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?
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- pressure sensitivity (pain pressure threshold)
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •presence of at least one painful trigger point in the gluteals (gluteus maximus or medius) and infraspinatus on the same side.
排除标准
- •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]
研究组 & 干预措施
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.
干预措施: Dry needling (Procedure)
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.
干预措施: Sham dry needling (Other)
结局指标
主要结局
pressure sensitivity (pain pressure threshold)
时间窗: 1 week
Pain pressure threshold values as measured with algometer
次要结局
- modified Oswestry Disability Questionnaire (mOSW)(1 week)
- 15-point Global Rating of Change Scale (GRoC)(1 week)
- Low back pain as measured with visual analog scale (VAS)(1 week)
