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临床试验/NCT05265468
NCT05265468已完成不适用

Noninvasive Treatment of Upper Trapezius Active Trigger Points in College Students With Neck Pain. A Randomized Clinical Trial

Universidad Católica San Antonio de Murcia1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2022年3月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
1
主要终点
Neck Disability Index

研究概览

简要总结

Hyperexcitable myofascial trigger points located within a taut band of skeletal muscle or fascia cause referred pain, local tenderness, and autonomic changes. The scientific data refer to an immediate improvement in the symptoms of these active points treated with manual therapy. Based on these factors, the objective of the study is to determine the effect of the combined therapy of the Jones, Chaitow, Lewit technique and pain-free positioning in participants with the presence of an active upper trapezius trigger point.

详细描述

The treatment will last a total of 15 minutes accompanied by a baseline assessment and after 10 minutes of the intervention in 3 experimental groups and a placebo group, of no-pain positioning. In addition to basic indices and scales of cervical pain and functionality, it is intended to measure flexibility, range of motion, proprioception and cognition through software with sensors of the latest technology when it comes to representing reliable results in differences between techniques.

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 (Care Provider, Outcomes Assessor)

入排标准

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

入选标准

  • •persistent neck pain or headache for more than 3 days
  • •presence of active trigger point in upper trapezius

排除标准

  • •Participants who present dizziness, vertigo and/or symptoms aggravated by the movement and/or positioning of the neck;
  • •who present infection or febrile state at the time of performing the test;
  • •with anxiety and/or extreme emotional tension;
  • •who are undergoing pharmacological treatment (analgesics, muscle relaxants, anxiolytics, antidepressants)

研究组 & 干预措施

Jones Group (Strain Counterstrain)

Experimental

Jones Group consist in 90 seconds in a ralease positioning of no pain in muscle acortation

干预措施: Jones Group (Strain Counterstrain) (Other)

Lewit Group

Active Comparator

Lewit Group consist in a maximum of four minutes of muscular contraction acompaind by stretching techniques

干预措施: Lewit Group (Other)

Chaitow Group

Active Comparator

Chaitow Group consist in a maximum of four minutes of muscular contraction acompaind by stretching techniques and deep diaphragmatic respiration

干预措施: Chaitow Group (Other)

Placebo Group

Placebo Comparator

Placebo Group only have to mantain no pain positioning for 3 minutes

干预措施: Placebo Group (Other)

结局指标

主要结局

Neck Disability Index

时间窗: 10 minutes

Self-completed neck questionnaire wich consists in 10 sections. Each one of them (cervical pain intensity, personal care, lifting weights, reading, headache, ability to concentrate, ability to work, driving, sleep and leisure activities) offers 6 possible answers that represent 6 progressive levels of functional capacity, and is scored from 0 to 5. The total score is expressed in percentage terms with respect to the maximum possible

Pain intensity

时间窗: 10 minutes

Measured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10

Pression algometer

时间窗: 10 minutes

Measures pressure pain thresholds

次要结局

  • Cervical Test(10 minutes)
  • Proprioceptive Test(10 minutes)

研究者

发起方
Universidad Católica San Antonio de Murcia
申办方类型
Other
责任方
Principal Investigator
主要研究者

Juan Martínez Fuentes

Study Director

Universidad Católica San Antonio de Murcia

研究点 (1)

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