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Assessing the effectiveness of enhanced psychological care for patients with depressive symptoms attending cardiac rehabilitation compared with treatment as usual (CADENCE): study protocol for a pilot cluster randomised controlled trial

机译:与常规治疗相比,评估对接受心脏康复治疗的抑郁症状患者进行加强心理护理的有效性(CADENCE):一项试验性集群随机对照试验的研究方案

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摘要

BACKGROUND: Around 17 % of people eligible for UK cardiac rehabilitation programmes following an acute coronary syndrome report moderate or severe depressive symptoms. While maximising psychological health is a core goal of cardiac rehabilitation, psychological care can be fragmented and patchy. This study tests the feasibility and acceptability of embedding enhanced psychological care, composed of two management strategies of proven effectiveness in other settings (nurse-led mental health care coordination and behavioural activation), within the cardiac rehabilitation care pathway. METHODS/DESIGN: This study tests the uncertainties associated with a large-scale evaluation by conducting an external pilot trial with a nested qualitative study. We aim to recruit and randomise eight comprehensive cardiac rehabilitation teams (clusters) to intervention (embedding enhanced psychological care into routine cardiac rehabilitation programmes) or control (routine cardiac rehabilitation programmes alone) arms. Up to 64 patients (eight per team) identified with depressive symptoms upon initial assessment by the cardiac rehabilitation team will be recruited, and study measures will be administered at baseline (before starting rehabilitation) and at 5 months and 8 months post baseline. Outcomes include depressive symptoms, cardiac mortality and morbidity, anxiety, health-related quality of life and service resource use. Trial data on cardiac team and patient recruitment, and the retention and flow of patients through treatment will be used to assess intervention feasibility and acceptability. Qualitative interviews will be undertaken to explore trial participants' and cardiac rehabilitation nurses' views and experiences of the trial methods and intervention, and to identify reasons why patients declined to take part in the trial. Outcome data will inform a sample size calculation for a definitive trial. DISCUSSION: The pilot trial and qualitative study will inform the design of a fully powered cluster randomised controlled trial to evaluate the effectiveness and cost-effectiveness of the provision of enhanced psychological care within cardiac rehabilitation programmes. TRIAL REGISTRATION: ISRCTN34701576 (Registered 29 May 2014).
机译:背景:在急性冠状动脉综合征后,符合英国心脏康复计划条件的人中,约有17%的人报告有中度或重度抑郁症状。虽然最大程度地提高心理健康是心脏康复的核心目标,但心理护理可能是零散的和零散的。这项研究测试了在心脏康复护理途径中嵌入增强型心理护理的可行性和可接受性,该方法由两种在其他情况下证明有效的管理策略(护士主导的精神保健协调和行为激活)组成。方法/设计:本研究通过嵌套定性研究进行外部试验,测试了与大规模评估相关的不确定性。我们的目标是招募和随机分配8个全面的心脏康复小组(小组)进行干预(将增强的心理护理纳入常规心脏康复计划中)或控制(仅常规心脏康复计划中)。将招募多达64位经​​心脏康复团队进行初步评估后确定为患有抑郁症状的患者(每组8位),并将在基线(开始康复之前)以及基线后5个月和8个月时实施研究措施。结果包括抑郁症状,心脏死亡率和发病率,焦虑症,与健康相关的生活质量和服务资源的使用。有关心脏团队和患者招募的试验数据,以及通过治疗的患者保留和流动情况,将用于评估干预的可行性和可接受性。将进行定性访谈,以探讨试验参与者和心脏康复护士对试验方法和干预措施的看法和经验,并确定患者拒绝参加试验的原因。结果数据将为确定的试验提供样本量计算信息。讨论:初步试验和定性研究将为全功能集群随机对照试验的设计提供参考,以评估心脏康复计划中提供增强心理护理的有效性和成本效益。试用注册:ISRCTN34701576(2014年5月29日注册)。

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