Brealey Stephen, Armstrong Alison L, Brooksbank Andrew, Carr Andrew Jonathan, Charalambous Charalambos P, Cooper Cushla, Corbacho Belen, Dias Joseph, Donnelly Iona, Goodchild Lorna, Hewitt Catherine, Keding Ada, Kottam Lucksy, Lamb Sarah E, McDaid Catriona, Northgraves Matthew, Richardson Gerry, Rodgers Sara, Shah Sarwat, Sharp Emma, Spencer Sally, Torgerson David, Toye Francine, Rangan Amar
York Trials Unit, Department of Health Sciences, Faculty of Sciences, University of York, ARRC Building, York, YO10 5DD, UK.
University Hospitals of Leicester NHS Trust, Leicester General Hospital, Gwendolen Road, Leicester, LE5 4PW, UK.
Trials. 2017 Dec 22;18(1):614. doi: 10.1186/s13063-017-2352-2.
Frozen shoulder (also known as adhesive capsulitis) occurs when the capsule, or the soft tissue envelope around the ball and socket shoulder joint, becomes scarred and contracted, making the shoulder tight, painful and stiff. It affects around 1 in 12 men and 1 in 10 women of working age. Although this condition can settle with time (typically taking 1 to 3 years), for some people it causes severe symptoms and needs referral to hospital. Our aim is to evaluate the clinical and cost-effectiveness of two invasive and costly surgical interventions that are commonly used in secondary care in the National Health Service (NHS) compared with a non-surgical comparator of Early Structured Physiotherapy.
We will conduct a randomised controlled trial (RCT) of 500 adult patients with a clinical diagnosis of frozen shoulder, and who have radiographs that exclude other pathology. Early Structured Physiotherapy with an intra-articular steroid injection will be compared with manipulation under anaesthesia with a steroid injection or arthroscopic (keyhole) capsular release followed by manipulation. Both surgical interventions will be followed with a programme of post-procedural physiotherapy. These treatments will be undertaken in NHS hospitals across the United Kingdom. The primary outcome and endpoint will be the Oxford Shoulder Score (a patient self-reported assessment of shoulder function) at 12 months. This will also be measured at baseline, 3 and 6 months after randomisation; and on the day that treatment starts and 6 months later. Secondary outcomes include the Disabilities of Arm Shoulder and Hand (QuickDASH) score, the EQ-5D-5 L score, pain, extent of recovery and complications. We will explore the acceptability of the different treatments to patients and health care professionals using qualitative methods.
The three treatments being compared are the most frequently used in secondary care in the NHS, but there is uncertainty about which one works best and at what cost. UK FROST is a rigorously designed and adequately powered study to inform clinical decisions for the treatment of this common condition in adults.
International Standard Randomised Controlled Trial Register, ID: ISRCTN48804508 . Registered on 25 July 2014.
肩周炎(也称为粘连性关节囊炎)是指肩关节球窝周围的关节囊或软组织包膜发生瘢痕形成和挛缩,导致肩部紧绷、疼痛和僵硬。在工作年龄段的男性中,约每12人中有1人受其影响;女性中,约每10人中有1人受其影响。虽然这种情况可能会随着时间自行缓解(通常需要1至3年),但对一些人来说,它会导致严重症状,需要转诊至医院。我们的目的是评估两种侵入性且昂贵的手术干预措施的临床效果和成本效益,这两种措施在英国国家医疗服务体系(NHS)的二级医疗中常用,同时与非手术对照措施早期结构化物理治疗进行比较。
我们将对500例临床诊断为肩周炎且X线片排除其他病变的成年患者进行一项随机对照试验(RCT)。将早期结构化物理治疗联合关节内类固醇注射与麻醉下手法松解联合类固醇注射或关节镜(锁孔)关节囊松解并随后进行手法松解进行比较。两种手术干预措施之后都将进行术后物理治疗方案。这些治疗将在英国各地的NHS医院进行。主要结局和终点将是12个月时的牛津肩部评分(一种患者自我报告的肩部功能评估)。在基线、随机分组后3个月和6个月;以及治疗开始当天和6个月后也将进行测量。次要结局包括手臂、肩部和手部功能障碍(QuickDASH)评分、EQ-5D-5L评分、疼痛、恢复程度和并发症。我们将使用定性方法探讨不同治疗方法对患者和医疗保健专业人员的可接受性。
所比较的三种治疗方法是NHS二级医疗中最常用的,但哪种方法效果最佳以及成本如何尚不确定。英国肩周炎随机对照试验(UK FROST)是一项设计严谨且样本量充足的研究,可为成人这种常见疾病的临床治疗决策提供依据。
国际标准随机对照试验注册库,编号:ISRCTN48804508。于2014年7月25日注册。