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临床试验/RBR-7m7ct53
RBR-7m7ct53已完成Unknown

Influence of spiritual well-being training on blood pressure control

iga de Hipertensão Arterial da Universidade Federal de Goiás0 个研究点开始时间: 2024年2月28日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方

研究概览

简要总结

Background: Spirituality, a comprehensive concept that encompasses personal aspects and interpersonal relationships, has been studied as a protector factor for cardiovascular diseases. As hypertension is the first cause of mortality worldwide, interventions that prove to be beneficial for its control and have few side effects, like human spirituality aspects, should be studied and considered for clinical practice. Methods: Randomized non-inferiority clinical trial with participants comprised of stage 1 and 2 hypertensive adults. After signing informed consent, individuals were randomized for intervention group (IG) ou control group (CG) and underwent a cardiologic consultation, which comprised anamnesis, including lifestyle habits and medications in regular use, measurement of peripheral and central blood pressure, home blood pressure monitoring (HBPM) and flow mediated dilation (FMD). IG received daily on WhatsApp, for 12 weeks, a message containing a video, a reflection message, or a task, all encouraging forgiveness, gratitude, optimism and life purpose. At the end of this period, all participants underwent the same procedures as of the initial visit. Results: Both groups were similar in all demographic aspects, except for the greater presence of women at the IG. Lifestyle habits and regular medications were not modified during the follow-up period. Comparison of the evaluated parameters between both groups demonstrated an improvement of FMD in the IG (increase from 9,8% to 14,3%) and worsening at CG (10,2% to 7,2%), p < 0,001. In addition, the peripheral systolic blood pressure (pSBP) drop was great and statistically significant in IG (7,6 mmHg) in comparison to CG (0,55 mmHg, p 0,848), and this variation was also statistically significant (p 0,047) when evaluated by student’s T test. Conclusion: The tool developed and used in this research allowed participants to work through beneficial feelings and was effective in improving FMD and pSBP to a similar or greater extent than other non-pharmacological measures or even some antihypertensive medications.

研究设计

研究类型
Interventional

入排标准

年龄范围
18Y 至 80Y(—)
性别
Female

入选标准

  • •Hypertensive adults (stage 1 or 2) with low and moderate cardiovascular risk, on stable use of antihypertensive medication for more than thirty days, evaluated by pressure measurements of the last visit.

排除标准

  • •Stage 3 patient hypertensive

研究者

发起方
iga de Hipertensão Arterial da Universidade Federal de Goiás

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