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Advancing Symptom Alleviation with Palliative Treatment (ADAPT) trial to improve quality of life: a study protocol for a randomized clinical trial

机译:推进症状缓解姑息治疗(适应)审判以提高生活质量:随机临床试验的研究方案

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People living with chronic heart failure (CHF), chronic obstructive pulmonary disease (COPD), and interstitial lung disease (ILD) suffer impaired quality of life due to burdensome symptoms and depression. The Advancing Symptom Alleviation with Palliative Treatment (ADAPT) trial aims to determine the effect of a multidisciplinary, team-based intervention on quality of life in people with these common diseases. The ADAPT trial is a two-site, patient-level randomized clinical trial that examines the effectiveness of the ADAPT intervention compared to usual care on patient-reported quality of life at 6?months in veterans with CHF, COPD or ILD with poor quality of life and increased risk for hospitalization or death. The ADAPT intervention involves a multidisciplinary team-a registered nurse, social worker, palliative care specialist, and primary care provider (with access to a pulmonologist and cardiologist)-who meet weekly to make recommendations and write orders for consideration by participants' individual primary care providers. The nurse and social worker interact with participants over six visits to identify and manage a primary bothersome symptom and complete a structured psychosocial intervention and advance care planning. The primary outcome is change in patient-reported quality of life at 6 months as measured by the Functional Assessment of Chronic Illness Therapy-General questionnaire. Secondary outcomes at 6 months include change in symptom distress, depression, anxiety, disease-specific quality of life hospitalizations, and advance care planning communication and documentation. Intervention implementation will be assessed using a mixed-methods approach including a qualitative assessment of participants' and intervention personnel experiences and a quantitative assessment of care delivery, resources, and cost. The ADAPT trial studies an innovative intervention designed to improve quality of life for veterans with common, burdensome illnesses by targeting key underlying factors-symptoms and depression-that impair quality of life but persist despite disease-specific therapies. Leveraging the skills of affiliate health providers with physician supervision will extend the reach of palliative care and improve quality of life for those with advanced disease within routine outpatient care. The hybrid effectiveness/implementation design of the ADAPT trial will shorten the time to broader dissemination if effective and create avenues for future research. ClinicalTrials.gov, NCT02713347 . Registered March 19, 2016.
机译:患有慢性心力衰竭(CHF),慢性阻塞性肺病(COPD)和间质肺病(ILD)的人因繁重的症状和抑郁而遭受的生活质量受损。通过姑息治疗(适应)试验的推进症状减轻旨在确定多学科,基于团队的干预对患有这些常见疾病的人们的生活质量的影响。适应试验是一个双地,患者水平随机临床试验,审查了适应性干预的有效性,与常规关心患者报告的患者报告的生活质量为6?几个月,具有劣质,对质量差生活和住院或死亡风险增加。适应干预涉及多学科团队 - 一个注册护士,社会工作者,姑息护理专家和初级护理提供者(通过访问肺病学家和心脏病专家) - 每周满足谁,以提出建议和写订单,供参与者个人初级保健审议提供者。护士和社会工作者与参与者互动,以六次访问,以识别和管理初级麻醉症状,并完成结构化的心理社会干预和提前关怀规划。由于慢性疾病治疗常规调查问卷的功能评估来衡量,主要结果是患者报告的患者报告的生活质量的变化。 6个月的次要结果包括症状痛苦,抑郁,焦虑,疾病特异性生活质量的变化,以及提前关注规划沟通和文件。使用混合方法方法评估干预实施,包括对参与者和干预人员经验的定性评估以及对护理,资源和成本的定量评估。适应试验研究了一种创新干预,旨在通过针对关键的潜在因素和抑郁症来改善常见,繁重的疾病的生活质量 - 症状和抑郁 - 尽管有疾病特异性疗法,但损害了生活质量,但持续存在。利用医生监督的联盟卫生供应商的技能将延长姑息治疗的覆盖力,提高常规门诊护理中具有晚期疾病的人的生活质量。如果有效和创建未来研究的途径,适应试验的混合效率/实施设计将缩短更广泛传播的时间。 ClinicalTrials.gov,NCT02713347。注册2016年3月19日。

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