跳至主要内容
临床试验/NCT04060004
NCT04060004已完成不适用

The Effects of Dry Needling on the Superficial Neck Musculature in Patients With Chronic Myofascial Pain: A Randomized Controlled Trial

University of Valladolid2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年9月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Motor control

研究概览

简要总结

The term myofascial pain refers to the existence of myofascial trigger points (MTP), which are defined as hypersensitive points in a tense band of skeletal muscle, which can cause referred pain or autonomous phenomena.

To address the treatment of myofascial trigger points, conservative and invasive techniques have been proposed. Dry needling is one of the invasive techniques that have been shown to be effective in improving pain and function in patients with myofascial trigger points.

This trial aims to analyse the effectiveness of dry needling in patients with myofascial neck pain.

详细描述

The main objective of the study is to analyze the effects of dry needling on the superficial neck musculature in patients with chronic myofascial neck pain in terms of pain, functional capacity, mobility, psychosocial variables and motor control compared with both sham dry needling group and control group.

In addition, a secondary objective is to analyze the relationships between the psychosocial variables and the results obtained in the variables analyzed in the patients belonging to the three groups.

For this purpose the investigators conduct a randomized controlled trial double-blind. Patients included are randomized into 3 groups. One receives dry needling, another one receives sham dry needling, and the last one is a control group.

The hypothesis of this study is that patients in the real dry needling group will improve more compared to patients in the sham dry needling group and the control group.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with myofascial neck pain
  • Presence of at least one active myofascial trigger point on the superficial neck musculature
  • Neck pain of at least 3 months
  • Age 18-70
  • Pain intensity between 20 and 100 mm in the Analog Visual Scale
  • Neck disability index (NDI) greater than or equal to 15 points
  • Spanish speakers
  • Patients who do not present contraindications for the use of dry needling (anticoagulants, nickel allergy or belenophobia)
  • Patients who have not received physiotherapy or pharmacological treatment for neck pain for the last three months

排除标准

  • History of cervical trauma
  • Cervical spine surgery
  • Vertebral fracture
  • Cervical pain associated with whiplash
  • Red flags (tumor, metabolic disorders or rheumatoid arthritis)
  • Inflammatory lesion in the neck region
  • Pregnancy
  • Fibromyalgia diagnosis
  • Neck pain associated with radiculopathy
  • Patients pending legal litigation
  • Psychiatric pathology diagnosis

结局指标

主要结局

Motor control

时间窗: Through study completion, an average 11 days.

The investigators measure the motor control with Craniocervical Flexion Test (CCFT) at the end of the intervention (through study completion, an average 11 days).

Neck pain

时间窗: Through study completion, an average of 11 days.

The investigators measure the neck pain with Visual Analogue Scale (VAS) at the end of the intervention (through study completion, an average 11 days).

Cervical disability

时间窗: Through study completion, an average 11 days.

The investigators measure the cervical disability with Neck Disability Index (NDI) at the end of the intervention (through study completion, an average 11 days).

次要结局

  • Pressure pain threshold(Through study completion, an average 11 days.)
  • Pain catastrophism(Through study completion, an average 11 days.)
  • Neck range of motion(Through study completion, an average 11 days.)
  • Anxiety and depression(Through study completion, an average 11 days.)
  • Kinesiophobia(Through study completion, an average 11 days.)

研究者

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

Ricardo Medrano de la Fuente

Physiotherapist

University of Valladolid

研究点 (2)

Loading locations...

相似试验