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Sensorimotor Control in People With and Without Neck Pain

2021年9月2日 更新者:CEU San Pablo University

Analysis of Sensorimotor Control in People With and Without Neck Pain Using Inertial Sensor Technology: Study Protocol for a Longitudinal Prospective Observational Study

This is a descriptive, observational, longitudinal, prospective study consecutively enrolling patients with non-specific neck pain and age-matched asymptomatic participants.

The investigators will register sensorimotor control variables, including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns. These variables will be recorded by means of Inertial Measurement Unit (IMU) sensors during the following tests consecutively performed in two measuring sessions separated by 12 months: (a) kinematics of planar movements, (b) kinematics of the craniocervical flexion movement, (c) kinematics during functional tasks and (d) kinematics of task-oriented neck movements in response to visual targets.

研究概览

研究类型

观察性的

注册 (预期的)

100

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Aitor Martin Pintado Zugasti, PhD
  • 电话号码:14691 91 3724700
  • 邮箱:martinpintado@ceu.es

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 65年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Patients will be recruited from a community sample in Madrid, Spain

描述

Inclusion Criteria:

  • Population aged between 18 and 65 years old

Exclusion Criteria:

  • Visual impairment not corrected by the use of glasses/contact lenses
  • Migraine headache
  • Complex regional syndrome
  • Previous surgeries in the neck and/or head region
  • Sensory and/or vestibular alterations, (f) Otogenic or idiopathic vertigo/dizziness
  • Presence of tumors in the craniocervical region
  • Previous fracture in the head or neck region
  • Osseous deformities in the thoracic, cervical or cranial region

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Asymptomatic participants
Asymptomatic subjects should not present any pain in the cervical region during the last 3 months and no previous treatment for neck pain in order to be included in the study.
Inertial Measurement Unit (IMU) sensors will measure sensorimotor control variables including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns
Neck pain patients
Patients with neck pain should have an intensity of pain of at least 3 points out of 10 on a Visual Analog Scale and a neck pain duration of at least 3 months of evolution. Neck pain could be from nonspecific mechanical origin, associated with whiplash or with a previous medical diagnosis of degenerative or inflammatory alterations of the cervical spine, associated or not with headache and pain in the shoulder region or the upper limb.
Inertial Measurement Unit (IMU) sensors will measure sensorimotor control variables including active range of motion, movement speed, acceleration, smoothness of motion, head repositioning accuracy and motion coupling patterns

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Active range of motion
大体时间:1 year
Expressed as an angular displacement (°) in 3 full-movements (flexion-extension, lateral flexion and rotation)
1 year
Movement speed
大体时间:1 year
Expressed as angular velocity (°/sec) in 3 full-movements (flexion-extension, lateral flexion and rotation)
1 year
Smoothness of motion
大体时间:1 year
expressed as movement jerk (º/sec3)
1 year
Head repositioning accuracy
大体时间:1 year
Calculated as the repositioning error considering the difference between the neutral starting position and the following positions reached after the performance of any of the movements
1 year
Motion coupling patterns
大体时间:1 year
Calculated as the angular displacement occurring in a different anatomical plane to the one that is being tested for each of the planar movements
1 year

次要结果测量

结果测量
措施说明
大体时间
Physical activity level
大体时间:1 year
Measured using the short version of the International Physical Activity Questionnaire (IPAQ). The score of the scale is expressed in MET level x minutes of activity/day x days per week. Levels of 3.3 METs are considered light, 4.0 METs are moderate and 8.0 METs are vigorous.
1 year
Fear of movement and injury
大体时间:1 year
Measured using the Tampa Scale for Kinesiophobia (TSK-11). It consists of 11 questions scored from 1 to 4. Therefore, a score of 11 is the lowest possible level of kinesiphobia, while 44 is the highest.
1 year
Pain-related fear-avoidance
大体时间:1 year
Measured using the Fear Avoidance Components Scale (FACS). It has 20 itemsmeasured on a 6-point Likert scale for total possible score of 100 and the lowest possible score of 0. Higher scores indicate higher levels of fear avoidance.
1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (预期的)

2021年10月10日

初级完成 (预期的)

2022年2月15日

研究完成 (预期的)

2023年2月15日

研究注册日期

首次提交

2021年8月31日

首先提交符合 QC 标准的

2021年8月31日

首次发布 (实际的)

2021年9月2日

研究记录更新

最后更新发布 (实际的)

2021年9月10日

上次提交的符合 QC 标准的更新

2021年9月2日

最后验证

2021年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • CEU-023

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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