Warm water

  • 文章类型: Journal Article
    背景:下腰痛(LBP)是最常见的身体疾病之一,其慢性表现是全球残疾的主要原因。在85%的病例中,LBP不能归因于已知的诊断,因此称为慢性非特异性LBP(cnLBP)。被动浸入温水通常被认为可以减轻肌肉紧张和疼痛,但尚未对CNLBP进行充分调查。当前的研究比较了三种被动水生干预措施对CNLBP的影响:漂浮(在漂浮装置上的仰卧浸没位置休息),WATSU(一种被动动手治疗,医生站在温水中,轻轻移动和按摩客户端),和Spa会议。
    方法:在这项随机交叉临床试验中,所有24名患有cnLBP的成年参与者将以平衡的顺序接受三项干预措施,其间至少有2周的洗脱期.评估将在研究的基线和随访以及每次干预之前和之后立即进行。评估涵盖自我报告的当前疼痛的主要结果(视觉模拟量表,范围:0-100毫米),其他自我报告问卷(地址,例如,人格特质或状态),和生理参数(例如,脊柱运动范围的测量)。
    结论:该研究增加了对CNLBP广泛的被动水生干预措施的干预措施特定效果大小的估计。该研究还指出了潜在的潜在的减轻疼痛机制。
    背景:该方案已获得伯尔尼州伦理委员会的批准(项目ID:2018-00461)。试验注册计划在ClinicalTrials.gov上进行。
    BACKGROUND: Low back pain (LBP) is among the most common physical ailments and its chronic manifestation is a leading cause for disability worldwide. LBP is not attributable to a known diagnosis in 85% of the cases and therefore called chronic non-specific LBP (cnLBP). Passive immersion in warm water is commonly claimed to reduce muscular tension and pain, but not yet sufficiently investigated with regard to cnLBP. The current study compares three passive aquatic interventions regarding their effects on cnLBP: floating (resting in a supine immersed position on flotation devices), WATSU (a passive hands-on treatment, in which a practitioner stands in warm water, gently moving and massaging the client), and a Spa session.
    METHODS: In this randomized cross-over clinical trial, all 24 adult participants with cnLBP will undergo the three interventions in balanced order with a washout-period of at least two weeks in between. Assessments will take place at baseline and follow-up of study and immediately before and after each intervention. Assessments cover the primary outcome self-reported current pain (Visual Analog Scale, range: 0-100 mm), other self-report questionnaires (addressing, e.g., personality traits or -states), and physiological parameters (e.g., measurement of spinal range of motion).
    CONCLUSIONS: The study adds estimates of intervention-specific effect-sizes of widespread passive aquatic interventions to cnLBP. The study also points to potential underlying pain-reducing mechanisms.
    BACKGROUND: The protocol was approved by the Ethics Committee of the Canton Bern (ProjectID: 2018-00461). Trial registration is intended at ClinicalTrials.gov.
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