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职业疗法优化帕金森病患者独立性的试点随机对照试验:帕金森病职业疗法试验(PD OT试验)

Pilot randomised controlled trial of occupational therapy to optimise independence in Parkinson's disease: the PD OT trial.

作者信息

Clarke C E, Furmston A, Morgan E, Patel S, Sackley C, Walker M, Bryan S, Wheatley K

机构信息

Department of Neurology, City Hospital, Dudley Road, Birmingham B18 7QH, UK.

出版信息

J Neurol Neurosurg Psychiatry. 2009 Sep;80(9):976-8. doi: 10.1136/jnnp.2007.138586. Epub 2008 Mar 13.

Abstract

OBJECTIVE

To perform a pilot trial of occupational therapy (OT) to optimise functional independence in Parkinson disease (PD) to assess accrual/withdrawal rates, acceptability, outcome measures, and inform sample-size calculation.

METHOD

Non-demented patients with idiopathic PD and difficulties with activities of daily living (ADL) were recruited provided they had not received OT in the last 2 years and/or physiotherapy in the last year. Patients were randomised to immediate OT or OT after completion of the trial. Patients randomised to OT were assessed at home by an experienced therapist and then received six home treatment sessions over 2 months. Interventions were targeted at functional independence and mobility goals. Outcome measures were: Nottingham Extended Activity of Daily Living Scale, Rivermead Mobility Index, Unified Parkinson's Disease Rating Scale ADL scale, Parkinson's Disease Questionnaire 39, EuroQol-EQ-5D, Hospital Anxiety and Depression Scale, and health economics analysis.

RESULTS

39 patients (25 male; mean age 73 years) were recruited from four centres over 16 months. The mean difference in NEADL at 8 months was 3.5 (95% CI -3.2 to 10.2). The mean difference in PDQ-39 Summary Score was 3.8 (95% CI -4.94 to 12.6). There were strong correlations between the PDQ-39 and other outcomes. The intervention was acceptable to patients, with a low withdrawal rate and good questionnaire completion.

CONCLUSION

Randomisation to a trial of OT in PD is feasible. NEADL and PDQ-39 are relevant outcomes and provided data to inform sample size for an adequately powered randomised trial for which there is pressing need.

摘要

目的

开展一项职业治疗(OT)的试点试验,以优化帕金森病(PD)患者的功能独立性,评估入组/退出率、可接受性、结局指标,并为样本量计算提供依据。

方法

招募无痴呆的特发性PD患者且日常生活活动(ADL)有困难,条件是他们在过去2年未接受过OT和/或在过去1年未接受过物理治疗。患者被随机分为立即接受OT组或试验完成后接受OT组。随机分配至OT组的患者由经验丰富的治疗师在家中进行评估,然后在2个月内接受6次家庭治疗课程。干预措施针对功能独立性和活动能力目标。结局指标包括:诺丁汉扩展日常生活活动量表、里弗米德活动能力指数、统一帕金森病评定量表ADL量表、帕金森病问卷39项、欧洲五维度健康量表(EQ-5D)、医院焦虑抑郁量表以及卫生经济学分析。

结果

在16个月内从4个中心招募了39名患者(25名男性;平均年龄73岁)。8个月时诺丁汉扩展日常生活活动量表的平均差异为3.5(95%可信区间-3.2至10.2)。帕金森病问卷39项总分的平均差异为3.8(95%可信区间-4.94至12.6)。帕金森病问卷39项与其他结局之间存在强相关性。该干预措施患者可接受,退出率低且问卷完成情况良好。

结论

将PD患者随机分配至OT试验是可行的。诺丁汉扩展日常生活活动量表和帕金森病问卷39项是相关结局指标,并为有迫切需求的充分有力的随机试验提供了样本量计算的数据。

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