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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01145105
Other study ID # K-09-0078-ctil
Secondary ID
Status Completed
Phase N/A
First received May 24, 2010
Last updated November 9, 2011
Start date June 2010
Est. completion date July 2011

Study information

Verified date July 2011
Source Clalit Health Services
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Low back pain ( LBP) is a significant health problem which affects about 70%-80% of the population during the course of their life . The majority of LBP is resolved within 3 months; however, up to 40% of LBP becomes chronic. One subgroup of chronic LBP is patients with sciatica. Sciatica is characterized by radiating pain to the buttock and lower limb, with or without low back pain.

It has been shown in the upper limb that by positioning the contra-lateral arm in tension the investigators actually reduce tension in the ipsilateral arm. Patients, who present with symptoms like sciatica, can benefit from this maneuver (neural dynamics techniques) that reduces tension through the contra-lateral leg.

Working Hypothesis: Compared with a placebo maneuver of the upper limb, the neural dynamics techniques will result in better rehabilitation of individuals with radicular LBP.


Description:

Objectives: To evaluate the efficacy of neural dynamics techniques, using the contra-lateral leg, in the treatment of sub-acute/chronic Low back pain with radiation to the leg. Study Methodology: Eligible individuals will be assessed by a physiotherapist that will be blinded to the treatment allocation; treatment (either intervention or placebo) will be provided by a physiotherapist that will be blinded to the patient's assessment. The treated individuals and the referring physician will also be blinded to the treatment allocation;


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date July 2011
Est. primary completion date July 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Written consent

- LBP with radiation to one leg, that lasts more than 6 weeks

- Abnormal response to SLR test

- With or without neurological signs

Exclusion Criteria:

- History of spinal surgery

- Patient with FUO

- History of malignancies

- Patient with saddle anesthesia

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
neural dynamics techniques treatment
Treatment group- will receive neural mobilizations techniques, to improve movement of the sciatic nerve.
placebo treatment
Control group- will receive placebo treatment that will include mobilization to the upper limb. After the placebo treatment, these patients will receive neural mobilizations techniques.

Locations

Country Name City State
Israel Clalit Health Services, Haifa and Western Galilee District Haifa

Sponsors (1)

Lead Sponsor Collaborator
Clalit Health Services

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy of neural dynamics technique Efficacy will be measured by combining 5 tools
Oswestry disability index.
McGill Pain Questionnaire
Visual analog scale for pain assessment.
Lumbar flexion measurement (the distance of the tip of the index finger to the inferior angle of the Patella, measured by a measurement tape.
Passive SLR range of motion- measured with inclinometer
5 weeks No
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