Østerås Nina, Hagen Kåre Birger, Grotle Margreth, Sand-Svartrud Anne-Lene, Mowinckel Petter, Aas Eline, Kjeken Ingvild
National Advisory Unit on Rehabilitation in Rheumatology, Diakonhjemmet Hospital, Oslo, PO Box 23 Vindern, N-0319 Oslo, Norway.
BMC Musculoskelet Disord. 2014 Mar 14;15:82. doi: 10.1186/1471-2474-15-82.
Hand osteoarthritis (OA) is one of the most prevalent musculoskeletal diseases in an adult population and may have a large influence on an individual's functioning, health-related quality of life and participation in society. Several studies have demonstrated that exercises may reduce pain and improve functioning in people with knee OA, with a similar effect suggested for hip OA. For hand OA, available research is very limited and shows conflicting results, and high-quality randomised controlled trials are warranted.This paper outlines the protocol for a randomised controlled trial that aims to determine the effect of an exercise intervention on self-reported hand activity performance in people with hand OA.
Participants with physician-confirmed hand OA according to the ACR clinical criteria are being recruited from two Norwegian OA cohorts: the population-based "Musculoskeletal pain in Ullensaker Study" (MUST) OA cohort, and the hospital-based Oslo Hand OA cohort. Participants are randomised into an intervention- or control group. The control group receives "usual care", whereas the intervention group receives a 12-week exercise intervention. The intervention group attends four group sessions and is instructed to perform the exercise program three times a week at home. Adherence will be captured using self-report. During the eight weeks with no group sessions, the intervention group receives a weekly telephone call. The assessments and group sessions are being conducted locally in Ullensaker Municipality and at Diakonhjemmet Hospital, Oslo. Outcomes are collected at baseline, and at 3 and 6 months. The primary outcome measure is self-reported hand activity performance at 3 months post-randomisation, as measured by the Functional Index for Hand Osteoarthritis (FIHOA); and a patient-generated measure of disability, the Patient-Specific Functional Scale (PSFS). Secondary outcome measures are self-reported OA symptoms (e.g. pain, stiffness and fatigue), the Patient Global Assessment of disease activity, measured hand function (e.g. grip strength, thumb web space and hand dexterity) and health-related quality of life. Cost-utility and cost-effectiveness analyses will be conducted.
This study will contribute to the knowledge on both the effect and resource use of an exercise programme with telephone follow-up on self-reported hand activity performance among people with hand OA.
The trial is registered at ClinicalTrials.gov with registration number: NCT01245842.
手部骨关节炎(OA)是成年人群中最常见的肌肉骨骼疾病之一,可能对个体的功能、健康相关生活质量及社会参与产生重大影响。多项研究表明,运动可减轻膝关节OA患者的疼痛并改善其功能,髋关节OA患者也有类似效果。对于手部OA,现有研究非常有限且结果相互矛盾,因此需要高质量的随机对照试验。本文概述了一项随机对照试验的方案,旨在确定运动干预对手部OA患者自我报告的手部活动表现的影响。
根据美国风湿病学会(ACR)临床标准,经医生确诊为手部OA的参与者正从两个挪威OA队列中招募:基于人群的“乌伦萨克肌肉骨骼疼痛研究”(MUST)OA队列和基于医院的奥斯陆手部OA队列。参与者被随机分为干预组或对照组。对照组接受“常规护理”,而干预组接受为期12周的运动干预。干预组参加四次小组课程,并被要求每周在家中进行三次运动计划。依从性将通过自我报告来记录。在没有小组课程的八周内,干预组每周会接到一次电话。评估和小组课程在乌伦萨克市当地以及奥斯陆的迪亚科内赫门特医院进行。在基线、3个月和6个月时收集结果。主要结局指标是随机分组后3个月时自我报告的手部活动表现,通过手部骨关节炎功能指数(FIHOA)进行测量;以及患者生成的残疾测量指标,即患者特定功能量表(PSFS)。次要结局指标包括自我报告的OA症状(如疼痛、僵硬和疲劳)、患者对疾病活动的整体评估、测量的手部功能(如握力、拇指蹼间隙和手部灵活性)以及健康相关生活质量。将进行成本效用和成本效益分析。
本研究将有助于了解运动计划对手部OA患者自我报告的手部活动表现进行电话随访的效果和资源使用情况。
该试验已在ClinicalTrials.gov注册,注册号为:NCT01245842。