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The Effect of Dry Needling of the Gluteus Medius Muscle in Patients With Chronic Low Back Pain

The Effect of Dry Needling in the Gluteus Medius Muscle With Active Physiotherapy Versus Placebo Dry Needling With Active Physiotherapy in Patients With Chronic Low Back Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04498572
Enrollment
25
Registered
2020-08-04
Start date
2020-10-01
Completion date
2022-07-15
Last updated
2024-04-22

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

Conditions

Low Back Pain

Brief summary

The effectiveness of dry needling of the Gluteus Medius muscle in combination with active exercises will be examined compared with sham needling with active exercises in low back pain (LBP) patients.

Detailed description

Objectives: To examine if dry needling in combination with active physiotherapy is more effective in reducing pain and increase activity of daily living, range of motion and muscle strength in patients with chronic low back pain compared to sham dry needling in combination with active physiotherapy. Methods: the study will include individuals with non-specific LBP over 3 months. Subjects will be divided randomly into two research groups, both will receive physiotherapy including mobility, strengthening and stretching exercises. Intervention group, additionally to exercises, will receive dry needling to the Gluteus Medius muscle by inserting a needle to a trigger point until a visible involuntary twitch in the muscle appears. Sham needling will be applied by needling with pre-cut and smoothed needles that will not penetrate the skin. Both groups will receive two treatments per week and up to six treatments overall, evaluation will be performed before and after the series of treatments.

Interventions

OTHERdry needling

dry needling for Gluteus Medius muscle in combination with exercises

OTHERsham dry needling

sham dry needling for Gluteus Medius muscle in combination with exercises

Sponsors

University of Haifa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

participants will not be aware of the group they were assigned

Intervention model description

two groups. research group will receive dry needling and control group will receive sham dry needling.

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Main complaint of nonspecific LBP over a 3 month period * VAS \> 3 at baseline

Exclusion criteria

* two or more of the following signs are present on physical examination: lower extremity weakness in a myotome distribution, decreased sensation in a dermatomal distribution, altered lower extremity deep tendon reflexes, pathological reflexes, a positive straight leg raise (SLR) test, crossed SLR or femoral nerve stretch test. * Symptoms began immediately after a significant trauma (motor vehicle accident, fall from a height) and subjects were not been screened for possible fractures. * Physical therapy or chiropractic treatment for LBP was provided during the 6 months prior to participation in the study or are currently being treated. * presence of contraindication for dry needling * pregnancy * past back or pelvic surgery

Design outcomes

Primary

MeasureTime frameDescription
change in visual analog scale (VAS)baseline and at 3 weeksassessing pain on a scale from 0 (no pain) to 10 (most sever pain). Higher scores means worse outcome.
Change in Modified Oswestry Disability Indexbaseline and at 3 weeksquestionnaire to assess the disability level associated with LBP and includes 10 questions regarding activities likely to be affected by LBP. Higher scores means worse outcome.
Global rating of change3 weeksa 15-point Likert scale ranging to assess treatment success. Higher scores mean a better outcome.

Secondary

MeasureTime frameDescription
Change in hip abductors muscle strengthbaseline and 3 weeksmuscle strength in Newton, assessed by an hand held dynamometer
Change in lumbar flexion range of motionbaseline and 3 weekslumbar flexion assessment by bending forward and measuring distance of fingers from the floor

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026