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临床试验/NCT06891963
NCT06891963尚未招募不适用

Transcutaneous Electrical Nerve Stimulation Versus Dry Needling in Non Specific Chronic Neck Pain

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年3月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Assessment of neck pain intensity

研究概览

简要总结

This study aims to compare between the effectiveness of Acupuncture-Like Transcutaneous Electrical Nerve Stimulation (Acupuncture-like TENS) and dry needling on pain intensity, Pressure pain threshold (PPT) of upper trapezius myofascial trigger points, neck range of motion, and neck function in patients with non specific chronic neck pain.

详细描述

The incidence of myofascial trigger points (MTrPs) has been found to vary from 30% to 95% of people who have presented to pain treatment clinics. MPS is common and causes much disability and inability to work so that affect the economy and productivity of workers and employees. According to a previous study, physiotherapy is the most common method used to apply non-invasive techniques and may include the use of modalities for pain relief such as manual therapy, bracing, exercise, Electrical stimulation, kinesio tape, and ultrasound therapy and activity modification. Physiotherapy treatment is recommended to reduce pain, to restore range of motion, function and to strength and stabilize the spine .Trigger points may be relived through many non-pharmacological techniques such as spray and stretch transcutaneous electrical stimulation, massage and dry needing.

Electrotherapy has been widely used as a hypoalgesic agent, which typically involves transcutaneous nerve stimulation. Another well-known hypoalgesic technique is dry needling.

  • Acupuncture-Like Transcutaneous Electrical Nerve Stimulation (Acupuncture-like TENS): Acupuncture-like TENS
  • Acupuncture-like or Low frequency/High intensity TENS parameters include a low frequency (usually 1-4Hz), a high intensity (high enough to produce visible muscle contractions) and a long pulse duration (~200μs). Acupuncture-like TENS primarily stimulates the Group III (Aδ) and IV (C) nociceptive fibres and small motor fibres. As the mechanism of pain relief associated with this TENS mode requires afferent signals from muscle receptors, the electrodes should be positioned to produce visible muscle contractions, e.g. over a myotome related to the painful area. The user will therefore experience par aesthesia and muscle contraction (twitching type) with this mode. As muscle contractions occur, additional sensory information is carried from the muscle spindle via muscle afferents. This mode of TENS is believed to operate primarily through the release of endogenous opioids via the descending pain suppression system; therefore, there is a relatively longer onset to analgesia but the analgesia typically lasts longer with this mode than with Conventional TENS.

Dry needling (DN) uses a fine, solid needle and is also known as intramuscular stimulation clinical and scientific interest in DN has grown exponentially and various treatment effects are being credited to DN, such as: decreased pain and muscle tension, improved range of motion, muscle strength and coordination.

Although there are many previous studies on the effect of transcutaneous electrical nerve stimulation and dry needling on upper trapezius trigger points, there is no study comparing the therapeutic efficacy between them. However, till now no study compared the therapeutic potential of both modalities. So, this study will be conducted to compare between the effect of transcutaneous electrical nerve stimulation and dry needling in upper trapezius myofascial trigger point.

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
None

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Having at least 1 active trigger point in upper trapezius muscles will use a recommended diagnostic criterion to find active MTrPs which is:
  • •The presence of a palpable taut band in the skeletal muscle.
  • •The presence of a hypersensitive spot in the taut band.
  • •Local twitch response provoked by snapping palpation.
  • •Production of a typical referred pain pattern in response to the compression of tender spots.
  • •Spontaneous presence of the typical referred pain pattern.
  • •Duration of symptoms of acute stage (2-4) weeks.
  • •Age between (20-40) years.
  • •Having a normal neurological examination result .

排除标准

  • •Existence of cervical disc hernia, advanced cervical osteoarthritis, radiculopathy, or myelopathy.
  • •Having trigger point injection or physical therapy in the last 6 months.
  • •Having a rheumatologic disease, such as fibromyalgia, rheumatoid arthritis, or a hormonal disease, such as hypothyroidism, hyperthyroidism or hyperparathyroidism.
  • •Existence of kyphosis, scoliosis, forward head posture or cervicogenic headache.
  • •History of spine surgery.
  • •Having a cardiovascular problem.

研究组 & 干预措施

Acupuncture-like TENS + Conventional treatment

Experimental

This group will receive acupuncture like TENS with conventional treatment for 4 weeks.

干预措施: Acupuncture-like TENS (Other)

Acupuncture-like TENS + Conventional treatment

Experimental

This group will receive acupuncture like TENS with conventional treatment for 4 weeks.

干预措施: Conventional treatment (Other)

Dry needling + Conventional treatment

Experimental

This group will receive dry needling with conventional treatment for 4 weeks.

干预措施: Conventional treatment (Other)

Dry needling + Conventional treatment

Experimental

This group will receive dry needling with conventional treatment for 4 weeks.

干预措施: Dry needling (Other)

Conventional treatment

Active Comparator

This group will receive conventional treatment for 4 weeks.

干预措施: Conventional treatment (Other)

结局指标

主要结局

Assessment of neck pain intensity

时间窗: 4 weeks

The Visual Analogue Scale (VAS) will be used to evaluate pain intensity. It is a horizontal line whose length is 10 cm; its left end (zero) indicates no pain, while its right end (ten) reveals the worst imaginable pain. Each subject will be in relaxed position and will be asked to mark the point on the line that exactly corresponded to his/her pain.

Assessment of pressure pain threshold (PPT)

时间窗: 4 weeks

The pressure pain threshold (PPT) will be assessed by positioning the tip of the algometer on the trigger point and increasing the pressure by 1 kg per second. When the patient indicates discomfort, the pressure value will be recorded in kg/cm. The procedure will be repeated three times at 60 s intervals, and the mean pressure value will be recorded as the PPT.

次要结局

  • Measurement of cervical extension ROM(4 weeks)
  • Measurement of cervical lateral flexion to the right ROM(4 weeks)
  • Measurement of cervical flexion range of motion (ROM)(4 weeks)
  • Measurement of cervical lateral flexion to the left ROM(4 weeks)
  • Measurement of cervical rotation to the right ROM(4 weeks)
  • Measurement of cervical rotation to the left ROM(4 weeks)
  • Assessment of neck function(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sara Galal Mohamed Soliman

Principal Investigator

Cairo University

研究点 (1)

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