Dry Needling and Functional Improvement

NCT ID: NCT02838394

Last Updated: 2024-04-25

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-12-31
• Study Completion Date: 2023-08-31

Brief Summary

Dry Needling (DN) is a skilled intervention that uses acupuncture filiform needles that are inserted into myofascial trigger points or other tissues underneath the skin. It is used to treat myofascial or neuromusculoskeletal pain and to improve movement impairments. Although more and more physical therapists add this treatment tool to their skill box, there is uncertainty about its working mechanism and its efficacy. The latter is partially due to the challenging task of finding and using a true control or sham treatment. The investigators will use blunted needles, which will not perforate the skin, as sham treatment.

This study will assess if DN of a trigger point in the gluteal muscles increases pain pressure threshold in that muscle, in another muscle innervated by the same segment (L4/5) and in an area not supplied by the same segment (i.e. the ipsilateral posterior shoulder). In addition, this study will assess if functionality, as measured by the Oswestry Disability Index (ODI) and 15-point Global Rating of Change Scale (GRoC) questionnaires, improves after 2-3 treatments (1 week) of DN.

Detailed Description

Background Dry Needling (DN) is a skilled intervention that uses acupuncture filiform needles that are inserted into myofascial trigger points or other tissues underneath the skin [Dunning]. Trigger points are spots in taut muscle fibers that can produce local and radiating pain when irritated, for example when pressed upon. Several theories on the etiology of trigger points exist, such as a local energy crisis and increased acetylcholine release due to mechanical muscle overuse [Bron]. The existence of trigger points is widely accepted [Hong], although there are also some vocal opponents [Quintner 2015, Quintner 1994].

The aim of DN is to treat myofascial or neuromusculoskeletal pain and improve movement impairments. The mechanism which with DN purportedly works has been the subject of debate for many years. It is generally accepted that the needle has to be inserted into a trigger point, where it will produce a local muscle twitch response and consequently 'inactivate' the trigger point [Dunning]. Some propose that the quick muscle contraction induces normalization of tissue pH and reduction of biochemical and neurotransmitters that stimulate pain receptors - a local response [Shah]. Others suggest that DN interrupts the trigger point's ongoing nociceptive input into the dorsal horn - a segmental response [Fernandez-de-las-Penas]. Others again submit that, because some trigger points affect limbic and dorsal hippocampus activity, DN might have a central response [Niddam].

The efficacy of DN is also not completely clear, but shows a trend. One early literature review and meta-analysis concluded that DN was not significantly superior to placebo control in regards to pain decrease [Tough]. However, since then several systematic reviews with meta-analyses [Tekin, Kietrys, Boyles] determined that the evidence suggested that DN for trigger point-derived pain was likely to be the most effective approach, was superior in decreasing pain compared to stretching and percutaneous electric nerve stimulation and at least as effective as manual trigger point release and other needling treatments. One literature analysis supports the use of DN not only for its immediate, but also short-term effectiveness in reducing pain in patients with upper quarter myofascial pain syndrome [Kietrys].

Controlled trials that assess DN efficacy either use 1) sham or control (such as no or an inactive treatment) or 2) other treatments (such as lidocaine injections, non-local DN, or "usual care", such as stretching and exercise) for the comparison group. A blunted needle that does not penetrate the skin is a good sham treatment [Streitberger] and has been recommended as adequate control. As discussed elsewhere [Streitberger], every needle penetration, be it at a trigger point or not, will induce physiological responses and are as such not appropriate to use as control.

Srbely et al. found that one intervention of trigger point stimulation with DN evoked palliative effects in other areas innervated by the same spinal segment. They dry needled trigger points in the supraspinatus and assessed pressure sensitivity changes in the infraspinatus (same segment, C5) and gluteus maximus (different segment, L4/5, S1). Their results suggest that pain pressure threshold was increased after 3 and 5 minutes of DN in the areas supplied by the C5 segment, but not in the area supplied by L4/5, S1.

The above named study only assessed immediate pain-related changes due to the intervention and did not assess functional improvements. The investigators of this study were not able to find any articles investigating this phenomenon in the lower extremity. This project will use a similar set up as the above study, but the subjects will receive sham DN, not real DN in a non-trigger point tissue (which, as explained above, will still elicit physiological effects and could have some segmental influence) as in the above named study. In addition, the investigators will explore if there are functional improvements in subjects receiving DN. Consequently, the investigators propose to perform the following controlled study that explores the questions 'Does site specific trigger point dry needling evoke segmental neuromodulation in the lower extremity and if so, do these changes make an impact on the subject's disability?'.

The aims are:

I) Regarding Pain

1. Assess if pain pressure threshold (PPT) decreases in the muscle that received DN

2. Assess if PPT decreases in the muscle that received sham DN (not perforating the skin)

3. Assess if low back pain decreases more in the treatment group compared to sham group

II) Regarding Functionality

1. Assess if the level of disability due to pain will be lower after one week of treatment in the subjects who received DN

2. Assess if the level of disability due to pain will be significantly lower in subjects who received DN compared to those who received sham

III) Regarding Mechanism

1. Assess if specific trigger point DN evokes segmental neuromodulation in the lower extremity; meaning that if a trigger point in a muscle that is innervated by a certain segment is DN, other trigger points in the same segment will exhibit decreased PPT as well.

2. Assess if PPT associated with trigger points in the infraspinatus change after DN the lower back

Our hypotheses are:

I)

• H1: PPT decreases in the gluteus maximus/medius after one week of DN
• H2: Trigger points that receive DN with sham needles (not perforating the skin) will not exhibit the same amount of decreased PPT compared to the trigger points that are DN with actual treatment DN

II)

• H3: Low back pain will decrease more in the treatment group compared to sham
• H4: The level of disability due to pain will decrease after one week of DN treatment
• H5: The level of disability due to pain will be significantly lower in subjects who received DN treatment compared to the subjects who received sham treatment

III)

• H6: Specific trigger point dry needling will evoke segmental neuromodulation in the lower extremity; meaning that if the investigators DN a trigger point in the gluteus maximus/medius, that are innervated by L4/L5, other trigger points in the same segment (i.e. multifidus at segment L4/5) will exhibit decreased PPT as well
• H7: PPT associated with trigger points in the infraspinatus will not change after DN the lower back Subjects will have been referred to Peaks Performance Physical Therapy (Baton Rouge, Louisiana) for diagnosis of 'trigger point gluteal muscles', 'myofascial pain', 'neuromuscular pain' or 'low back pain' (or similar) who demonstrate painful taut bands of tight muscle tissue in the gluteal muscles and infraspinatus and complain of radiating pain when point pressure is exerted onto that tight muscle tissue.

Methods

Prospective subjects will undergo physical examination by the co-author PC to identify inclusion and exclusion criteria.

The main inclusion criterion will be the presence of a painful trigger point in the gluteals (gluteus maximus or medius) and infraspinatus on the same side. The painful trigger point is defined as a distinct hypersensitive taut band within a muscle that begins to radiate diffuse pain into adjacent areas with sustained pressure. In keeping with the study conducted by Srbely et al. the investigators will only include trigger points with a baseline (pre-intervention) pain pressure threshold (PPT) value of 35 N or less in order to improve reliability of their detection. The precise location of each trigger point will be marked on the skin using a non-toxic marker for ease of follow-up identification.

If the patient is deemed eligible for the study, the investigating PT will explain the study to the prospective subject and he/she will be asked if he/she wants to participate. The PT will explain that the subject might not get the actual DN technique, but instead a sham. If the subject declines he/she will receive treatment as 'normal'. If he/she agrees, he/she will receive the informed consent to read and sign. If there are study-related questions they will be answered. After this the subject will fill out an intake sheet for demographic information, the modified Oswestry Disability Questionnaire (mOSW) [Copay] as well as a pain map and visual analog scale (VAS) for low back pain. The subject will then determine his/her group allocation by drawing a piece of paper out of an opaque envelope. This envelope will contain 40 pieces of paper; 20 of them will specify 'dry needling A' (for treatment), 20 will specify 'dry needling B' (for sham).

The rest of the physical therapy treatment will be pragmatic; the subject will receive mobilizations (no grade 5: high velocity low amplitude), exercises as indicated and DN for one week (2-3 visits). Grade 5 mobilizations (or manipulations) will be excluded as treatment option because they are believed to elicit neurophysiological effects, similar to DN, and might skew the results.

Study flow/ data intake

1. The investigators will measure pressure sensitivity via algometer in the gluteal muscles, the ipsilateral multifidus at level L4/5 and the ipsilateral infraspinatus.

2. The investigators will dry needle trigger points found in the gluteal region of one side (e.g. right) and document of muscle twitching (which would signify appropriate needle insertion) OR sham dry needle (with blunted needle, no actual penetration through the skin will occur)

3. Exercises will be performed as needed (pragmatic, but no manipulations). This regimen will be followed for maximally one week, (less, if pain is abolished).

4. At the end of the week PPT will be measured, VAS, the mOSW and the 15-point Global rating of change scales (GRoC) [Kamper] questionnaires will be given and results will be documented.

Data Analysis

PPT readings will be normalized to baseline scores so the focus is on the percent changes, not on the absolute changes in values.

• H1: baseline PPT measurements in the gluteus maximus/medius from 20 subjects who receive DN will be compared to post PPT measurements, taken after one week of DN will be analyzed using a paired t-test
• H2: change in PPT in the gluteus maximus/medius from 20 subjects who received DN will be compared to the change in PPT from 20 subjects who received sham DN will be analyzed with a 2-sample t-test
• H3: VAS score changes from 20 subjects who received DN will be compared to the VAS score changes from 20 subjects who received sham DN will be analyzed with a 2-sample t-test
• H4: The baseline mOSW scores from 20 subjects who received DN will be compared to the post treatment scores of the mOSW and will be analyzed with a paired t-test
• H5: The changes in mOSW and GRoC scale scores from 20 subjects who received DN will be compared to the changes in mOSW and GRoC scale scores from 20 subjects who received sham DN will each be analyzed with a 2-sample t-test
• H6: Pre- to post treatment changes in PPT in the gluteus maximus/medius will be compared to the changes measured in the multifidus at segment L4/5 and analyzed with a paired t-test
• H7: Pre- to post treatment changes in PPT in the gluteus maximus/medius will be compared to the changes measured in the infraspinatus and analyzed with a paired t-test

All significance levels will be set at 0.05. The minimally clinically important difference (MCID) for the VAS is 2 points [Childs], for the OSW it is 12.8 points [Copay] and the 'important improvement' for the GRoC is 5 points [Kamper].

Conditions

Myofascial Trigger Point Pain; Myofascial Pain Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Dry Needling

Trigger points found in the gluteal region of one side (e.g. right) will be dry needled; presence of muscle twitching (which would signify appropriate needle insertion) will be documented.

Group Type: EXPERIMENTAL

Dry needling

Intervention Type: PROCEDURE

Acupuncture filiform needles are inserted into myofascial trigger points

Sham Dry Needling

Trigger points found in the gluteal region of one side (e.g. right) will be SHAM dry needled with blunted needles, no actual penetration through the skin will occur.

Group Type: SHAM_COMPARATOR

Sham dry needling

Intervention Type: OTHER

Blunted needles will be pressed against the skin, but no actual penetration will occur

Interventions

Dry needling

Acupuncture filiform needles are inserted into myofascial trigger points

Intervention Type: PROCEDURE

Sham dry needling

Blunted needles will be pressed against the skin, but no actual penetration will occur

Intervention Type: OTHER

Other Intervention Names

Trigger point dry needling, intramuscular needling

Eligibility Criteria

Inclusion Criteria

• presence of at least one painful trigger point in the gluteals (gluteus maximus or medius) and infraspinatus on the same side.

Exclusion Criteria

• neurologic conditions (neuropathy, myopathy)
• use of medication (antidepressants, opioids) and/or acute cervico-thoracic injury (whiplash, facet irritation, acute discopathy) that could directly influence normal somatosensory processing at the C5 segment [Srbely]

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Brigham Young University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ulrike H Mitchell, PT, PhD

Role: PRINCIPAL_INVESTIGATOR

Brigham Young University

Locations

Brigham Young University Athletics

Provo, Utah, United States

Countries

United States

References

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Other Identifiers

16225

Identifier Type: -

Identifier Source: org_study_id