运动神经元疾病患者行为症状管理在线干预(MiNDToolkit):随机平行多中心可行性试验。

E Mioshi, K Grant, E Flanagan, S Heal, H Copsey, R L Gould, M Hammond, L Shepstone, P A Ashford
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引用次数: 0

摘要

背景:有关运动神经元疾病(MND)行为症状管理的证据尚缺。MiNDToolkit是一个在线心理教育平台,为照顾者处理行为症状(BehSymp)提供支持。研究目标是确定招募率和保留率、照护者和医疗保健专业人员 (HCP) 对该平台的使用情况以及在线评估的完成情况,为全面试验提供依据。设计:随机、平行、多中心、可行性试验:英格兰和威尔士,不同的 MND 服务机构;21 年 7 月至 22 年 11 月招募;23 年 3 月对最后一名参与者进行随访:通过 MND 服务机构招募的患有 BehSymp 的运动神经元病患者 (PwMND) 的照顾者。在确认资格后,参与者通过 MiNDToolkit 平台在线完成筛查和基线评估,并按 1:1 的比例随机分配到 MiNDToolkit 或对照组:在为期 3 个月的研究期间,MiNDToolkit 为照护者提供量身定制的模块。干预组的照护者可以从接受过 MiNDToolkit 培训的保健人员那里获得额外的支持。对照组则在研究结束时接受干预。研究收集了有关平台使用情况和社会心理变量的数据:来自 11 个地点的 151 名照护者受邀参加研究(信函、面对面);30 人通过筛选;29 人被随机分配。15人被分配到对照组;14人被分配到干预组。照顾者大多为女性;年龄中位数为 62.5 岁(IQR:58,68;干预组)和 57 岁(IQR:56,70;对照组)。研究保留率很高(24/29 = 82.76%);在研究期间,照护者平均使用平台 14 次(中位数(IQR):14.0 (10.0, 18.5)):结论:MiNDToolkit 研究是可行的,并得到了照护者和经过培训的保健医生的认可。有必要进行最终试验。
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An online intervention for carers to manage behavioral symptoms in motor neuron disease (MiNDToolkit): a randomized parallel multi-center feasibility trial.

Background: Evidence on management of behavioral symptoms in motor neuron disease (MND) is lacking. The MiNDToolkit, an online psychoeducational platform, supports carers dealing with behavioral symptoms (BehSymp). The study objectives were to ascertain recruitment and retention rates, carer and healthcare professional (HCP) use of the platform, and completion of online assessments, to inform a full-scale trial. Design: Randomized, parallel, multi-center, feasibility trial.

Setting: England and Wales, across diverse MND services; recruitment from July/21 to November/22; last participant follow-up in March/23.

Participants: Carers of people with motor neuron disease (PwMND) with BehSymp, recruited through MND services. After confirming eligibility, participants completed screening and baseline assessments online via the MiNDToolkit platform and were randomized centrally in a 1:1 ratio to MiNDToolkit or control.

Intervention: MiNDToolkit offered tailored modules to carers for the 3-month study period. Carers in the intervention group could receive additional support from MiNDToolkit trained HCPs. The control group was offered access to the intervention at the end of the study. Data were collected on platform usage and psychosocial variables.

Main outcomes: One hundred and fifty-one carers from 11 sites were invited to join the study (letter, face-to-face); 30 were screened; 29 were randomized. Fifteen people were allocated to the control arm; 14 to intervention. Carers were mostly female; median age for was 62.5 (IQR: 58, 68; intervention) and 57 (IQR: 56, 70; controls). Study retention was high (24/29 = 82.76%); carers engaged with the platform on average 14 times (median (IQR):14.0 (10.0, 18.5)) during the study period.

Conclusion: The MiNDToolkit study was feasible and well accepted by carers and trained HCPs. A definitive trial is warranted.

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