be randomly assigned into treatment or control group. Before starting of the study, the author will designe the treatment and control group treatment program and instructed the treating physiotherapists in their implementation. An ethical approval was approved by the ethics committee of the University of Tabuk- Saudi Arabia. Participants in each group will receive 12 treatment sessions of 45 minutes each, 2 days a week for 6 consecutive weeks.
For each group, a menu of a lumbar stabilization program was designed. This program included 8 levels of exercise ( single leg knee to chest stretch, double leg knee to chest, supine piriformis stretch, supine hamstring stretch, lower trunk rotation stretch, lumbar rotation stretch, pelvic tilt, pelivic tilt with alternative legs). Exercises were tailored for each individual ability and, if possible, progressed at each session which would last approximately 30 minutes. Each single exercise was repeated many times based on the patient's clinical condition. All sessions were provided by physiotherapists. After finishing of session of lumbar stabilization program, a shock wave therapy was applied for each participant in a prone position over the region of low back pain (Figure 2 ).
Only participants in the treatment group were receive neural mobilization technique. This includes the following: sciatic neural mobilization technique (Figure 3), slump neural mobilization technique (Figure 4) and self neural mobilization (Figure 5 ).
OUTCOME MEASUREMENT TOOLS:
There were three outcome measures as following: pain, disability and lumbar spine range of motion. Subjected were tested three times as following: at the baseline (0 week), at the mid of treatment (3 weeks) and finally at the end of treatment (6 weeks).
Pain Pain was assessed by using NPRS, where 0 represented no pain and 10 represented the worst pain possible, to indicate the intensity of pain in the lower back (Jensen et al., 1994). Disability Disability was measured by using the Modified Oswestry Disability Questionnaire (MODQ) which is a self-rating questionnaire used to evaluate functional physical disability (Rajfur, et al., 2017).
Lumbar flexion range of motion Lumbar flexion range of motion was measured by using modified Schober method (Philadelphia Panel Members, 2001).
DATA ANALYSIS:
A simple descriptive statistical analysis was adopted to describe the patient specific demographic characteristics with respect to outcomes parameters. Within group and between groups comparison was analyzed using ANOVA and Scheffes' post-hoc tests by using SPSS 20.0.
Work Plan:
Roles and responsibilities :
1. Principal Investigator-is responsible for the following:
1. The management and integrity of the research design 2. Approval from ethical board committee or its equivalent 3. Preparation and conduct of the study 4. Reporting of the research project 5. Managing, monitoring and ensuring the integrity of any collaborative relationships.
6. Directs and oversees compliance, financial, personnel, and other related aspects and resources of the research project 7. Coordination with department and central administration personnel to assure research in is conducted in accordance with regulations of the University and sponsoring agency policies and procedures.
8. Publication of the study, local and international. Work Flow
The principal investigator will be responsible in check points, meetings, and coordination with the research team, regular meeting will be set on thursday every after two weeks and when necessary.
Co-investigator will be assigned as custodian to all data and investigations from the start of the study.
Co-investigator will be assigned to record all financial transaction according to the policies of sponsoring unit of the university.
Co-investigator will be responsible logistic and making sure all researched needed are adequate and available when needed.
A clear communication and coordination scheme will be established.
Co-investigator will be required to submit status accomplish report on regular basis determined by the team.
Utilization:
The outcomes of the research will be used to:
NM techniques enhance patient outcomes in the management of CLBP with radiculopathy when added to standard care.
NM technique applied by experienced physical therapists combined with LSE and ESWT in a brief clinical trial might better and earlier than LST and ESWT alone for decreasing pain, reducing back disability and improving function in patients with CLBP with radiculopathy symptoms.
The findings are interesting and motivate further studies, including long-term follow-up of large groups, randomized studies and the comparison of this treatment model with other treatment models.
A faster program with fewer hospital visits not only enables the patients to proceed with most of their daily activities but also decreases the costs of the treatment.
A NM technique might also be an alternative to conventional physiotherapy in the treatment of the CLBP patients with radiculopathy symptoms.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
Low back pain, Neural mobilization, lumbar stabilization exercise, Radial extracorporeal shock wave therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Experimental group: Group A (NM, LSE and rESWT) and Control group: Group B (LSE and rESWT).
Masking
Participant
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Neural mobilization (NM), lumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT)
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
lumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT)
Intervention Type
Other
Intervention Name(s)
Exercise, manual therapy
Intervention Description
Participants were randomly assigned into treatment (n=15) or control group (n=15). Participants in each group received 12 treatment sessions of 45 minutes each, 2 days a week for 6 consecutive weeks.
For each group, a menu of a lumbar stabilization program was designed. This program included 8 levels of exercise ( single leg knee to chest stretch, double leg knee to chest, supine piriformis stretch, supine hamstring stretch, lower trunk rotation stretch, lumbar rotation stretch, pelvic tilt, pelivic tilt with alternative legs). Exercises were tailored for each individual ability and, if possible, progressed at each session which would last approximately 30 minutes. Each single exercise was repeated many times based on the patient's clinical condition. All sessions were provided by physiotherapists.
Primary Outcome Measure Information:
Title
Change in Pain is being assessed using NPRS
Description
Pain was assessed by using NPRS, where 0 represented no pain and 10 represented the worst pain possible, to indicate the intensity of pain in the lower back (Jensen et al., 1994).
Time Frame
baseline, 3 weeks and 6 weeks
Title
Change in Disability is being assessed using the Modified Oswestry Disability Questionnaire
Description
Disability was measured by using the Modified Oswestry Disability Questionnaire (MODQ) which is a self-rating questionnaire used to evaluate functional physical disability (Rajfur, et al., 2017).
Time Frame
baseline, 3 weeks and 6 weeks
Title
Change in Lumbar flexion range of motion is being assessed using modified Schober method
Description
Lumbar flexion range of motion was measured by using modified Schober method (Philadelphia Panel Members, 2001).
Time Frame
baseline, 3 weeks and 6 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Lower back pain should be Lower than 5 on the Visual Analogue Scale,
> 18 years,
Not taken physical therapy treatment in the past 6 months period,
No previous surgery, such as structural anomalies, spinal cord compressions, severe instabilities, severe osteoporosis, acute infections, severe cardiovascular or metabolic diseases,
A body mass index less than 30kg/m2.
Exclusion Criteria:
Pain with a score above 5 on the Visual Analogue Scale (VAS),
≤ 18 years,
Had physical therapy treatment in the past 6 months period,
Had undergone previous surgery, such as structural anomalies, spinal cord compressions, severe instabilities, severe osteoporosis, acute infections, severe cardiovascular or metabolic diseases,
pregnant
A body mass index above 30kg/m2.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Salem F Alatawi, PhD
Phone
0549638301
Email
sfalatawi@ut.edu.sa
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Salem F Alatawi, PhD
Organizational Affiliation
University of Tabuk
Official's Role
Principal Investigator
Facility Information:
Facility Name
Salem F Alatawi
City
Tabuk
ZIP/Postal Code
71491
Country
Saudi Arabia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Salem F Alatawi, Phd
Phone
549638301
Email
sfalatawi@ut.edu.sa
First Name & Middle Initial & Last Name & Degree
Ahmad S Almasoudi, PhD
Phone
00966503579505
Email
aelmasoudy@ut.edu.sa
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
After publication
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