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首页> 外文期刊>Pilot and Feasibility Studies >Lee Silverman Voice Treatment versus standard speech and language therapy versus control in Parkinson’s disease: a pilot randomised controlled trial (PD COMM pilot)
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Lee Silverman Voice Treatment versus standard speech and language therapy versus control in Parkinson’s disease: a pilot randomised controlled trial (PD COMM pilot)

机译:Lee Silverman语音治疗与标准言语和语言疗法与帕金森氏病对照:一项随机对照试验(PD COMM飞行员)

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摘要

Speech-related problems are common in Parkinson’s disease (PD), but there is little evidence for the effectiveness of standard speech and language therapy (SLT) or Lee Silverman Voice Treatment (LSVT LOUD?).MethodsThe PD COMM pilot was a three-arm, assessor-blinded, randomised controlled trial (RCT) of LSVT LOUD?, SLT and no intervention (1:1:1 ratio) to assess the feasibility and to inform the design of a full-scale RCT. Non-demented patients with idiopathic PD and speech problems and no SLT for speech problems in the past 2?years were eligible. LSVT LOUD? is a standardised regime (16 sessions over 4?weeks). SLT comprised individualised content per local practice (typically weekly sessions for 6–8?weeks). Outcomes included recruitment and retention, treatment adherence, and data completeness. Outcome data collected at baseline, 3, 6, and 12?months included patient-reported voice and quality of life measures, resource use, and assessor-rated speech recordings.ResultsEighty-nine patients were randomised with 90% in the therapy groups and 100% in the control group completing the trial. The response rate for Voice Handicap Index (VHI) in each arm was ≥?90% at all time-points. VHI was highly correlated with the other speech-related outcome measures. There was a trend to improvement in VHI with LSVT LOUD? (difference at 3?months compared with control: ??12.5 points; 95% CI ??26.2, 1.2) and SLT (difference at 3?months compared with control: ??9.8 points; 95% CI ??23.2, 3.7) which needs to be confirmed in an adequately powered trial.ConclusionRandomisation to a three-arm trial of speech therapy including a no intervention control is feasible and acceptable. Compliance with both interventions was good. VHI and other patient-reported outcomes were relevant measures and provided data to inform the sample size for a substantive trial.Trial registrationInternational Standard Randomised Controlled Trial Number Register: ISRCTN75223808. registered 22 March 2012.
机译:与语音相关的问题在帕金森氏病(PD)中很常见,但很少有证据表明标准语音和语言疗法(SLT)或李·西尔弗曼语音治疗(LSVT LOUD?)的有效性。 ,评估者盲法,LSVT LOUD?,SLT的随机对照试验(RCT),无需干预(1:1:1的比例),以评估可行性并为全面的RCT设计提供依据。过去2年中患有特发性PD和言语问题且无SLT言语问题的无痴呆患者符合条件。 LSVT大声?是一种标准化的治疗方案(4个星期内进行16个疗程)。 SLT包含每个本地实践的个性化内容(通常为6-8周的每周课程)。结果包括招募和保留,治疗依从性和数据完整性。在基线,3、6和12个月时收集的结果数据包括患者报告的语音和生活质量测评,资源使用情况以及评估者评定的语音记录。结果89例患者被随机分为治疗组和对照组,分别为90%和100%完成试验的对照组中的百分比。在所有时间点,每个手臂的语音障碍指数(VHI)响应率均≥90%。 VHI与其他与言语相关的结局指标高度相关。 LSVT LOUD有改善VHI的趋势吗? (与对照组相比3个月时的差异:12.5点; 95%CI 26.2、1.2)和SLT(与对照组相比3个月时的差异:9.8点; 95%CI 23.2,3.7)结论随机化到三臂语音治疗试验中,包括无干预控制是可行且可以接受的。两种干预措施的依从性均良好。 VHI和其他患者报告的结局是相关措施,并提供了数据来告知实质性试验的样本量。试验注册国际标准随机对照试验注册号:ISRCTN75223808。于2012年3月22日注册。

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