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临床试验/NCT02164123
NCT02164123已完成不适用

Autonomic Effects of T4 Mobilization in Asymptomatic Subjects: Randomized Clinical Trial

Federal University of Health Science of Porto Alegre1 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2014年7月1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
86
试验地点
1
主要终点
Skin conductance

研究概览

简要总结

The purpose of this study is to determine whether passive accessory intervertebral mobilization applied to the fourth thoracic vertebra produces autonomic effects.

详细描述

Asymptomatic subjects will be recruited to this study. Pressure pain threshold, heart rate, heart rate variability and skin conductance will be measured before, immediately after and fifteen minutes after the intervention.

Subjects will be randomized into three groups: Passive accessory intervertebral mobilization one, passive accessory intervertebral mobilization two and placebo group.

The researcher that will do the intervention will be blinded to the outcomes measures, and the researcher that will do the measurements will be blind to the intervention.

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 (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • •Asymptomatic subjects
  • •Aged between 18 - 40 years old
  • •Portuguese readers and writers

排除标准

  • •History of lesion or surgery to the spine

研究组 & 干预措施

Spinal mobilization

Experimental

20 subjects will be randomized to this arm. A postero-anterior (PA) mobilization, to the fourth thoracic vertebra will be applied, for 3 sets of one minute. The subject will be comfortable prone lying.

干预措施: Spinal mobilization (Other)

Spinal Mobilization II

Active Comparator

20 subjects will be randomized to this arm. A postero-anterior (PA) mobilization, to the fourth thoracic vertebra will be applied, for 3 sets of one minute, but in this case, the subject will be seated, in a position that influence the sympathetic trunk, at the thorax.

干预措施: Spinal Mobilization II (Other)

Placebo

Placebo Comparator

20 subjects will be randomized to this arm. Only manual contact will be applied, without any oscillation. The subject will be comfortable prone lying. The intervention time is the same of the other arms.

干预措施: Placebo (Other)

结局指标

主要结局

Skin conductance

时间窗: Change from Baseline imediately after, and 15 minutes after the intervention

Skin conductance will be measured with Biopac MP150, the electrodes will be attached to the third and fourth fingers bilaterally. This measurement will be made during all the procedure, before, during and until 15 minutes after the intervention.

次要结局

  • Pressure pain threshold(Change from Baseline imediately after, and 15 minutes after the intervention)

研究者

发起方
Federal University of Health Science of Porto Alegre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Francisco Xavier de Araujo, Pt

Pt

Federal University of Health Science of Porto Alegre

研究点 (1)

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