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Effects of Passive Hydrotherapy WATSU (WaterShiatsu) in the Third Trimester of Pregnancy: Results of a Controlled Pilot Study

机译:妊娠晚期的被动水疗法WATSU(WaterShiatsu)的效果:对照试验研究的结果

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摘要

Background. WATSU (WaterShiatsu) is a complementary therapeutic treatment method comprising passive stretches and massage techniques administered in 35°C warm water. Pregnant women claim safe methods to reduce pain, stress, and fatigue. Therefore, we conducted a pilot study evaluating the effects of WATSU on pregnancy-related complaints in third trimester pregnant women. Methods. Nine healthy pregnant women at gestational week ≥34 were included in an intervention group (receiving WATSU) and compared to eight women in a passive control group (receiving no treatment). WATSU was performed on days 1 and 4 of the study, accompanied by ultrasound examinations. Outcomes include physiological and psychometric as well as qualitative data. Participants in the control group completed questionnaires only. Results. WATSU was found to significantly lower participants' levels of stress and pain and to improve their mental health-related quality of life and mood. In comparison to the passive control group, participants in the intervention group reported reduction in perceived stress from day 1 to day 8 (P = 0.036, Cohen's f = 0.57). Qualitative data indicate that WATSU was appreciated as enjoyable and deeply relaxing. No negative side effects were reported. Conclusion. Our findings support the notion that WATSU yields therapeutic benefits for pregnant women and warrant further research. This study has been registered at ClinicalTrials.gov: .
机译:背景。 WATSU(WaterShiatsu)是一种补充性治疗方法,包括在35°C的温水中进行被动拉伸和按摩技术。孕妇声称可以减轻疼痛,压力和疲劳的安全方法。因此,我们进行了一项试点研究,评估WATSU对妊娠中期孕妇妊娠相关投诉的影响。方法。干预组(接受WATSU)中包括9名孕周≥34岁的健康孕妇,而被动对照组(未接受治疗)中有8名妇女。在研究的第1天和第4天进行WATSU,并进行超声检查。结果包括生理和心理测量以及定性数据。对照组参与者仅填写问卷。结果。发现WATSU可以显着降低参与者的压力和痛苦水平,并改善他们与心理健康相关的生活质量和情绪。与被动对照组相比,干预组的参与者报告说,从第1天到第8天,感觉到的压力有所减轻(P = 0.036,Cohen's f = 0.57)。定性数据表明,WATSU被认为是令人愉快且令人深感放松的。没有不良反应的报道。结论。我们的发现支持WATSU可以为孕妇带来治疗益处的观点,值得进一步研究。该研究已在ClinicalTrials.gov上注册:。

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