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Low Back PainNCT04022798

Management of LBP With Radiculopathy.

A study testing Exercise, manual therapy in people with Low Back Pain, run by University of Tabuk at 1 site in Saudi Arabia.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Low Back Pain
What is being tested?
Exercise, manual therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteSaudi Arabia
Study dates
1 Jul 2019to 30 Nov 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Salem F Alatawi, PhD contact

0549638301

sfalatawi@ut.edu.sa

Saudi Arabia1 site, 1 recruiting
  • Salem F Alatawi

    Tabuk, 71491

    Salem F Alatawi, Phd, 549638301, sfalatawi@ut.edu.sa

    Ahmad S Almasoudi, PhD, 00966503579505, aelmasoudy@ut.edu.sa

    Recruiting

Other trials in Saudi Arabia

About this study

Official title: Randomized Controlled Trial of Effectiveness of Neural Mobilization in the Management of Chronic Low Back Pain With Radiculopathy.

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).

Read the 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:
  2. 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.
  3. 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.
  4. Publication of the study, local and international. Work Flow
  5. 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.
  6. Co-investigator will be assigned as custodian to all data and investigations from the start of the study.
  7. Co-investigator will be assigned to record all financial transaction according to the policies of sponsoring unit of the university.
  8. Co-investigator will be responsible logistic and making sure all researched needed are adequate and available when needed.
  9. A clear communication and coordination scheme will be established.
  10. 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.
Conditions
Low Back Pain
Being tested
Exercise, manual therapy
Keywords
Low back pain, Neural mobilization, lumbar stabilization exercise, Radial extracorporeal shock wave therapy
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Exercise, manual therapyOther

    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.

Study groups in NCT04022798
Study groupRoleWhat they receive
Experimental groupExperimentalNeural mobilization (NM), lumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT)
Receives: Other: Exercise, manual therapy
Control groupActive comparatorlumbar stabilization exercise (LSE) and Radial Extracorporeal Shock Wave Therapy (rESWT)
Receives: Other: Exercise, manual therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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).

    Measured: baseline, 3 weeks and 6 weeks

  2. 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).

    Measured: baseline, 3 weeks and 6 weeks

  3. 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).

    Measured: baseline, 3 weeks and 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Jul 2019
  2. Study start1 Jul 2019
  3. Primary completion30 Oct 2019 (estimated)
  4. Study completion30 Nov 2019 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Experimental group: Group A (NM, LSE and rESWT) and Control group: Group B (LSE and rESWT).
Masking
Single blind
Who is masked
Participant
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04022798
Sponsor's protocol ID
UTabuk
Status last verified
Jul 2019
First submitted
8 Jul 2019
Last updated
17 Jul 2019
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: After publication

Questions about this trial

What is this clinical trial studying?

A study testing Exercise, manual therapy in people with Low Back Pain, run by University of Tabuk at 1 site in Saudi Arabia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 17 Jul 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Salem F Alatawi, PhD (0549638301, sfalatawi@ut.edu.sa), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Pain is being assessed using NPRS (time frame: baseline, 3 weeks and 6 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jul 2019.

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