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Effectiveness of a Novel Neural Tissue Management to Improve Short-term Pain and Disability in Patients With Sciatica

Effectiveness of a Novel Neural Tissue Management to Improve Short-term Pain and Disability in Patients With Sciatica

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03663842
Enrollment
44
Registered
2018-09-10
Start date
2010-05-10
Completion date
2010-12-10
Last updated
2018-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Disability Evaluation, Manual Therapies, Physical Therapy Modalities, Sciatica Pain

Keywords

Lumbosacral Plexus, Physical Therapy Modalities, Manual Therapies, Disability Evaluation.

Brief summary

Objectives: To analyse the effects of sciatic neural mobilisation, in combination to the treatment of the surrounding structures, on pain and disability. Secondly, to investigate baseline characteristics that may be associated with improvements in pain and lumbar disability. Methods: Twenty-eight patients with a clinical diagnosis of sciatica were treated with neural mobilization, joint mobilisation and soft tissue techniques. Pain intensity and lumbar disability were assessed at baseline and after treatment using a Numerical Rating Scale (0-10) and the Oswestry Disability Index (0-100), respectively. The pre- and post-intervention data were compared.

Interventions

All patients underwent the same techniques, and there was no modification of the intervention protocol during the study: (1) Myofascial release technique - piriformis muscle and biceps femoral muscle; (2) Hip joint mobilization; (3) Cross-fiber friction over the sacroiliac joints; (4) Neural mobilization to improve sciatic nerve excursion.

Sponsors

Centro Universitário Augusto Motta
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Low back pain with radiating leg pain and/or paresthesia below the knee that follows the L5 and/or S1 dermatomal pattern.

Exclusion criteria

* History of lumbar and abdominal surgery * Rheumatologic syndromes (e.g. Rheumatoid arthritis); * Lumbar stenosis.

Design outcomes

Primary

MeasureTime frameDescription
Pain intensityFrom enrollment to end of treatment at 12 weeksMeasured by the Numerical Rating Scale (NRS 0-10)
Lumbar disabilityFrom enrollment to end of treatment at 12 weeks.Assessed by the Oswestry Disability Index (ODI).It consists of 10 items addressing different aspects of disability. Each item is scored from 0 to 5, with higher values representing greater disability. The sum of the item scores is divided by the total possible score (50 if all sections are completed), and the resulting total is multiplied by 100 to be described as a percentage score.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026