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首页> 外文期刊>BMC Pregnancy and Childbirth >Antenatal mindfulness intervention to reduce depression, anxiety and stress: a pilot randomised controlled trial of the MindBabyBody program in an Australian tertiary maternity hospital
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Antenatal mindfulness intervention to reduce depression, anxiety and stress: a pilot randomised controlled trial of the MindBabyBody program in an Australian tertiary maternity hospital

机译:产前正念干预以减少抑郁症,焦虑症和压力:澳大利亚三级妇产医院MindBabyBody计划的一项随机对照试验

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Background Mindfulness interventions to reduce psychological distress are well-suited to pregnancy, due to their brief and non-pharmacological nature, but there is a need for more robust evidence determining their usefulness. This pilot study was designed to explore the feasibility of a randomised controlled trial of a mindfulness intervention to reduce antenatal depression, anxiety and stress. Methods The study was designed in two parts 1) a non-randomised trial targeting women at risk of mental health problems (a selected population) and 2) a randomised controlled trial (RCT) of a universal population. Process evaluation focused on feasibility of recruitment pathways, participant retention, acceptability of study measures, and engagement with mindfulness practices. Measurement of psychological distress was taken pre and post intervention through the Centre for Epidemiologic Studies Depression Scale Revised, the Depression Anxiety and Stress Scale-21, the State-Trait Anxiety Inventory, and the Perceived Stress Scale. Results 20 women were recruited to the non-randomised trial, and 32 to the RCT. Recruitment through a mailed study brochure at the time of booking-in to the hospital resulted in the largest number of participants in the RCT (16/32; 50%), and resulted in considerably earlier recruitment (50% in first trimester, 50% second trimester) compared to recruitment through the antenatal clinic waiting room (86% in second trimester, 14% third trimester). Over a third of women in the universal population scored above clinical cut-offs for depression and anxiety, indicating a sample with more symptomology than the general population. The most common reason for loss to follow-up was delivery of baby prior to follow-up (n = 9). In the non-randomised study, significant within group improvements to depression and anxiety were observed. In the intervention arm of the RCT there were significant within group improvements to anxiety and mindfulness. No between group differences for the intervention and ‘care as usual’ control group were observed. Conclusions This small pilot study provides evidence on the feasibility of an antenatal mindfulness intervention to reduce psychological distress. Major challenges include: finding ways to facilitate recruitment in early pregnancy and engaging younger women and other vulnerable populations. Trial registration Australian New Zealand Clinical Trials Registry ACTRN12613000742774 webcite (31/10/2012).
机译:背景技术减少心理困扰的正念干预措施由于其短暂的和非药理的特性,非常适合怀孕,但需要更强有力的证据来确定其有效性。这项初步研究旨在探讨一项针对正念干预以减少产前抑郁,焦虑和压力的随机对照试验的可行性。方法该研究分为两个部分:1)针对有心理健康风险(选定人群)的女性的非随机试验,以及2)针对普遍人群的随机对照试验(RCT)。过程评估的重点是招聘途径的可行性,参与者的保留,研究措施的可接受性以及对正念实践的参与。心理痛苦的测量是通过流行病学研究中心修订的抑郁量表,抑郁焦虑和压力量表21,状态-特质焦虑量表以及感知的压力量表进行的。结果20名妇女被纳入非随机试验,32名妇女进入RCT。在预订医院时,通过邮寄的研究手册进行招募,导致参加RCT的人数最多(16/32; 50%),并且导致了相当早的招募(第一学期为50%,50%)与通过产前诊所候诊室招募相比(中期为86%,中期为14%)。普通人群中超过三分之一的女性在抑郁和焦虑方面的得分高于临床临界值,这表明该人群的症状学特征高于普通人群。失去随访的最常见原因是在随访之前分娩婴儿(n = 9)。在非随机研究中,观察到组内抑郁和焦虑明显改善。在RCT的干预部门中,小组内对焦虑和正念的改善显着。干预组和“照常护理”对照组之间没有差异。结论这项小型先导研究提供了产前正念干预措施减轻心理困扰的可行性的证据。主要挑战包括:寻找方法以促进早孕期的征兵,并使年轻妇女和其他脆弱人群参与进来​​。试验注册澳大利亚新西兰临床试验注册中心ACTRN12613000742774网站(31/10/2012)。

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