Pub Date : 2025-11-01Epub Date: 2025-09-15DOI: 10.1177/02692155251376622
Fadi M Al Zoubi, Arnold Yl Wong, Mandy Mp Kan, Aliki Thomas, André E Bussières
ObjectiveTo explore the perspectives and experiences of patients with knee osteoarthritis regarding physiotherapy care management in Hong Kong.DesignQualitative study using semi-structured, individual interviews.SettingCommunity.ParticipantsPatients age 50 years or older with knee osteoarthritis, purposively recruited.InterventionFace-to-face semi-structured interviews were conducted with patients who had completed a physiotherapy rehabilitation programme in the past six months.Main MeasuresA 21-question interview guide encouraged participants to discuss their physiotherapy management, experiences, and recommended interventions, covering all non-pharmacological treatments outlined in local clinical guidelines. Questions also explored factors influencing adherence to care during and after physiotherapy. Interviews were audio-recorded, transcribed verbatim, and analysed thematically.ResultsFourteen patients participated. Five key themes emerged: (a) navigating pain and management strategies; (b) adapting daily life and the impact of knee osteoarthritis on activities; (c) complexities of treatment and the need for personalised care; (d) the role of exercise and mobility; and (e) barriers to access and resources. While patients reported receiving various physiotherapy interventions, gaps were noted in aquatic therapy, neuromuscular training, weight management, and assistive devices. Barriers included limited access, financial constraints, and lack of home exercise equipment. Although participants valued physical activity, maintaining an exercise routine was challenging.ConclusionsA comprehensive, patient-centred approach is essential for effective physiotherapy care for knee osteoarthritis in Hong Kong. Addressing practical barriers and integrating patient feedback can enhance the accessibility and impact of evidence-based interventions.
{"title":"Patients' perspectives and experiences on physiotherapy care for knee osteoarthritis: A qualitative study.","authors":"Fadi M Al Zoubi, Arnold Yl Wong, Mandy Mp Kan, Aliki Thomas, André E Bussières","doi":"10.1177/02692155251376622","DOIUrl":"10.1177/02692155251376622","url":null,"abstract":"<p><p>ObjectiveTo explore the perspectives and experiences of patients with knee osteoarthritis regarding physiotherapy care management in Hong Kong.DesignQualitative study using semi-structured, individual interviews.SettingCommunity.ParticipantsPatients age 50 years or older with knee osteoarthritis, purposively recruited.InterventionFace-to-face semi-structured interviews were conducted with patients who had completed a physiotherapy rehabilitation programme in the past six months.Main MeasuresA 21-question interview guide encouraged participants to discuss their physiotherapy management, experiences, and recommended interventions, covering all non-pharmacological treatments outlined in local clinical guidelines. Questions also explored factors influencing adherence to care during and after physiotherapy. Interviews were audio-recorded, transcribed verbatim, and analysed thematically.ResultsFourteen patients participated. Five key themes emerged: (a) navigating pain and management strategies; (b) adapting daily life and the impact of knee osteoarthritis on activities; (c) complexities of treatment and the need for personalised care; (d) the role of exercise and mobility; and (e) barriers to access and resources. While patients reported receiving various physiotherapy interventions, gaps were noted in aquatic therapy, neuromuscular training, weight management, and assistive devices. Barriers included limited access, financial constraints, and lack of home exercise equipment. Although participants valued physical activity, maintaining an exercise routine was challenging.ConclusionsA comprehensive, patient-centred approach is essential for effective physiotherapy care for knee osteoarthritis in Hong Kong. Addressing practical barriers and integrating patient feedback can enhance the accessibility and impact of evidence-based interventions.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1467-1491"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145069245","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-02DOI: 10.1177/02692155251371435
Hatem Lazem, David Harris, Abi Hall, Maedeh Mansoubi, Rodrigo Garcia Pontes, Carlos Bandeira de Mello Monteiro, Luciano Vieira de Araújo, Sarah E Lamb, Helen Dawes
ObjectiveThis study adopted a novel approach to exploring the content validity, safety, usability, and user experiences of different games for telerehabilitation purposes from the perspective of physiotherapists and stroke survivors.DesignA cross-sectional content validity and usability study.SettingLab and online.Participants23 participants were recruited; 11 neuro-physiotherapists and 12 chronic stroke survivors.OutcomesContent validity and safety were assessed using a bespoke state evaluation questionnaire. The usability was evaluated using the system usability scale (SUS) and user experience questionnaire (UEQ). House of Quality analysis was conducted to identify the priority aspects for improvement.ResultsPhysiotherapists perceived the usability of the games as good to excellent for three games, median SUS = 80%, and poor for two games SUS < 68%. Three games had a mean average content validity index (CVI) > 0.8, and all games were safe to be administrated at home; mean CVI-safety item = 0.90. Stroke survivors with Fugl-Meyer Assessment of Upper Extremity function mean (SD) = 41(19.4), and mild to moderate spasticity perceived usability as very good to excellent for four games (median SUS = 85%). UEQ scale showed good to excellent acceptance among most of the games. House of Quality analysis revealed that clear instructions, avatar quality, motivational exercise scenarios, and clinical assessment tools are important criteria that should be considered throughout the development.ConclusionThis study demonstrated the value of exploring patient and physiotherapist perspectives for better telerehabilitation interventions co-development. Clinical trials should be conducted after further refinement of the games to investigate their feasibility and potential efficacy as a telerehabilitation tool for arm and balance training.
目的以物理治疗师和脑卒中幸存者为研究对象,探讨不同远程康复游戏的内容效度、安全性、可用性和用户体验。设计一个横断面的内容效度和可用性研究。SettingLab和在线。参与者:招募了23名参与者;11名神经物理治疗师和12名慢性中风幸存者。结果:使用定制的状态评估问卷评估内容的有效性和安全性。采用系统可用性量表(SUS)和用户体验问卷(UEQ)对系统的可用性进行评价。进行了质量之家分析,以确定需要改进的优先方面。结果物理治疗师对游戏易用性的评价为:3个游戏的易用性为好至优,SUS中位数为80%,2个游戏的易用性较差,SUS为0.8,所有游戏均可安全在家使用;平均cvi -安全项目= 0.90。Fugl-Meyer上肢功能评估的中风幸存者平均(SD) = 41(19.4),轻度至中度痉挛的患者在4个游戏中认为可用性非常好到优秀(SUS中位数= 85%)。UEQ量表在大多数游戏中表现出良好到优秀的接受度。House of Quality分析显示,明确的指导、虚拟角色的质量、动机练习场景和临床评估工具是整个开发过程中应该考虑的重要标准。结论本研究显示了探索患者和物理治疗师的观点对更好的远程康复干预共同开发的价值。在进一步完善游戏后,应进行临床试验,以研究其作为手臂和平衡训练远程康复工具的可行性和潜在功效。
{"title":"Validity, safety, usability, and user experience of virtual reality gamified home-based exercises in stroke.","authors":"Hatem Lazem, David Harris, Abi Hall, Maedeh Mansoubi, Rodrigo Garcia Pontes, Carlos Bandeira de Mello Monteiro, Luciano Vieira de Araújo, Sarah E Lamb, Helen Dawes","doi":"10.1177/02692155251371435","DOIUrl":"10.1177/02692155251371435","url":null,"abstract":"<p><p>ObjectiveThis study adopted a novel approach to exploring the content validity, safety, usability, and user experiences of different games for telerehabilitation purposes from the perspective of physiotherapists and stroke survivors.DesignA cross-sectional content validity and usability study.SettingLab and online.Participants23 participants were recruited; 11 neuro-physiotherapists and 12 chronic stroke survivors.OutcomesContent validity and safety were assessed using a bespoke state evaluation questionnaire. The usability was evaluated using the system usability scale (SUS) and user experience questionnaire (UEQ). House of Quality analysis was conducted to identify the priority aspects for improvement.ResultsPhysiotherapists perceived the usability of the games as good to excellent for three games, median SUS = 80%, and poor for two games SUS < 68%. Three games had a mean average content validity index (CVI) > 0.8, and all games were safe to be administrated at home; mean CVI-safety item = 0.90. Stroke survivors with Fugl-Meyer Assessment of Upper Extremity function mean (SD) = 41(19.4), and mild to moderate spasticity perceived usability as very good to excellent for four games (median SUS = 85%). UEQ scale showed good to excellent acceptance among most of the games. House of Quality analysis revealed that clear instructions, avatar quality, motivational exercise scenarios, and clinical assessment tools are important criteria that should be considered throughout the development.ConclusionThis study demonstrated the value of exploring patient and physiotherapist perspectives for better telerehabilitation interventions co-development. Clinical trials should be conducted after further refinement of the games to investigate their feasibility and potential efficacy as a telerehabilitation tool for arm and balance training.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1527-1540"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12521778/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144945092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-09DOI: 10.1177/02692155251375369
Bianca A Ramos, Kavita Ram, Maylyn Martinez, Aashna Sunderrajan, Jacob Sindorf, Megan K O'Brien, Sara Prokup, Sehar Siddiqui, Linda L Morris, Kristen L Knutson, Babak Mokhlesi, Shyam Prabhakaran, Lisa F Wolfe, Phyllis C Zee, Arun Jayaraman, Vineet M Arora
ObjectiveTo adapt and modify the successful SIESTA (Sleep for Inpatients: Empowering Staff to Act) sleep-promoting hospital protocol to an acute stroke rehabilitation setting.DesignThis study utilized a mixed methods design, involving qualitative surveys and interviews. Needs assessment and staff interviews informed the development of the adapted protocol, SIESTA-Rehab.SettingInpatient unit treating persons with neurological injury, primarily stroke, in an acute rehabilitation hospital.ParticipantsNursing staff on the inpatient unit where SIESTA-Rehab was implemented.InterventionAfter identifying needs, we adapted the SIESTA protocol with relevant modifications to SIESTA-Rehab. Protocol adaptations were guided by the Culture, Oversight, Systems Change, Training framework, with a focus on developing nursing education and sleep-enhancing tools. The protocol was implemented over a four-year period, sustained through periodic staff re-education, and nursing staff perceptions of the intervention were evaluated using fidelity interviews.Main MeasuresQualitative assessments were conducted from a convenience sample of nurses to gauge understanding, recall, ease of implementation, and individual re-education needs for SIESTA-Rehab.ResultsInitial staff feedback indicated limited awareness of sleep disorder screening and sleep optimization practices, highlighting the absence of sleep-based assessments during standard care. Initial unit-wide training was conducted on SIESTA-Rehab for nursing staff (N = 29), with ongoing education for new staff and periodic re-education for existing staff over 4 years of implementation. Fidelity interviews revealed high understanding, recall, and ease of implementing the intervention over survey periods.ConclusionsSIESTA-Rehab can be successfully implemented in an acute rehabilitation setting, as indicated through positive staff responses.
{"title":"Adapting and implementing a staff-led sleep intervention in an acute rehabilitation setting.","authors":"Bianca A Ramos, Kavita Ram, Maylyn Martinez, Aashna Sunderrajan, Jacob Sindorf, Megan K O'Brien, Sara Prokup, Sehar Siddiqui, Linda L Morris, Kristen L Knutson, Babak Mokhlesi, Shyam Prabhakaran, Lisa F Wolfe, Phyllis C Zee, Arun Jayaraman, Vineet M Arora","doi":"10.1177/02692155251375369","DOIUrl":"10.1177/02692155251375369","url":null,"abstract":"<p><p>ObjectiveTo adapt and modify the successful SIESTA (Sleep for Inpatients: Empowering Staff to Act) sleep-promoting hospital protocol to an acute stroke rehabilitation setting.DesignThis study utilized a mixed methods design, involving qualitative surveys and interviews. Needs assessment and staff interviews informed the development of the adapted protocol, SIESTA-Rehab.SettingInpatient unit treating persons with neurological injury, primarily stroke, in an acute rehabilitation hospital.ParticipantsNursing staff on the inpatient unit where SIESTA-Rehab was implemented.InterventionAfter identifying needs, we adapted the SIESTA protocol with relevant modifications to SIESTA-Rehab. Protocol adaptations were guided by the Culture, Oversight, Systems Change, Training framework, with a focus on developing nursing education and sleep-enhancing tools. The protocol was implemented over a four-year period, sustained through periodic staff re-education, and nursing staff perceptions of the intervention were evaluated using fidelity interviews.Main MeasuresQualitative assessments were conducted from a convenience sample of nurses to gauge understanding, recall, ease of implementation, and individual re-education needs for SIESTA-Rehab.ResultsInitial staff feedback indicated limited awareness of sleep disorder screening and sleep optimization practices, highlighting the absence of sleep-based assessments during standard care. Initial unit-wide training was conducted on SIESTA-Rehab for nursing staff (<i>N</i> = 29), with ongoing education for new staff and periodic re-education for existing staff over 4 years of implementation. Fidelity interviews revealed high understanding, recall, and ease of implementing the intervention over survey periods.ConclusionsSIESTA-Rehab can be successfully implemented in an acute rehabilitation setting, as indicated through positive staff responses.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1492-1503"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145029022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
ObjectiveThis systematic review and meta-analysis aimed to evaluate the effects of cervical lateral glide and median nerve neural mobilisation compared to no treatment and other physical therapy treatments on pain, function and disability in patients with nerve-related neck and arm pain.Data sourcesElectronic searches were conducted in MEDLINE, Science Direct, Cochrane Library, PEDro and Google Scholar up to 30 June 2025.Review methodsRandomised controlled trials were included following PRISMA guidelines. Two authors independently selected relevant studies, extracted data, assessed risk of bias (RoB2 tool), and rated evidence quality. Meta-analysis was performed using random-effects models due to expected heterogeneity. The study was registered on PROSPERO (CRD42020216739).ResultsOverall, 20 studies with 953 patients met the inclusion criteria. Cervical lateral glide reduced pain compared to no treatment (3 studies, MD -2.47; 95%CI: -3.41, -1.53; P < .001) and other physical therapy techniques (2 studies, MD -1.29; 95%CI: -2.54, -0.05; P = .04). Median nerve neural mobilisation also reduced pain compared to no treatment (4 studies, MD -3.07; 95%CI: -3.78, -2.37; P < .001). Both interventions had modest effects on disability (12 studies, SMD -0.50 to -1.22), with moderate-to-high heterogeneity in analyses. The certainty of evidence was low to very low.ConclusionCervical lateral glide and median nerve neural mobilisation are clinically effective for reducing nerve-related neck and arm pain as part of multimodal management strategies. The quality of evidence remains low as the level of certainty. Targeting a population with a clear nociceptive, increased neural mechanosensitivity or neuropathic component should lead to better clinical outcomes.
目的:本系统综述和荟萃分析旨在评估颈椎外侧滑动和正中神经活动对神经相关性颈臂疼痛患者疼痛、功能和残疾的影响,与不治疗和其他物理治疗相比。数据来源截止到2025年6月30日,在MEDLINE、Science Direct、Cochrane Library、PEDro和谷歌Scholar进行了电子检索。回顾方法随机对照试验纳入PRISMA指南。两位作者独立选择相关研究,提取数据,评估偏倚风险(RoB2工具),并评价证据质量。由于预期的异质性,采用随机效应模型进行meta分析。该研究已在PROSPERO注册(CRD42020216739)。结果共有20项研究953例患者符合纳入标准。与未治疗相比,颈椎侧滑减轻了疼痛(3项研究,MD -2.47; 95%CI: -3.41, -1.53; P = 0.04)。与未治疗相比,正中神经活动也减轻了疼痛(4项研究,MD -3.07; 95%CI: -3.78, -2.37; P
{"title":"Effect of median nerve neural mobilisation and cervical lateral glide on pain, disability and function in patients with nerve-related neck and arm pain: A systematic review and meta-analysis.","authors":"Timothée Gillot, Damien Lefebvre, Alexis Michalak, Léa Miossec, Yann Combret, Grégoire Prum","doi":"10.1177/02692155251370881","DOIUrl":"10.1177/02692155251370881","url":null,"abstract":"<p><p>ObjectiveThis systematic review and meta-analysis aimed to evaluate the effects of cervical lateral glide and median nerve neural mobilisation compared to no treatment and other physical therapy treatments on pain, function and disability in patients with nerve-related neck and arm pain.Data sourcesElectronic searches were conducted in MEDLINE, Science Direct, Cochrane Library, PEDro and Google Scholar up to 30 June 2025.Review methodsRandomised controlled trials were included following PRISMA guidelines. Two authors independently selected relevant studies, extracted data, assessed risk of bias (RoB2 tool), and rated evidence quality. Meta-analysis was performed using random-effects models due to expected heterogeneity. The study was registered on PROSPERO (CRD42020216739).ResultsOverall, 20 studies with 953 patients met the inclusion criteria. Cervical lateral glide reduced pain compared to no treatment (3 studies, MD -2.47; 95%CI: -3.41, -1.53; <i>P</i> < .001) and other physical therapy techniques (2 studies, MD -1.29; 95%CI: -2.54, -0.05; <i>P</i> = .04). Median nerve neural mobilisation also reduced pain compared to no treatment (4 studies, MD -3.07; 95%CI: -3.78, -2.37; <i>P</i> < .001). Both interventions had modest effects on disability (12 studies, SMD -0.50 to -1.22), with moderate-to-high heterogeneity in analyses. The certainty of evidence was low to very low.ConclusionCervical lateral glide and median nerve neural mobilisation are clinically effective for reducing nerve-related neck and arm pain as part of multimodal management strategies. The quality of evidence remains low as the level of certainty. Targeting a population with a clear nociceptive, increased neural mechanosensitivity or neuropathic component should lead to better clinical outcomes.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1405-1424"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145084638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-24DOI: 10.1177/02692155251375382
Nathan Johns, Dean McKenzie, Bernadette Brady, Justine Naylor, John Olver
ObjectiveModerate to severe persistent pain can affect up to 25% of people after a knee replacement for osteoarthritis. The aim of the trial was to test the feasibility of implementing Kneed, a novel digital pain rehabilitation self-management programme.DesignProspective, two group parallel randomised pilot study.SettingOnline in Australia.ParticipantsAdults with persistent pain rated as ≥4/10 in the operated knee more than 3 months post-knee replacement for osteoarthritis.InterventionThe Kneed group were provided with 8 weeks of access to a digital pain rehabilitation self-management programme and compared to usual care.Main measuresRecruitment, acceptability, usability and limited efficacy with descriptive statistics.ResultsSixty participants, mean age 68.7 years, 75% female, 66.7% retired and 43% living outside metropolitan areas, were recruited between 15 October and 19 December, 2024 via social media advertising with 418 online eligibility surveys performed. There were 190 (45.5%) deemed potentially eligible; 82 (19.6%) left contact details and 60 (14.4%) consented. At 8 weeks, there were 48 (80%) participants remaining in the trial (20 Kneed (64.5%), 28 usual care (96.6%)). A majority of the Kneed group found the Kneed programme acceptable, would use it again and found that it helped them effectively manage pain and function.ConclusionIt is feasible to recruit and retain older Australians with moderate to severe knee pain post-knee replacement for a trial testing a digital pain rehabilitation self-management programme. A larger trial is indicated to further test the clinical effectiveness of Kneed to reduce pain and improve function.
{"title":"A pilot randomised controlled trial of an online self-management programme for people with persistent pain post-knee replacement (Kneed).","authors":"Nathan Johns, Dean McKenzie, Bernadette Brady, Justine Naylor, John Olver","doi":"10.1177/02692155251375382","DOIUrl":"10.1177/02692155251375382","url":null,"abstract":"<p><p>ObjectiveModerate to severe persistent pain can affect up to 25% of people after a knee replacement for osteoarthritis. The aim of the trial was to test the feasibility of implementing Kneed, a novel digital pain rehabilitation self-management programme.DesignProspective, two group parallel randomised pilot study.SettingOnline in Australia.ParticipantsAdults with persistent pain rated as ≥4/10 in the operated knee more than 3 months post-knee replacement for osteoarthritis.InterventionThe Kneed group were provided with 8 weeks of access to a digital pain rehabilitation self-management programme and compared to usual care.Main measuresRecruitment, acceptability, usability and limited efficacy with descriptive statistics.ResultsSixty participants, mean age 68.7 years, 75% female, 66.7% retired and 43% living outside metropolitan areas, were recruited between 15 October and 19 December, 2024 via social media advertising with 418 online eligibility surveys performed. There were 190 (45.5%) deemed potentially eligible; 82 (19.6%) left contact details and 60 (14.4%) consented. At 8 weeks, there were 48 (80%) participants remaining in the trial (20 Kneed (64.5%), 28 usual care (96.6%)). A majority of the Kneed group found the Kneed programme acceptable, would use it again and found that it helped them effectively manage pain and function.ConclusionIt is feasible to recruit and retain older Australians with moderate to severe knee pain post-knee replacement for a trial testing a digital pain rehabilitation self-management programme. A larger trial is indicated to further test the clinical effectiveness of Kneed to reduce pain and improve function.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1438-1451"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12521762/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145130206","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-12DOI: 10.1177/02692155251374575
Gemma Foley, Rose Galvin, Frances Horgan
ObjectiveTo explore the attitudes and practice of allied health professionals working in stroke care in Ireland regarding recommended amounts of therapy set out in the National Clinical Guideline for Stroke (2023).DesignQualitative descriptive study using one-to-one semi-structured interviews. Data were analysed using reflexive thematic analysis.SettingFive large acute teaching hospitals in Dublin, Ireland.ParticipantsThe 11 participants were allied health professionals working in acute and subacute stroke care in Dublin, and were recruited using a combination of purposive and snowball sampling.ResultsTwo main themes emerged: 'Barriers and enablers to achieving guideline recommended therapy time' and 'Methods of increasing therapeutic time'. Patient factors and clinical resources impact on the provision of therapy post-stroke. Overall, participants felt positive about the recent guideline recommendation for increased therapeutic time. Various methods are employed to augment patient therapeutic time, including technology and semi-supervised practice. Participants perceived that Therapy Assistants play an important role in achieving greater amounts of therapy.ConclusionsAllied health professionals view the new Stroke Guidelines recommendation for increased therapy intensity as challenging but are generally positive in trying to achieve it, citing the benefits of increased therapy time for patient outcomes. They utilise a wide range of methods to optimise therapeutic time for stroke survivors. The role of the therapy assistant in supporting the delivery of larger amounts of therapy time warrants further evaluation.
{"title":"Exploring allied health professionals' perceptions and practice in Ireland regarding guideline recommendations for intensity of multidisciplinary therapy for stroke survivors: A qualitative study.","authors":"Gemma Foley, Rose Galvin, Frances Horgan","doi":"10.1177/02692155251374575","DOIUrl":"10.1177/02692155251374575","url":null,"abstract":"<p><p>ObjectiveTo explore the attitudes and practice of allied health professionals working in stroke care in Ireland regarding recommended amounts of therapy set out in the National Clinical Guideline for Stroke (2023).DesignQualitative descriptive study using one-to-one semi-structured interviews. Data were analysed using reflexive thematic analysis.SettingFive large acute teaching hospitals in Dublin, Ireland.ParticipantsThe 11 participants were allied health professionals working in acute and subacute stroke care in Dublin, and were recruited using a combination of purposive and snowball sampling.ResultsTwo main themes emerged: 'Barriers and enablers to achieving guideline recommended therapy time' and 'Methods of increasing therapeutic time'. Patient factors and clinical resources impact on the provision of therapy post-stroke. Overall, participants felt positive about the recent guideline recommendation for increased therapeutic time. Various methods are employed to augment patient therapeutic time, including technology and semi-supervised practice. Participants perceived that Therapy Assistants play an important role in achieving greater amounts of therapy.ConclusionsAllied health professionals view the new Stroke Guidelines recommendation for increased therapy intensity as challenging but are generally positive in trying to achieve it, citing the benefits of increased therapy time for patient outcomes. They utilise a wide range of methods to optimise therapeutic time for stroke survivors. The role of the therapy assistant in supporting the delivery of larger amounts of therapy time warrants further evaluation.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1504-1514"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145039271","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-23DOI: 10.1177/02692155251372114
Anne-Fleur Domensino, Johanna Ma Visser-Meily, Jacoba M Spikman, Caroline van Heugten
ObjectiveEvaluate the internal consistency, inter-rater and test-retest reliability, convergent and divergent validity and clinical usability of the Cognition in Daily Life scale for patients with acquired brain injury.DesignValidation study.ParticipantsA total of 75 patients with acquired brain injury (mostly male [n = 47, 68%]; mean age 67 years) were recruited from inpatient care facilities. Sixty participants (81%) had sustained a stroke.Main measuresOutcome measure: Cognition in Daily Life scale. Reference measures: Utrecht Scale for Rehabilitation-Cognition subscale, Montreal Cognitive Assessment, Barthel Index, Hospital Anxiety and Depression Scale and Fatigue Severity Scale.ResultsAfter removing redundant items, all subscales of the Cognition in Daily Life scale demonstrated satisfactory internal consistency. Test-retest reliability was good (intraclass correlation coefficient [ICC] = 0.847), and inter-rater reliability was moderate (ICC = 0.615). Convergent validity was confirmed through moderately strong correlations between most subscales of the Cognition in Daily Life Scale and other measures of cognition. Cognition in Daily Life subscales generally did not correlate with the Hospital Anxiety and Depression Scale and Fatigue Severity Scale, indicating divergent validity. Moderate correlations with the Barthel Index suggested related, but distinct constructs. Clinicians found the Cognition in Daily Life scale easy to administer and relevant for practice, though time-consuming. They suggested layout improvements for greater usability.ConclusionThe Cognition in Daily Life scale is adequately valid, reliable and clinically usable for assessing cognition in daily life in patients with acquired brain injury in a clinical setting. Future research needs to evaluate the scale's sensitivity to change and its performance in other settings and populations.
{"title":"Psychometric properties and clinical usability of the cognition in daily life scale in patients with acquired brain injury in clinical care settings.","authors":"Anne-Fleur Domensino, Johanna Ma Visser-Meily, Jacoba M Spikman, Caroline van Heugten","doi":"10.1177/02692155251372114","DOIUrl":"10.1177/02692155251372114","url":null,"abstract":"<p><p>ObjectiveEvaluate the internal consistency, inter-rater and test-retest reliability, convergent and divergent validity and clinical usability of the Cognition in Daily Life scale for patients with acquired brain injury.DesignValidation study.ParticipantsA total of 75 patients with acquired brain injury (mostly male [<i>n</i> = 47, 68%]; mean age 67 years) were recruited from inpatient care facilities. Sixty participants (81%) had sustained a stroke.Main measures<i>Outcome measure:</i> Cognition in Daily Life scale. <i>Reference measures:</i> Utrecht Scale for Rehabilitation-Cognition subscale, Montreal Cognitive Assessment, Barthel Index, Hospital Anxiety and Depression Scale and Fatigue Severity Scale.ResultsAfter removing redundant items, all subscales of the Cognition in Daily Life scale demonstrated satisfactory internal consistency. Test-retest reliability was good (intraclass correlation coefficient [ICC] = 0.847), and inter-rater reliability was moderate (ICC = 0.615). Convergent validity was confirmed through moderately strong correlations between most subscales of the Cognition in Daily Life Scale and other measures of cognition. Cognition in Daily Life subscales generally did not correlate with the Hospital Anxiety and Depression Scale and Fatigue Severity Scale, indicating divergent validity. Moderate correlations with the Barthel Index suggested related, but distinct constructs. Clinicians found the Cognition in Daily Life scale easy to administer and relevant for practice, though time-consuming. They suggested layout improvements for greater usability.ConclusionThe Cognition in Daily Life scale is adequately valid, reliable and clinically usable for assessing cognition in daily life in patients with acquired brain injury in a clinical setting. Future research needs to evaluate the scale's sensitivity to change and its performance in other settings and populations.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1452-1466"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145124498","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-16DOI: 10.1177/02692155251378371
Wenming Chu, Xiaoman Deng, Ling Gao, Xiyan Gao
{"title":"Response letter to \"Letter to the editor on a recent paper on acupuncture with pelvic floor rehabilitation training\".","authors":"Wenming Chu, Xiaoman Deng, Ling Gao, Xiyan Gao","doi":"10.1177/02692155251378371","DOIUrl":"10.1177/02692155251378371","url":null,"abstract":"","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1543-1544"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145074341","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-09-05DOI: 10.1177/02692155251374911
Someka Hijikuro, Takao Kaneko, Kohei Ikeda
ObjectiveThis scoping review aimed to comprehensively map interventions for post-stroke apathy and their effects.Data sourcesThe literature search for this review was performed using PubMed, Cumulative Index to Nursing and Allied Health Literature, and Web of Science, targeting studies published until August 7, 2025.Review methodsThis scoping review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for scoping reviews. The population included patients with post-stroke apathy; the concept focused on post-stroke apathy assessment and interventions and their effects. The context covered both general and community healthcare settings. Controlled vocabulary (e.g., MeSH terms) such as "post-stroke apathy," "intervention," and "effect" was used to formulate the search strategy. The eligible studies were independently screened by three reviewers, and final inclusion was determined through discussion.ResultsOf the 565 studies identified, 13 met the inclusion criteria (n = 13). The mapping revealed that pharmacological interventions not only improved and prevented post-stroke apathy symptoms but also alleviated emotional blunting, reduced loss of motivation and interest, and enhanced social behavior and participation. Non-pharmacological interventions were associated with symptom relief and recovery over time. Furthermore, combined pharmacological and non-pharmacological approaches contributed to improvements not only in post-stroke apathy but also in depression, language function, and behavioral aspects.ConclusionThe findings suggest that appropriate treatment for post-stroke apathy may lead to symptom relief, improvement, and prevention while enhancing language function, behavior, and social participation. Future research should focus on systematic reviews and meta-analyses to establish evidence-based recommendations for post-stroke apathy treatment strategies and their optimal combinations.
目的:本综述旨在全面了解脑卒中后冷漠的干预措施及其效果。数据来源本综述的文献检索使用PubMed、护理和相关健康文献累积索引和Web of Science,目标是2025年8月7日之前发表的研究。综述方法:本综述按照系统综述和荟萃分析扩展的首选报告项目进行。人群包括卒中后冷漠患者;该概念侧重于脑卒中后冷漠的评估和干预措施及其效果。背景包括一般和社区卫生保健环境。控制词汇(例如MeSH术语)如“中风后冷漠”、“干预”和“效果”被用来制定搜索策略。符合条件的研究由三位审稿人独立筛选,并通过讨论确定最终纳入。结果纳入的565项研究中,13项符合纳入标准(n = 13)。该图谱显示,药物干预不仅可以改善和预防中风后的冷漠症状,还可以缓解情绪迟钝,减少动机和兴趣的丧失,增强社会行为和参与。随着时间的推移,非药物干预与症状缓解和恢复有关。此外,药物和非药物相结合的方法不仅有助于改善中风后的冷漠,还有助于改善抑郁、语言功能和行为方面。结论适当治疗脑卒中后冷漠可缓解、改善和预防症状,同时提高语言功能、行为和社会参与能力。未来的研究应侧重于系统评价和荟萃分析,以建立卒中后冷漠治疗策略及其最佳组合的循证建议。
{"title":"Interventions for post-stroke apathy and their effects: A scoping review.","authors":"Someka Hijikuro, Takao Kaneko, Kohei Ikeda","doi":"10.1177/02692155251374911","DOIUrl":"10.1177/02692155251374911","url":null,"abstract":"<p><p>ObjectiveThis scoping review aimed to comprehensively map interventions for post-stroke apathy and their effects.Data sourcesThe literature search for this review was performed using PubMed, Cumulative Index to Nursing and Allied Health Literature, and Web of Science, targeting studies published until August 7, 2025.Review methodsThis scoping review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for scoping reviews. The population included patients with post-stroke apathy; the concept focused on post-stroke apathy assessment and interventions and their effects. The context covered both general and community healthcare settings. Controlled vocabulary (e.g., MeSH terms) such as \"post-stroke apathy,\" \"intervention,\" and \"effect\" was used to formulate the search strategy. The eligible studies were independently screened by three reviewers, and final inclusion was determined through discussion.ResultsOf the 565 studies identified, 13 met the inclusion criteria (<i>n</i> = 13). The mapping revealed that pharmacological interventions not only improved and prevented post-stroke apathy symptoms but also alleviated emotional blunting, reduced loss of motivation and interest, and enhanced social behavior and participation. Non-pharmacological interventions were associated with symptom relief and recovery over time. Furthermore, combined pharmacological and non-pharmacological approaches contributed to improvements not only in post-stroke apathy but also in depression, language function, and behavioral aspects.ConclusionThe findings suggest that appropriate treatment for post-stroke apathy may lead to symptom relief, improvement, and prevention while enhancing language function, behavior, and social participation. Future research should focus on systematic reviews and meta-analyses to establish evidence-based recommendations for post-stroke apathy treatment strategies and their optimal combinations.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1425-1437"},"PeriodicalIF":2.9,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144999864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-31DOI: 10.1177/02692155251391669
Annick Van Gils, Yue Zou, Sarah Meyer, Marc Michielsen, Christophe Lafosse, Hilde Beyens, Fabienne Schillebeeckx, Daphne Kos, Geert Verheyden
ObjectiveTo characterize the trajectory and identify early predictors of bimanual performance at 6 and 12 months post-stroke.DesignProspective longitudinal study with assessments at admission, 6, and 12 months post-stroke.SettingInpatient rehabilitation centre.ParticipantsFirst-ever stroke survivors with unilateral upper limb motor impairment.Main MeasuresBimanual performance was assessed using the Adult Assisting Hand Assessment Stroke. Potential predictors were collected at admission through comprehensive clinical and functional assessments. We used multivariate linear regression to identify key predictors and a Chi-square Automatic Interaction Detection analysis to derive a clinical decision tree.ResultsNinety-two participants (mean age 67 ± 12 years; 22 ± 8 days post-stroke) participated. Bimanual performance improved over time (p < 0.001), with median scores increasing from 8 (interquartile range 0-52) at admission to 48 (8-70) at 6 months, and 48 (8-75) at 12 months. At 6 months, admission grasp function and stroke severity (64% and 9%) jointly explained 73% of the variance in bimanual performance scores. At 12 months, admission stroke severity, grasp function, and Barthel Index (66%, 10%, and 2%) accounted for 78% of the variance. Decision tree analysis confirmed stroke severity and grasp function as the primary predictors and generated a clinically interpretable model.ConclusionBimanual performance improves most within the first 6 months post-stroke. Grasp function and stroke severity at admission strongly predict long-term bimanual outcomes. The decision tree derived from the Chi-square Automatic Interaction Detection analysis may support stratified rehabilitation and realistic goal-setting for daily bimanual use.
{"title":"Tracking bimanual recovery after stroke: Grasp function and stroke severity predict 1-year performance.","authors":"Annick Van Gils, Yue Zou, Sarah Meyer, Marc Michielsen, Christophe Lafosse, Hilde Beyens, Fabienne Schillebeeckx, Daphne Kos, Geert Verheyden","doi":"10.1177/02692155251391669","DOIUrl":"https://doi.org/10.1177/02692155251391669","url":null,"abstract":"<p><p>ObjectiveTo characterize the trajectory and identify early predictors of bimanual performance at 6 and 12 months post-stroke.DesignProspective longitudinal study with assessments at admission, 6, and 12 months post-stroke.SettingInpatient rehabilitation centre.ParticipantsFirst-ever stroke survivors with unilateral upper limb motor impairment.Main MeasuresBimanual performance was assessed using the Adult Assisting Hand Assessment Stroke. Potential predictors were collected at admission through comprehensive clinical and functional assessments. We used multivariate linear regression to identify key predictors and a Chi-square Automatic Interaction Detection analysis to derive a clinical decision tree.ResultsNinety-two participants (mean age 67 ± 12 years; 22 ± 8 days post-stroke) participated. Bimanual performance improved over time (<i>p</i> < 0.001), with median scores increasing from 8 (interquartile range 0-52) at admission to 48 (8-70) at 6 months, and 48 (8-75) at 12 months. At 6 months, admission grasp function and stroke severity (64% and 9%) jointly explained 73% of the variance in bimanual performance scores. At 12 months, admission stroke severity, grasp function, and Barthel Index (66%, 10%, and 2%) accounted for 78% of the variance. Decision tree analysis confirmed stroke severity and grasp function as the primary predictors and generated a clinically interpretable model.ConclusionBimanual performance improves most within the first 6 months post-stroke. Grasp function and stroke severity at admission strongly predict long-term bimanual outcomes. The decision tree derived from the Chi-square Automatic Interaction Detection analysis may support stratified rehabilitation and realistic goal-setting for daily bimanual use.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"2692155251391669"},"PeriodicalIF":2.9,"publicationDate":"2025-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145421313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}