Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, BS8 1NU, UK.
Liggins Institute, University of Auckland, Auckland, 1142, New Zealand.
Trials. 2023 Feb 27;24(1):147. doi: 10.1186/s13063-023-07084-8.
People living with Parkinson's disease experience progressive motor and non-motor symptoms, which negatively impact on health-related quality of life and can lead to an increased risk of hospitalisation. It is increasingly recognised that the current care models are not suitable for the needs of people with parkinsonism whose care needs evolve and change as the disease progresses. This trial aims to evaluate whether a complex and innovative model of integrated care will increase an individual's ability to achieve their personal goals, have a positive impact on health and symptom burden and be more cost-effective when compared with usual care.
This is a single-centre, randomised controlled trial where people with parkinsonism and their informal caregivers are randomised into one of two groups: either PRIME Parkinson multi-component model of care or usual care. Adults ≥18 years with a diagnosis of parkinsonism, able to provide informed consent or the availability of a close friend or relative to act as a personal consultee if capacity to do so is absent and living in the trial geographical area are eligible. Up to three caregivers per patient can also take part, must be ≥18 years, provide informal, unpaid care and able to give informed consent. The primary outcome measure is goal attainment, as measured using the Bangor Goal Setting Interview. The duration of enrolment is 24 months. The total recruitment target is n=214, and the main analyses will be intention to treat.
This trial tests whether a novel model of care improves health and disease-related metrics including goal attainment and decreases hospitalisations whilst being more cost-effective than the current usual care. Subject to successful implementation of this intervention within one centre, the PRIME Parkinson model of care could then be evaluated within a cluster-randomised trial at multiple centres.
帕金森病患者会经历进行性的运动和非运动症状,这会对健康相关的生活质量产生负面影响,并导致住院风险增加。人们越来越认识到,当前的护理模式并不适合帕金森病患者的需求,因为他们的护理需求会随着疾病的进展而不断变化。本试验旨在评估综合护理的复杂创新模式是否会提高个人实现个人目标的能力,对健康和症状负担产生积极影响,并在与常规护理相比时更具成本效益。
这是一项单中心、随机对照试验,将帕金森病患者及其非专业照护者随机分为两组:PRIME 帕金森多组分护理模式或常规护理。年龄≥18 岁、诊断为帕金森病、能够提供知情同意或如果没有能力,则有亲密朋友或亲戚作为个人顾问、且居住在试验地理区域的成年人有资格参加。每位患者最多可有 3 名照护者参加,必须年满 18 岁,提供非专业、无报酬的护理,并能够提供知情同意。主要结局指标是目标实现,使用班戈目标设定访谈进行测量。登记的持续时间为 24 个月。总招募目标为 n=214,主要分析将采用意向治疗。
本试验测试了一种新的护理模式是否可以改善健康和疾病相关指标,包括目标实现,并减少住院治疗,同时比当前的常规护理更具成本效益。在一个中心成功实施该干预措施的前提下,PRIME 帕金森护理模式随后可以在多个中心的集群随机试验中进行评估。