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A pilot randomised trial comparing a mindfulness-based stress reduction course, a locally-developed stress reduction intervention and a waiting list control group in a real-life municipal health care setting

机译:一个试点随机试验,比较了一个基于谨慎的压力还原过程,在现实的市政医疗保健环境中局部发育的应力减少干预和一名等候名单对照组

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摘要

Abstract Background The purpose of the present study was to conduct a pilot randomised controlled trial (RCT) to lend support to a larger effectiveness RCT comparing Mindfulness-Based Stress Reduction (MBSR), a locally-developed stress reduction intervention (LSR) and a waiting list control group in a Danish municipal health care center setting. Methods A three-armed parallel pilot RCT was conducted among 71 adults who contacted a Danish municipal health care center due to stress-related problems. Recruitment was made between January and April 2018 and followed usual procedures. Exclusion criteria: 1) acute treatment-demanding clinical depression or diagnosis of psychosis or schizophrenia, 2) abuse of alcohol, drugs, medicine, 3) pregnancy. Randomisation was performed by an independent data manager using the REDCap electronic data capture tool. The primary outcome was a description of RCT feasibility (recruitment and retention rates regarding intervention participation and 12-week follow-up). Secondary outcomes were completion rates regarding questionnaire data and proposed effect-estimates of outcome measures considered to be used in the following real RCT. Type of intervention and outcome assessment were not blinded. Results We recruited 71 of 129 eligible individuals from the target population (55, 95%CI: 46–64). Forty-two (59%) were females. Median age: 44 years (1-quartile:34, 3-quartile:50). Twenty-nine (41%) had < 16 years of education. Forty-eight (68%) were employed; 30 of these 48 (63%) were on sick leave. Mean scores for perceived stress (PSS): 25.4 ± 5.3; symptoms of anxiety and depression (SCL-5): 2.9 ± 0.6, and well-being (WHO-5): 31.7 ± 8.5 indicated a need for intervention. 16/24 (67, 95%CI: 45 to 84) who were allocated to MBSR and 17/23 (74, 95%CI: 52 to 90) who were allocated to LSR participated in ≥5 sessions. The loss to follow-up at 12 weeks: MBSR: 5 (21% (95% CI: 7 to 42), LSR: 5 (22% (95% CI: 7 to 44) and waiting list: 4 (17% (95% CI: 5 to 37). This was acceptable and evenly distributed. The results indicated MBSR to be superior. Conclusions An RCT assessing the effectiveness of stress reduction interventions in a real-life municipal health care setting is feasible among adults with a clear need for stress reduction interventions based on scores on mental health. Trial registration ClinicalTrials.gov. Identifier: NCT03663244 . Registered September 10, 2018.
机译:摘要本研究的目的是进行试验随机控制试验(RCT),以借出较大的有效性RCT对比较基于谨慎的应力减少(MBSR)的效果RCT,这是一种局部发育的应力减少干预(LSR)和等待列出丹麦市医疗保健中心设置的对照组。方法采用三武装平行的飞行员RCT在71名成人之间进行,由于压力有关的问题,他们与丹麦市医疗保健中心联系。 2018年1月至4月在2018年4月之间进行了招聘,并遵循通常的程序。排除标准:1)急性治疗急需临床抑郁或诊断精神病或精神分裂症,2)滥用酒精,药物,医药,3)妊娠。使用Redcap电子数据捕获工具由独立数据管理器执行随机化。主要结果是对RCT可行性的描述(关于干预参与和12周随访的招聘和保留率)。二次结果是关于调查问卷数据的完工率,并提出了考虑措施的估计,考虑在以下真正的RCT中使用。干预类型和结果评估没有蒙蔽。结果我们招聘了来自目标人口的129个符合条件的71名(55%,95%:46-64)。四十二(59%)是女性。中位年龄:44岁(1-四分位数:34,3-四分位数:50)。二十九(41%)有<16年的教育。雇用了四十八(68%);这48(63%)中的30个是病假。感知压力的平均分子(PSS):25.4±5.3;焦虑和抑郁症的症状(SCL-5):2.9±0.6,福祉(WHO-5):31.7±8.5表示需要干预。分配给MBSR和17/23(74,95%Ci:52至90)的16/24(67,95%CI:45至84)被分配给LSR的≥5个会议。在12周内进行随访:MBSR:5(21%(95%(95%CI:7至42),LSR:5(22%(95%(95%CI:7至44)和等待名单:4(17%)(17%)( 95%CI:5至37)。这是可接受的且均匀分布的。结果表明MBSR是优越的。结论将RCT评估了现实卫生保健环境中的压力减少干预措施的有效性,这是一个明确的成年人可行的需要基于精神健康的评分的压力减少干预。试验登记ClinicalTrials.gov。标识符:NCT03663244。2018年9月10日注册。

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