跳至主要内容
临床试验/NCT02890394
NCT02890394Unknown不适用

Effectiveness of the Suboccipital Inhibition Technique in Patients With Mechanical Neck Pain: a Pilot Study

University of Alcala0 个研究点目标入组 60 人开始时间: 2016年3月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
主要终点
Change from pain threshold pressure after ten minutes from the suboccipital inhibition

研究概览

简要总结

The project is based on checking the effectiveness of the technique of suboccipital inhibition in patients with mechanical neck pain. Suboccipital inhibition technique involves the placement of the hands of the physiotherapist under the patient's head so that fingers can feel the spinous processes of the cervical vertebrae. Then the fingers slowly leads upward to contact the occipital condyles. At this point the investigator should gently move your fingers down, finding the space between the condyles and the spinous process of the axis. Then, flexing the metacarpophalangeal joints at 90 degrees, slowly raises the skull. In this technique the investigator would be carrying out the relaxation of the suboccipital muscles: lower rectus capitis posterior, superior oblique head straight back and head higher. It is a technique used very often but without knowledge about the time needed for implementation. In several studies that have used the technique it has been maintained for 2.4 or 10 minutes without agreeing how long is necessary. The study will consist of three groups formed by patients with mechanical neck pain that they applied the technique two, four or ten minutes and a control group of patients with mechanical neck pain. The four groups were measured before and after treatment the pain threshold to pressure by algometer and conduct the test repositioning of the head to show any changes after application of the technique.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • Men and women of full age .
  • ≥ 15/50 rating in the Neck Disability Index
  • Participants with good adhesion to the study .
  • Participants who have signed informed after appropriate informed consent.

排除标准

  • Cancer , inflammatory , infectious , vascular , neurological and metabolic processes.
  • Patients who are under medical treatment.
  • Patients with psychiatric illnesses.
  • Women : pregnancy.
  • Patients who have not signed the informed consent.

结局指标

主要结局

Change from pain threshold pressure after ten minutes from the suboccipital inhibition

时间窗: It is measured at the beginning of the study. After ten minutes from the suboccipital inhibition is remeasured

Three measurements were performed with a rest period of 30 seconds between each measurement.

Change from repositioning of the head after ten minutes from the suboccipital inhibition

时间窗: It is measured at the beginning of the study. After ten minutes from the suboccipital inhibition is remeasured

a target is placed on the wall in front of the subject at a distance of 90 cm and adjusted to align with the reference position of the head. a helmet with a laser on top is used. For each test subjects will be instructed to memorize the initial reference position by carrying out a maximum cervical rotation and returning to the reference position without speed limit. Subjects undertake 10 trials. Before each test, the examiner manually reposition the subject's head to the reference position. Once the subject is instructed to conduct the test measurement.

次要结局

未报告次要终点

研究者

发起方
University of Alcala
申办方类型
Other
责任方
Principal Investigator
主要研究者

Alejandro Sánchez Tejada

Principal Investigator

University of Alcala

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