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Identifying spatial neglect - an updated systematic review of the psychometric properties of assessment tools in adults post-stroke. 识别空间忽略--中风后成人评估工具心理测量特性的最新系统回顾。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-04-01 Epub Date: 2024-05-10 DOI: 10.1080/09602011.2024.2346212
Lindy J Williams, Tobias Loetscher, Susan Hillier, Kimberly Hreha, Jennifer Jones, Audrey Bowen, Jocelyn Kernot

Spatial neglect commonly occurs after a stroke, resulting in diverse impacts depending on the type and severity. There are almost 300 tools for assessing neglect, yet there is a lack of knowledge on the psychometric properties of these tools. The objective of this systematic review, registered on Prospero (CRD42021271779), was to determine the quality of the evidence for assessing spatial neglect, categorized by neglect subtype. The following databases were searched on 3rd May 2022 from database inception: Ovid Emcare, Embase, Ovid MEDLINE, APA PsycINFO, Web of Science (SCI-EXPANDED; SSCI; A&HCI; ESCI) and Scopus. All primary peer-reviewed studies (>5 participants) of adults post stroke, reporting any psychometric property of 33 commonly used neglect assessment tools were included. The COSMIN (COnsensus-based Standards for the selection of health Measurement INstruments) risk of bias tool was used to assess the methodological quality of the studies and summarize the psychometric properties of each tool. 164 articles were included, with a total of 12,463 people with stroke. The general quality of the evidence was poor and no one tool had high-quality evidence of both validity and reliability. Eleven tools show some promise as they meet the minimum criteria for good measurement properties for both validity and reliability.

空间忽略通常发生在中风后,根据类型和严重程度的不同会造成不同的影响。目前有近 300 种评估忽视的工具,但人们对这些工具的心理测量特性缺乏了解。本系统性综述已在 Prospero(CRD42021271779)上注册,目的是确定按忽视亚型分类的空间忽视评估证据的质量。从 2022 年 5 月 3 日开始,对以下数据库进行了检索:Ovid Emcare、Embase、Ovid MEDLINE、APA PsycINFO、Web of Science(SCI-EXPANDED;SSCI;A&HCI;ESCI)和 Scopus。纳入了所有针对中风后成人、报告了 33 种常用忽视评估工具任何心理测量特性的主要同行评审研究(参与人数大于 5 人)。采用 COSMIN(基于共识的健康测量工具选择标准)偏倚风险工具评估研究的方法学质量,并总结每种工具的心理测量特性。共纳入 164 篇文章,涉及 12,463 名中风患者。证据的总体质量较差,没有一种工具同时具有高质量的有效性和可靠性证据。有 11 种工具在有效性和可靠性方面都达到了良好测量特性的最低标准,显示出一定的前景。
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引用次数: 0
Assessment of executive function impairments in adults with acquired brain injury across single-case experimental design: A scoping review of primary outcomes. 通过单例实验设计评估后天性脑损伤成人的执行功能障碍:主要结果的范围综述。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-04-01 Epub Date: 2024-05-13 DOI: 10.1080/09602011.2024.2345410
C Lebely, E Lepron, C Villepinte, S Scannella, X De Boissezon

The use of single-case experimental design (SCED) to evaluate cognitive remediation is growing. SCEDs require rigorous methodology and appropriate choice of primary outcomes. To review primary outcomes that assess executive function impairments in patients with acquired brain injury (ABI). A scoping review was conducted using the Arksey and O'Malley framework and the PRISMA extension for scoping review (PRISMA-ScR). Five databases were searched resulting in the inclusion of twenty-one studies. Primary outcomes were extracted and classified according to the type of measure, ecological setting and sources of possible bias. A wide variety of primary outcomes were identified; the majority of which evaluated behavioural performance during a real-life activity or in a real-life simulated setting. The most frequent bias observed across outcomes was the coaching effect. The findings of this scoping review highlight the importance of selecting appropriate outcomes for repeated measures in SCED studies. Direct observation of the target behaviour is a potential gold standard for assessing the effectiveness of a cognitive intervention.

使用单例实验设计(SCED)来评估认知矫正的情况越来越多。单病例实验设计需要严格的方法论和适当的主要结果选择。对评估后天性脑损伤(ABI)患者执行功能障碍的主要结果进行回顾。采用 Arksey 和 O'Malley 框架以及用于范围界定审查的 PRISMA 扩展(PRISMA-ScR)进行了范围界定审查。对五个数据库进行了检索,最终纳入了 21 项研究。根据测量类型、生态环境和可能的偏差来源,对主要结果进行了提取和分类。研究发现了各种各样的主要结果,其中大部分都是对真实活动或真实模拟环境中的行为表现进行评估。在各种结果中最常见的偏差是教练效应。本次范围界定审查的结果凸显了在 SCED 研究中为重复测量选择适当结果的重要性。对目标行为的直接观察是评估认知干预有效性的潜在黄金标准。
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引用次数: 0
Comparing the Oxford Digital Multiple Errands Test (OxMET) to a real-life version: Convergence, feasibility, and acceptability. 牛津数字多重任务测试(OxMET)与现实生活版本的比较:收敛性、可行性和可接受性。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-04-01 Epub Date: 2024-05-11 DOI: 10.1080/09602011.2024.2344326
Sam S Webb, Nele Demeyere

We aimed to assess the convergence, feasibility, and acceptability of the Oxford Digital Multiple Errands Test (OxMET) and the in-person Multiple Errands Test-Home version (MET-Home). Participants completed OxMET, MET-Home, Montreal Cognitive Assessment (MoCA), and questionnaires on activities of daily living, depression, technology usage, mobility, and disability. Forty-eight stroke survivors (mean age 69.61, 41.67% female, and average 16.5 months post-stroke) and 50 controls (mean age 71.46, 56.00% female) took part. No performance differences were found for healthy and stroke participants for MET-Home, and only found below p = .05 for OxMET but not below the corrected p = .006. Convergent validity was found between MET-Home and OxMET metrics (most r ≥ .30, p < .006). MET-Home accuracy was related to age (B = -.04, p = .03), sex (B = -.98, p = .03), disability (B = -0.63, p = .04), and MoCA (B = .26, p < .001), whereas OxMET accuracy was predicted by MoCA score (B = .40, p < .001). Feedback indicated that the OxMET was easy and fun and more acceptable than the MET-Home. The MET-Home was more stressful and interesting. The MET tasks demonstrated good convergent validity, with the OxMET digital administration providing a more feasible, inclusive, and acceptable assessment, especially to people with mobility restrictions and more severe stroke.

我们的目的是评估牛津数字多重任务测试(OxMET)和个人多重任务测试-家庭版(MET-Home)的趋同性、可行性和可接受性。参与者完成了 OxMET、MET-Home、蒙特利尔认知评估(MoCA)以及有关日常生活活动、抑郁、技术使用、行动能力和残疾的问卷调查。48 名中风幸存者(平均年龄 69.61 岁,女性占 41.67%,平均中风后 16.5 个月)和 50 名对照组(平均年龄 71.46 岁,女性占 56.00%)参加了此次活动。在 MET-Home 中,健康参与者和中风参与者的表现没有差异;在 OxMET 中,只有低于 p = 0.05 的差异,但没有低于校正后的 p = 0.006 的差异。在 MET-Home 和 OxMET 指标(最 r ≥ .30,p p = .03)、性别(B = -.98,p = .03)、残疾(B = -0.63,p = .04)和 MoCA(B = .26,p B = .40,p B = .05)之间发现了收敛有效性。
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引用次数: 0
Null cross-modal effects of olfactory training on visual, auditory or olfactory working memory in 6- to 9-year-old children. 嗅觉训练对 6 至 9 岁儿童的视觉、听觉或嗅觉工作记忆的跨模态效应为零。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-04-01 Epub Date: 2024-05-19 DOI: 10.1080/09602011.2024.2343484
Michal Pieniak, Marta Rokosz, Paulina Nawrocka, Aleksandra Reichert, Barbara Zyzelewicz, Mehmet K Mahmut, Anna Oleszkiewicz

Systematic exposure to odours (olfactory training, OT) is a method of smell loss treatment. Due to olfactory system projections to prefrontal brain areas, OT has been hypothesized to enhance cognitive functions, but its effects have been studied predominantly in adults. This study tested OT effects on working memory (WM), i.e., the ability to store and manipulate information for a short time, in healthy children aged 6-9 years. We expected OT to improve olfactory WM and establish cross-modal transfer to visual and auditory WM. Participants performed 12 weeks of bi-daily OT with either 4 odours (lemon, eucalyptus, rose, cloves; OT group) or odourless propylene glycol (placebo group). Pre- and post-training, participants' WM was measured utilizing odours (olfactory WM) or pictures (visual WM) and a word-span task (auditory WM). 84 children (40 girls) completed the study. The analyses revealed no changes in the WM performance following OT. The olfactory WM task was the most difficult for children, highlighting the need to include olfactory-related tasks in educational programmes to improve children's odour knowledge and memory, just as they learn about sounds and pictures. Further neuroimaging research is needed to fully understand the impact of OT on cognitive functions in children.

系统性接触气味(嗅觉训练,OT)是治疗嗅觉缺失的一种方法。由于嗅觉系统投射到大脑前额叶区域,因此人们假定嗅觉训练能增强认知功能,但其效果主要是在成人身上进行研究的。本研究测试了 OT 对 6-9 岁健康儿童工作记忆(WM)的影响,即短时间储存和处理信息的能力。我们期望加时训练能改善嗅觉工作记忆,并建立向视觉和听觉工作记忆的跨模态转移。参与者进行了为期 12 周的双日 OT 训练,训练内容为 4 种气味(柠檬、桉树、玫瑰、丁香;OT 组)或无味丙二醇(安慰剂组)。在训练前和训练后,利用气味(嗅觉 WM)或图片(视觉 WM)和单词跨度任务(听觉 WM)测量参与者的 WM。84 名儿童(40 名女孩)完成了这项研究。分析表明,加时训练后的 WM 表现没有变化。嗅觉 WM 任务对儿童来说是最难的,这说明有必要在教育计划中加入与嗅觉相关的任务,以提高儿童的气味知识和记忆力,就像他们学习声音和图片一样。要全面了解定向行走对儿童认知功能的影响,还需要进一步的神经影像学研究。
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引用次数: 0
A pilot rating system to evaluate the quality of goal attainment scales used as outcome measures in rehabilitation. 试点评级系统,用于评估作为康复成果衡量标准的目标实现量表的质量。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-04-01 Epub Date: 2024-05-28 DOI: 10.1080/09602011.2024.2343150
Charles Pradeau, Severine Estival, Virginie Postal, Virginie Laurier, Céline Maugard, Marie-Eve Isner-Horobeti, Fabien Mourre, Agata Krasny-Pacini

Goal Attainment Scaling (GAS) is a method for writing person-centred approach evaluation scales that can be used as an outcome measure in clinical or research settings in rehabilitation. To be used in a research setting, it requires a high methodological quality approach. The aim of this study was to explore the feasibility and reliability of the GAS quality rating system, to ensure that GAS scales used as outcome measures are valid and reliable. Secondary objectives were: (1) to compare goal attainment scores' reliability according to how many GAS levels are described in the scale; and (2) to explore if GAS scorings are influenced by who scores goal attainment. The GAS scales analysed here were set collaboratively by 57 cognitively impaired adults clients and their occupational therapist. Goals had to be achieved within an inpatient one-month stay, during which clients participated in an intervention aimed at improving planning skills in daily life. The GAS quality rating system proved to be feasible and reliable. Regarding GAS scores, interrater reliability was higher when only three of the five GAS levels were described, i.e., "three milestone GAS" (0.74-0.92), than when all five levels were described (0.5-0.88), especially when scored by the clients (0.5 -0.88).

目标达成量表(GAS)是一种编写以人为本的评估量表的方法,可用作康复临床或研究环境中的结果测量。要在研究环境中使用,它需要高方法质量的方法。本研究旨在探索 GAS 质量评级系统的可行性和可靠性,以确保用作结果测量的 GAS 量表有效可靠。次要目标是(1) 根据量表中描述的 GAS 等级的多少,比较目标达成得分的可靠性;(2) 探讨 GAS 评分是否受目标达成评分者的影响。本文分析的 GAS 量表是由 57 名认知障碍成人客户及其职业治疗师共同制定的。目标必须在住院一个月的时间内实现,在此期间,患者参加了旨在提高日常生活规划能力的干预活动。事实证明,GAS 质量评分系统是可行且可靠的。在 GAS 评分方面,如果只描述 GAS 五个等级中的三个等级,即 "三个里程碑 GAS"(0.74-0.92),则相互之间的可靠性要高于描述所有五个等级(0.5-0.88)时的可靠性,尤其是由客户评分时(0.5-0.88)。
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引用次数: 0
Goal management training for improving fatigue in children and adolescents with acquired brain injuries: A 2-year follow-up of a randomised controlled trial. 改善后天性脑损伤儿童和青少年疲劳状况的目标管理训练:随机对照试验的两年随访。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-04-01 Epub Date: 2024-06-07 DOI: 10.1080/09602011.2024.2353395
Hanna Lovise Sargénius, Ruth Elizabeth Hypher, Torun Gangaune Finnanger, Anne Elisabeth Brandt, Stein Andersson, Kari Risnes, Torstein Baade Rø, Jan Egil Stubberud

To explore the long-term effectiveness of a paediatric adaptation of Goal Management Training (pGMT), relative to a psychoeducative program (pBHW), in reducing fatigue after pABI 2 years post-intervention. Thirty-eight youths and their parents completed the Paediatric Quality of Life - Multidimensional Fatigue Scale. Primary outcome measures were Total Fatigue Score, General fatigue, Cognitive fatigue, and Sleep/rest fatigue (parent-report). No significant differences in fatigue symptoms by the parental report was observed between the intervention groups at the 2-year follow-up (total score: F = .16, p = .69; general fatigue: F = .36, p = .55; sleep/rest: F = .48, p = .49; and cognitive fatigue: F = .09, p = .76), nor any time*group interactions (total score: F = .25, p = .86; general fatigue: F = .39, p = .76; sleep/rest: F = .20, p = .89; and cognitive fatigue: F = .08, p = .97). In total, 45% of the participants in the pGMT group and 25% in the pBHW group demonstrated a reliable positive clinical change. The significant improvements in fatigue symptoms that were demonstrated 6 months post-intervention could not be confirmed in this 2-year follow-up study. However, a continued positive tendency on most dimensions of fatigue for the participants in the pGMT group could be observed, suggesting that cognitive rehabilitation may help reduce fatigue.

目的:探讨儿科目标管理训练(pGMT)与心理教育计划(pBHW)相比,在减少儿童脑损伤干预两年后的疲劳方面的长期有效性。38 名青少年及其家长完成了儿科生活质量多维疲劳量表。主要结果指标包括疲劳总分、一般疲劳、认知疲劳和睡眠/休息疲劳(家长报告)。在为期两年的随访中,根据家长的报告,干预组之间的疲劳症状无明显差异(总分:F = .16,p = .0):F = .16,p = .69;一般疲劳:F = .36,p = .55;睡眠/休息:F = .48,p = .49;认知疲劳:F = .09,p = .76),也没有任何时间*组间的交互作用(总分:总分:F = .25,p = .86;一般疲劳:F = .39,p = .86:F = .39,p = .76;睡眠/休息:F = .20,p = .89;认知疲劳:F = .08,p = .97)。总共有 45% 的 pGMT 组参与者和 25% 的 pBHW 组参与者表现出了可靠的积极临床变化。干预后 6 个月疲劳症状的明显改善在为期 2 年的随访研究中未能得到证实。不过,可以观察到 pGMT 组的参与者在疲劳的大多数维度上都有持续的积极趋势,这表明认知康复可能有助于减轻疲劳。
{"title":"Goal management training for improving fatigue in children and adolescents with acquired brain injuries: A 2-year follow-up of a randomised controlled trial.","authors":"Hanna Lovise Sargénius, Ruth Elizabeth Hypher, Torun Gangaune Finnanger, Anne Elisabeth Brandt, Stein Andersson, Kari Risnes, Torstein Baade Rø, Jan Egil Stubberud","doi":"10.1080/09602011.2024.2353395","DOIUrl":"10.1080/09602011.2024.2353395","url":null,"abstract":"<p><p>To explore the long-term effectiveness of a paediatric adaptation of Goal Management Training (pGMT), relative to a psychoeducative program (pBHW), in reducing fatigue after pABI 2 years post-intervention. Thirty-eight youths and their parents completed the Paediatric Quality of Life - Multidimensional Fatigue Scale. Primary outcome measures were Total Fatigue Score, General fatigue, Cognitive fatigue, and Sleep/rest fatigue (parent-report). No significant differences in fatigue symptoms by the parental report was observed between the intervention groups at the 2-year follow-up (total score: <i>F </i>= .16, <i>p</i> = .69; general fatigue: <i>F </i>= .36, <i>p</i> = .55; sleep/rest: <i>F </i>= .48, <i>p</i> = .49; and cognitive fatigue: <i>F </i>= .09, <i>p</i> = .76), nor any time*group interactions (total score: <i>F </i>= .25, <i>p</i> = .86; general fatigue: <i>F </i>= .39, <i>p</i> = .76; sleep/rest: <i>F </i>= .20, <i>p</i> = .89; and cognitive fatigue: <i>F </i>= .08, <i>p</i> = .97). In total, 45% of the participants in the pGMT group and 25% in the pBHW group demonstrated a reliable positive clinical change. The significant improvements in fatigue symptoms that were demonstrated 6 months post-intervention could not be confirmed in this 2-year follow-up study. However, a continued positive tendency on most dimensions of fatigue for the participants in the pGMT group could be observed, suggesting that cognitive rehabilitation may help reduce fatigue.</p>","PeriodicalId":54729,"journal":{"name":"Neuropsychological Rehabilitation","volume":" ","pages":"572-592"},"PeriodicalIF":1.7,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141288947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluating the VaLiANT (Valued Living After Neurological Trauma) group intervention for improving adjustment to life with acquired brain injury: A pilot randomized controlled trial.
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-03-18 DOI: 10.1080/09602011.2025.2476074
Nick Sathananthan, Eric M J Morris, Roshan das Nair, David Gillanders, Bradley Wright, Dana Wong

There is a need for accessible rehabilitation that promotes meaningful participation, wellbeing, and adjustment to life with acquired brain injury (ABI). VaLiANT (Valued Living After Neurological Trauma) is an 8-week holistic group intervention that integrates Acceptance and Commitment Therapy (ACT) and cognitive rehabilitation techniques to support adjustment and meaningful reengagement in life. This Phase II pilot randomized controlled trial explored feasibility and preliminary efficacy signals to determine the viability of a larger trial. Adults (>3 months post-ABI) were randomly allocated to VaLiANT plus treatment-as-usual (TAU), or TAU waitlist-control, with assessments at baseline, post-intervention (8 weeks), and follow-up (16 weeks). Feasibility criteria included recruitment, dropout, outcome assessment completion, adherence, and delivery fidelity. Preliminary treatment effects were assessed on a range of adjustment-related outcomes using mixed linear models, proportions of reliable change, and minimal clinically important differences. 54 participants were recruited (Mage = 50.6, Myears-post-injury = 5.4) predominately with stroke (52%) and traumatic brain injury (22%). All feasibility criteria were met. Treatment effects were identified on measures of psychological distress, experiential avoidance, valued living, and self-identity, but not meaningful participation, quality-of-life, or wellbeing. A larger trial is viable but VaLiANT will benefit from refinement first to improve its impact on all intended outcomes.Trial registration: ACTRN12619001243101.

{"title":"Evaluating the VaLiANT (Valued Living After Neurological Trauma) group intervention for improving adjustment to life with acquired brain injury: A pilot randomized controlled trial.","authors":"Nick Sathananthan, Eric M J Morris, Roshan das Nair, David Gillanders, Bradley Wright, Dana Wong","doi":"10.1080/09602011.2025.2476074","DOIUrl":"https://doi.org/10.1080/09602011.2025.2476074","url":null,"abstract":"<p><p>There is a need for accessible rehabilitation that promotes meaningful participation, wellbeing, and adjustment to life with acquired brain injury (ABI). VaLiANT (Valued Living After Neurological Trauma) is an 8-week holistic group intervention that integrates Acceptance and Commitment Therapy (ACT) and cognitive rehabilitation techniques to support adjustment and meaningful reengagement in life. This Phase II pilot randomized controlled trial explored feasibility and preliminary efficacy signals to determine the viability of a larger trial. Adults (>3 months post-ABI) were randomly allocated to VaLiANT plus treatment-as-usual (TAU), or TAU waitlist-control, with assessments at baseline, post-intervention (8 weeks), and follow-up (16 weeks). Feasibility criteria included recruitment, dropout, outcome assessment completion, adherence, and delivery fidelity. Preliminary treatment effects were assessed on a range of adjustment-related outcomes using mixed linear models, proportions of reliable change, and minimal clinically important differences. 54 participants were recruited (<i>M</i><sub>age </sub>= 50.6, <i>M</i><sub>years-post-injury</sub> = 5.4) predominately with stroke (52%) and traumatic brain injury (22%). All feasibility criteria were met. Treatment effects were identified on measures of psychological distress, experiential avoidance, valued living, and self-identity, but not meaningful participation, quality-of-life, or wellbeing. A larger trial is viable but VaLiANT will benefit from refinement first to improve its impact on all intended outcomes.<b>Trial registration:</b> ACTRN12619001243101.</p>","PeriodicalId":54729,"journal":{"name":"Neuropsychological Rehabilitation","volume":" ","pages":"1-29"},"PeriodicalIF":1.7,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143659646","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Auditory motion stimulation as an add-on therapeutical approach is feasible, enjoyable, and associated with a significant improvement of neglect outcome: A non-randomized, controlled group-matched study. 听觉运动刺激作为一种附加治疗方法是可行的、令人愉悦的,并能显著改善忽视结果:一项非随机、对照组匹配研究。
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-03-14 DOI: 10.1080/09602011.2025.2476068
Nora Geiser, Brigitte C Kaufmann, Dario Cazzoli, Tobias Nef, Thomas Nyffeler

Auditory motion stimulation is a promising new therapeutical approach for visual neglect, whereby patients listen to music which repeatedly moves from the ipsi - to the contralateral hemispace. In this study, we investigated the feasibility, enjoyability, and efficacy of auditory motion simulation in an inpatient neurorehabilitation setting. 30 patients with left-sided visual neglect due to a right-hemispheric subacute stroke participated in the study. 15 patients were included prospectively and received 45 minutes of auditory motion stimulation per day for three weeks in addition to best possible standard neglect therapy. 15 further patients - who were matched based on neglect severity at admission, time since stroke, rehabilitation duration, and age - received best possible standard neglect therapy alone and served as a control group. Feasibility was assessed using remote time tracking, whereas enjoyability was measured with the Flow State Scale for Rehabilitation Tasks (FSSRT). Efficacy was evaluated using video-oculography during free visual exploration (FVE) at admission, discharge, and after three months. Our findings indicate that auditory motion stimulation is feasible and enjoyed by patients. Auditory motion stimulation significantly improved visual neglect at discharge. Randomized controlled studies are needed to confirm that auditory motion stimulation represents a valuable add-on therapy for visual neglect.

{"title":"Auditory motion stimulation as an add-on therapeutical approach is feasible, enjoyable, and associated with a significant improvement of neglect outcome: A non-randomized, controlled group-matched study.","authors":"Nora Geiser, Brigitte C Kaufmann, Dario Cazzoli, Tobias Nef, Thomas Nyffeler","doi":"10.1080/09602011.2025.2476068","DOIUrl":"https://doi.org/10.1080/09602011.2025.2476068","url":null,"abstract":"<p><p>Auditory motion stimulation is a promising new therapeutical approach for visual neglect, whereby patients listen to music which repeatedly moves from the ipsi - to the contralateral hemispace. In this study, we investigated the feasibility, enjoyability, and efficacy of auditory motion simulation in an inpatient neurorehabilitation setting. 30 patients with left-sided visual neglect due to a right-hemispheric subacute stroke participated in the study. 15 patients were included prospectively and received 45 minutes of auditory motion stimulation per day for three weeks in addition to best possible standard neglect therapy. 15 further patients - who were matched based on neglect severity at admission, time since stroke, rehabilitation duration, and age - received best possible standard neglect therapy alone and served as a control group. Feasibility was assessed using remote time tracking, whereas enjoyability was measured with the Flow State Scale for Rehabilitation Tasks (FSSRT). Efficacy was evaluated using video-oculography during free visual exploration (FVE) at admission, discharge, and after three months. Our findings indicate that auditory motion stimulation is feasible and enjoyed by patients. Auditory motion stimulation significantly improved visual neglect at discharge. Randomized controlled studies are needed to confirm that auditory motion stimulation represents a valuable add-on therapy for visual neglect.</p>","PeriodicalId":54729,"journal":{"name":"Neuropsychological Rehabilitation","volume":" ","pages":"1-15"},"PeriodicalIF":1.7,"publicationDate":"2025-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143631064","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An online, group Acceptance and Commitment Therapy is acceptable to stroke survivors: A qualitative interview study.
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-03-10 DOI: 10.1080/09602011.2025.2469649
Hannah Foote, Audrey Bowen, Sarah Cotterill, Emma Patchwood

Mental health difficulties are common post-stroke and developing support for psychological adjustment is a research priority. Wellbeing After Stroke (WAterS) is a nine-week, online, group-based Acceptance and Commitment Therapy (ACT)-informed intervention, delivered by trained third-sector practitioners, supervised by a clinical neuropsychologist. This study aimed to explore the acceptability of WAterS from the stroke survivors' perspective.Semi-structured interviews were conducted with twelve stroke survivors who received WAterS. The interview schedule was informed by theorised components of acceptability, including understanding, burden and perception of effectiveness. The data were analysed inductively and deductively using Template Analysis.Six qualitative themes were generated. Results indicate the intervention was mostly understandable and participants were able to engage with ACT and apply it to life. Online delivery reduced burden in accessing the intervention, and was acceptable when supported by live facilitation and a physical handbook. Group cohesion and understanding was facilitated by practitioners. The social aspect of the group was beneficial. Attending WAterS supported some participants to seek further support; others were left feeling unsupported when the intervention ended.Stroke survivors valued attending an online, group ACT-informed intervention, delivered by practitioners. This is a promising avenue in increasing the reach of interventions to support wellbeing.

{"title":"An online, group Acceptance and Commitment Therapy is acceptable to stroke survivors: A qualitative interview study.","authors":"Hannah Foote, Audrey Bowen, Sarah Cotterill, Emma Patchwood","doi":"10.1080/09602011.2025.2469649","DOIUrl":"https://doi.org/10.1080/09602011.2025.2469649","url":null,"abstract":"<p><p>Mental health difficulties are common post-stroke and developing support for psychological adjustment is a research priority. Wellbeing After Stroke (WAterS) is a nine-week, online, group-based Acceptance and Commitment Therapy (ACT)-informed intervention, delivered by trained third-sector practitioners, supervised by a clinical neuropsychologist. This study aimed to explore the acceptability of WAterS from the stroke survivors' perspective.Semi-structured interviews were conducted with twelve stroke survivors who received WAterS. The interview schedule was informed by theorised components of acceptability, including understanding, burden and perception of effectiveness. The data were analysed inductively and deductively using Template Analysis.Six qualitative themes were generated. Results indicate the intervention was mostly understandable and participants were able to engage with ACT and apply it to life. Online delivery reduced burden in accessing the intervention, and was acceptable when supported by live facilitation and a physical handbook. Group cohesion and understanding was facilitated by practitioners. The social aspect of the group was beneficial. Attending WAterS supported some participants to seek further support; others were left feeling unsupported when the intervention ended.Stroke survivors valued attending an online, group ACT-informed intervention, delivered by practitioners. This is a promising avenue in increasing the reach of interventions to support wellbeing.</p>","PeriodicalId":54729,"journal":{"name":"Neuropsychological Rehabilitation","volume":" ","pages":"1-19"},"PeriodicalIF":1.7,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143598379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Eye movement desensitization and reprocessing for posttraumatic stress disorder following acquired brain injury: A multiple baseline single case experimental design study across four cases.
IF 1.7 3区 心理学 Q4 NEUROSCIENCES Pub Date : 2025-03-04 DOI: 10.1080/09602011.2024.2444999
Ellen P J Janssen, Peggy J J Spauwen, Sophie J M Rijnen, Rudolf W H M Ponds

Posttraumatic stress disorder (PTSD) is prevalent in individuals with acquired brain injury (ABI). This study investigated the effectiveness and applicability of Eye Movement Desensitization and Reprocessing (EMDR) for PTSD in individuals with ABI. Data were collected using a non-concurrent multiple baseline single case experimental design (SCED), with a baseline, treatment, maintenance, and 3-month follow-up phase, across four cases. EMDR treatment was provided using a manualized standard EMDR protocol. The primary outcome was PTSD symptoms. Secondary outcomes were general mental health and cognitive functions. Visual analyses, TAU-U analyses, and analyses using the Reliable Change Index were performed. All four participants (two with TBI, two with stroke) showed a significant decrease in PTSD symptoms, which continued in maintenance and was retained at follow-up. The participants no longer fulfilled criteria for PTSD classification and showed reliable improvement in PTSD severity score post-treatment and at follow-up. No adverse events occurred and no adjustments in EMDR protocol were necessary. There was no consistent improvement in general mental health nor a consistent improvement in cognitive functioning. This study provided empirical support for the effectiveness and applicability of EMDR for PTSD in four participants with stroke or TBI.

{"title":"Eye movement desensitization and reprocessing for posttraumatic stress disorder following acquired brain injury: A multiple baseline single case experimental design study across four cases.","authors":"Ellen P J Janssen, Peggy J J Spauwen, Sophie J M Rijnen, Rudolf W H M Ponds","doi":"10.1080/09602011.2024.2444999","DOIUrl":"10.1080/09602011.2024.2444999","url":null,"abstract":"<p><p>Posttraumatic stress disorder (PTSD) is prevalent in individuals with acquired brain injury (ABI). This study investigated the effectiveness and applicability of Eye Movement Desensitization and Reprocessing (EMDR) for PTSD in individuals with ABI. Data were collected using a non-concurrent multiple baseline single case experimental design (SCED), with a baseline, treatment, maintenance, and 3-month follow-up phase, across four cases. EMDR treatment was provided using a manualized standard EMDR protocol. The primary outcome was PTSD symptoms. Secondary outcomes were general mental health and cognitive functions. Visual analyses, TAU-<i>U</i> analyses, and analyses using the Reliable Change Index were performed. All four participants (two with TBI, two with stroke) showed a significant decrease in PTSD symptoms, which continued in maintenance and was retained at follow-up. The participants no longer fulfilled criteria for PTSD classification and showed reliable improvement in PTSD severity score post-treatment and at follow-up. No adverse events occurred and no adjustments in EMDR protocol were necessary. There was no consistent improvement in general mental health nor a consistent improvement in cognitive functioning. This study provided empirical support for the effectiveness and applicability of EMDR for PTSD in four participants with stroke or TBI.</p>","PeriodicalId":54729,"journal":{"name":"Neuropsychological Rehabilitation","volume":" ","pages":"1-29"},"PeriodicalIF":1.7,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143558607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Neuropsychological Rehabilitation
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