Effectiveness Comparison of Thoracic Thrust Manipulation in People With Neck or Low Back Pain
Comparison of the Effectiveness of the Thoracic Thrust Manipulation in People With Neck or Low Back Pain
Objective:
To compare the effectiveness of thoracic thrust manipulation, together with massages techniques and stretching, between people with neck pain versus people with low back pain.
Methods:
The research will be performed from August 2021 to October 2021 at the University of Alcala de Henares. (Madrid)
A minimum of forty-six (46) volunteers will participate in this research, and they will be divided in two groups of twenty-three (23). One group will be formed by candidates suffering from neck pain (group A) and the other one by candidate with low back pain (group B).
Both groups will receive the same treatment and specific stretching exercises as applicable in accordance to the pain area, e.g.: group A will get the massage and the stretching exercises more suitable for the neck pain and group B the same but for the low back pain. Nevertheless both groups will receive the same technical thrust manipulation in thoracic area.
All these treatments will be applied of the volunteers at the University of Alcalá.
The treatment includes the following activities:
- Twenty (20) minutes massage in the pain area, as applicable.
- Technical thrust manipulation in thoracic area.
- Ten (10) minutes stretching in accordance to the pain area treated. The stretching shall be repeated twice a week by each volunteer.
A total of six (6) sessions will be carried out during six (6) weeks, one session per week.
Pain, disability, kinesiophobia, HRQoL will be assessed as follow:
- Before first session. (In this evaluation will be also analyzed demographic variables i.e.: height, weight, age, gender, academic level, smoker/no smoker)
- Between third and fourth session.
- After sixth session.
- Four weeks after sixth session.
研究概览
地位
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
Madrid
-
Alcalá De Henares、Madrid、西班牙、28801
- Alicia Masip
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Age between 18 and 65 years
- Non-specific neck/low back pain for the last three (3) months before the first session.
Exclusion Criteria:
- Previous surgery in the areas covered by this research (neck and/or low back)
- Red flags: Cancer or tumor, fracture...
- Scoliosis or osteoporosis
- Neck or low back pain with radiculopathy symptoms
- Central nervous system involvement
- Fear to manipulation
- Neck pain associated with whiplash injuries on the last six (6) months
- Pregnant women
- Not understand, write and speak Spanish fluently
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:A group: neck pain
|
|
|
实验性的:B group: low back pain
|
|
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 |
|---|---|---|
|
Change in Neck and Low Back Pain
大体时间:Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
using a Visual Analogue Scale (VAS) from 0 to 10
|
Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in Neck Pain related disability
大体时间:Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
Using the Neck Disability Index (NID) Questionnaire
|
Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
|
Change in Health related quality of life (HRQoL)
大体时间:Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
Using the SF-12 Quality of Life Questionnaire
|
Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
|
Change in kinesiophobia
大体时间:Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
Using the fear avoidance beliefs (FAB) questionnaire
|
Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
|
Change in Low Back Pain related disability
大体时间:Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
Using the Oswestry Disability Index (ODI) Questionnaire
|
Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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