Population Health Sciences, Addison House, King's College London, Guy's Campus, London, UK.
School of Health Science, University of Nottingham, QMC, Nottingham, UK.
Health Technol Assess. 2024 Oct;28(58):1-141. doi: 10.3310/ADWP8001.
Speech impairments are common with Parkinson's disease (reported prevalence 68%), increasing conversational demands, reliance on family and social withdrawal.
OBJECTIVE(S): The PD COMM trial compared the clinical and cost-effectiveness of two speech and language therapy approaches: Lee Silverman Voice Treatment LOUD and National Health Service speech and language therapy for the treatment of speech or voice problems in people with Parkinson's disease to no speech and language therapy (control) and against each other.
PD COMM is a phase III, multicentre, three-arm, unblinded, randomised controlled trial. Participants were randomised in a 1 : 1 : 1 ratio to control, National Health Service speech and language therapy or Lee Silverman Voice Treatment LOUD via a central computer-generated programme, using a minimisation procedure with a random element, to ensure allocation concealment. Mixed-methods process and health economic evaluations were conducted.
United Kingdom outpatient and home settings.
People with idiopathic Parkinson's disease, with self-reported or carer-reported speech or voice problems. We excluded people with dementia, laryngeal pathology and those within 24 months of previous speech and language therapy.
The Lee Silverman Voice Treatment LOUD intervention included maximum effort drills and high-effort speech production tasks delivered over four 50-minute therapist-led personalised sessions per week, for 4 weeks with prescribed daily home practice. National Health Service speech and language therapy content and dosage reflected local non-Lee Silverman Voice Treatment speech and language therapy practices, usually 1 hour, once weekly, for 6 weeks. Trained, experienced speech and language therapists or assistants provided interventions. The control was no speech and language therapy until the trial was completed.
Primary outcome: Voice Handicap Index total score at 3 months. Secondary outcomes: Voice Handicap Index subscales, Parkinson's Disease Questionnaire-39; Questionnaire on Acquired Speech Disorders; EuroQol-5D-5L; ICEpop Capabilities Measure for Older Adults; Parkinson's Disease Questionnaire - Carers; resource utilisation; and adverse events. Assessments were completed pre-randomisation and at 3, 6 and 12 months post randomisation.
Three hundred and eighty-eight participants were randomised to Lee Silverman Voice Treatment LOUD ( = 130), National Health Service speech and language therapy ( = 129) and control ( = 129). The impact of voice problems at 3 months after randomisation was lower for Lee Silverman Voice Treatment LOUD participants than control [-8.0 (99% confidence interval: -13.3, -2.6); = 0.001]. There was no evidence of improvement for those with access to National Health Service speech and language therapy when compared to control [1.7 (99% confidence interval: -3.8, 7.1); = 0.4]. Participants randomised to Lee Silverman Voice Treatment LOUD reported a lower impact of their voice problems than participants randomised to National Health Service speech and language therapy [99% confidence interval: -9.6 (-14.9, -4.4); < 0.0001]. There were no reports of serious adverse events. Staff were confident with the trial interventions; a range of patient and therapist enablers of implementing Lee Silverman Voice Treatment LOUD were identified. The economic evaluation results suggested Lee Silverman Voice Treatment LOUD was more expensive and more effective than control or National Health Service speech and language therapy but was not cost-effective with incremental cost-effectiveness ratios of £197,772 per quality-adjusted life-year gained and £77,017 per quality-adjusted life-year gained, respectively.
The number of participants recruited to the trial did not meet the pre-specified power.
People that had access to Lee Silverman Voice Treatment LOUD described a significantly greater reduction in the impact of their Parkinson's disease-related speech problems 3 months after randomisation compared to people that had no speech and language therapy. There was no evidence of a difference between National Health Service speech and language therapy and those that received no speech and language therapy. Lee Silverman Voice Treatment LOUD resulted in a significantly lower impact of voice problems compared to National Health Service speech and language therapy 3 months after randomisation which was still present after 12 months; however, Lee Silverman Voice Treatment LOUD was not found to be cost-effective.
Implementing Lee Silverman Voice Treatment LOUD in the National Health Service and identifying alternatives to Lee Silverman Voice Treatment LOUD for those who cannot tolerate it. Investigation of less costly alternative options for Lee Silverman Voice Treatment delivery require investigation, with economic evaluation using a preference-based outcome measure that captures improvement in communication.
This study is registered as ISRCTN12421382.
This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR award ref: 10/135/02) and is published in full in ; Vol. 28, No. 58. See the NIHR Funding and Awards website for further award information.
帕金森病患者常伴有言语障碍(报道的患病率为 68%),这增加了会话需求,依赖于家庭和社交退缩。
PD COMM 试验比较了两种言语治疗方法的临床和成本效益:Lee Silverman 嗓音治疗 LOUD 和英国国家医疗服务体系(NHS)言语治疗,用于治疗帕金森病患者的言语或语音问题,与不进行言语和语言治疗(对照组)以及彼此进行治疗。
PD COMM 是一项 III 期、多中心、三臂、非盲、随机对照试验。参与者以 1:1:1 的比例随机分配至对照组、NHS 言语治疗或 Lee Silverman 嗓音治疗 LOUD,通过中央计算机生成的程序,使用带有随机元素的最小化程序,以确保分配的隐蔽性。进行了混合方法过程和健康经济评估。
英国门诊和家庭环境。
有特发性帕金森病的患者,有自我报告或照料者报告的言语或语音问题。我们排除了有痴呆、喉病理学和那些在过去 24 个月内接受过言语和语言治疗的患者。
Lee Silverman 嗓音治疗 LOUD 干预包括最大努力训练和高强度言语产生任务,每周由一名经过培训的治疗师进行四次,每次 50 分钟,个性化治疗,每周一次,共 6 周,同时还规定了每天的家庭练习。NHS 言语治疗的内容和剂量反映了当地非 Lee Silverman 嗓音治疗的言语治疗实践,通常为 1 小时,每周一次,持续 6 周。经验丰富的言语和语言治疗师或助理提供干预措施。在试验完成之前,对照组不进行言语和语言治疗。
3 个月时的嗓音障碍指数总评分。次要结局指标:嗓音障碍指数子量表、帕金森病问卷-39、获得性言语障碍问卷、EuroQol-5D-5L、老年人能力测试量表、帕金森病问卷-照料者、资源利用情况和不良事件。在随机分组前和随机分组后 3、6 和 12 个月进行评估。
388 名参与者被随机分配至 Lee Silverman 嗓音治疗 LOUD(n=130)、NHS 言语治疗(n=129)和对照组(n=129)。与对照组相比,Lee Silverman 嗓音治疗 LOUD 组参与者在随机分组后 3 个月时的嗓音问题影响较小[-8.0(99%置信区间:-13.3,-2.6);P=0.001]。与对照组相比,接受 NHS 言语治疗的参与者没有改善的证据[1.7(99%置信区间:-3.8,7.1);P=0.4]。与接受 NHS 言语治疗的参与者相比,随机分配至 Lee Silverman 嗓音治疗 LOUD 的参与者报告其嗓音问题的影响较小[99%置信区间:-9.6(-14.9,-4.4);P<0.0001]。没有报告严重不良事件。工作人员对试验干预措施有信心;确定了一系列患者和治疗师的促进因素,以实施 Lee Silverman 嗓音治疗 LOUD。经济评估结果表明,Lee Silverman 嗓音治疗 LOUD 比对照组或 NHS 言语治疗更昂贵,更有效,但增量成本效益比分别为每获得 1 个质量调整生命年增加 197722 英镑和 77017 英镑,因此不具有成本效益。
招募到试验中的参与者人数没有达到预先规定的效力。
与没有言语和语言治疗的参与者相比,接受 Lee Silverman 嗓音治疗 LOUD 的参与者在随机分组后 3 个月时描述了他们帕金森病相关言语问题的影响显著降低。与接受 NHS 言语治疗的参与者相比,没有证据表明 Lee Silverman 嗓音治疗 LOUD 和对照组之间存在差异。与接受 NHS 言语治疗的参与者相比,Lee Silverman 嗓音治疗 LOUD 组在随机分组后 3 个月时的嗓音问题影响显著降低,且在 12 个月后仍存在;然而,Lee Silverman 嗓音治疗 LOUD 并不具有成本效益。
在英国国家医疗服务体系中实施 Lee Silverman 嗓音治疗 LOUD,并为不能耐受 Lee Silverman 嗓音治疗 LOUD 的患者寻找替代方法。需要研究成本较低的替代 Lee Silverman 嗓音治疗 LOUD 方案,并使用捕捉沟通改善的偏好性结果测量方法进行经济评估。
本研究已在英国临床试验注册库(ISRCTN84641145)注册。
该奖项由英国国家卫生与保健研究院(NIHR)健康技术评估计划(NIHR 奖号:10/135/02)资助,并全文发表在;第 28 卷,第 58 期。欲了解更多关于该奖项的信息,请访问 NIHR 资助和奖项网站。