跳至主要内容
临床试验/NCT05939557
NCT05939557已完成不适用

Effects of Kinesio Taping vs Jones Technique on Myofascial Trigger Points in Cervicalgia: a Pilot Study of a Randomised Control Trial.

Blanca González Sanchez0 个研究点目标入组 38 人开始时间: 2015年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
38
主要终点
Change from Baseline VAS at 4 weeks of treatment and at the 2-week follow-up

研究概览

简要总结

A large number of workers in different sectors suffer from musculoskeletal neck disorders, which are the most common work-related illness in Europe. A multitude of combinations of techniques can be used to treat these conditions, including recorded film and the Jones technique. This pilot study examines the efficacy of Kinesio taping and the Jones technique in improving pain, joint range of motion and muscle tension in active subjects with latent myofascial trigger points. A clinical trial was conducted with 38 patients with neck pain. The sample was randomly distributed into three groups: a Jones technique group, a kinesio taping group and a combined therapy group in which both techniques were performed. The duration of treatment was 4 weeks, with a follow-up of 2 weeks. Cervical spine joint range of motion, pain and functional disability were assessed with the goniometer, the visual analogue scale, the pressure algometer and the cervical disability index.

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of latent PGM in the upper trapezius
  • Have been working for more than 6 months in the center or company
  • Work more than 4 hours a day with the computer
  • Be over 18 years of age and under 64 years of age

排除标准

  • Diagnosis of fibromyalgia
  • Having suffered a cervical sprain
  • Diagnosis of radiculopathy, cervical spine surgery
  • Medical contraindications to neuromuscular bandaging or Jones technique
  • Diseases such as diabetes and cancer, pregnancy, and any other pathology that produces neck pain other than that specified in the objective of the study

结局指标

主要结局

Change from Baseline VAS at 4 weeks of treatment and at the 2-week follow-up

时间窗: time 0, after 4 weeks of treatment, and at the 2-week follow-up

Visual Analogue Scale (VAS), consisting of a 10 cm line representing the continuous spectrum of painful experience. Only at the ends appear descriptions, "no pain" at one end and "worst pain imaginable" at the other, with no other description along the line. The subject will subjectively estimate his or her level of pain by indicating it on the ruler

Change from Baseline UDP at 4 weeks of treatment and at the 2-week follow-up

时间窗: time 0, after 4 weeks of treatment, and at the 2-week follow-up

Measurement of the pressure pain threshold (UDP) This is performed using a pressure algometer that aims to objectify the ability of muscle fibers to adapt to compression on underlying planes

Change from Baseline NDI at 4 weeks of treatment and at the 2-week follow-up

时间窗: time 0, after 4 weeks of treatment, and at the 2-week follow-up

Neck Disability Index (NDI), a questionnaire for self-assessment of function and activity disability in patients with neck pain. It consists of 10 items referring to functional activities, pain intensity, concentration and headache. The maximum score is 50 points, so that the higher the score the worse the function

Change from Baseline GONIOMETER at 4 weeks of treatment and at the 2-week follow-up

时间窗: time 0, after 4 weeks of treatment, and at the 2-week follow-up

Goniometer, instrument used for the study of joint mobility (MA). Cervical flexion, right and left lateralizations, and right and left rotations were evaluated. Each measurement was made three times with a separation of 30 seconds in time, taking the average between the three measurements.

次要结局

未报告次要终点

研究者

发起方
Blanca González Sanchez
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Blanca González Sanchez

PHD

University of Extremadura

相似试验

Effects of Kinesio Taping vs Jones Technique on... | 临床试验