Clinical RehabilitationPub Date : 2024-10-01Epub Date: 2024-08-06DOI: 10.1177/02692155241267205
Louise Johnson, Jane Burridge, Sean Ewings, Sara Demain
{"title":"A pilot cluster randomised controlled trial, of an IMPlicit learning approach versus standard care, on recovery of mobility following stroke (IMPS).","authors":"Louise Johnson, Jane Burridge, Sean Ewings, Sara Demain","doi":"10.1177/02692155241267205","DOIUrl":"10.1177/02692155241267205","url":null,"abstract":"<p><strong>Objectives: </strong>To evaluate the delivery of rehabilitation using implicit motor learning principles in an acute stroke setting.</p><p><strong>Design: </strong>Pilot, assessor-blind, cluster randomised controlled trial with nested qualitative evaluation.</p><p><strong>Setting: </strong>Eight inpatient stroke units, UK.</p><p><strong>Participants: </strong>People within 14 days of stroke onset, presenting with lower limb hemiplegia.</p><p><strong>Interventions: </strong>Participants at control clusters received usual care. Participants at intervention clusters received rehabilitation using an Implicit Learning Approach (ILA); primarily consisting of reduced frequency instructions/feedback, and promotion of an external focus of attention. Video recording was used to understand the ability of intervention site therapists to adhere to the implicit learning principles, and to compare differences between groups.</p><p><strong>Measures: </strong>Ability to recruit and retain clusters/participants; suitability and acceptability of data collection processes; appropriateness of fidelity monitoring methods; and appropriateness of chosen outcome measures.</p><p><strong>Results: </strong>Eight stroke units participated, with four assigned to each group (intervention/control). Fifty-one participants were enrolled (intervention group 21; control group 30). Mean time since stroke was 6 days (SD 3.42; 0-14); mean age was 73 years (SD 14, 25-94). Of those approached to take part, 72% agreed. We found clear differences between groups with respect to the frequency and type of instructional statement. The ILA was acceptable to both patients and therapists.</p><p><strong>Conclusion: </strong>It is feasible to evaluate the application and effectiveness of motor learning principles within acute stroke rehabilitation, using a cluster randomised design. A larger study is required to evaluate the benefits of each approach; we provide a range of sample size estimates required for this.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1346-1361"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141893047","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}
Clinical RehabilitationPub Date : 2024-10-01Epub Date: 2024-07-25DOI: 10.1177/02692155241261698
Neelam Nayak, Niruthikha Mahendran, Suzanne Kuys, Sandra G Brauer
{"title":"What factors at discharge predict physical activity and walking outcomes 6 months after stroke? A systematic review.","authors":"Neelam Nayak, Niruthikha Mahendran, Suzanne Kuys, Sandra G Brauer","doi":"10.1177/02692155241261698","DOIUrl":"10.1177/02692155241261698","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to identify factors at hospital discharge that predict physical activity and walking outcomes in the first 6 months after stroke.</p><p><strong>Data sources: </strong>Searches were conducted in CINAHL (EBSCO), Web of Science, PubMed and Scopus from inception to 30 April 2024. Reference lists of included articles were manually screened to identify additional studies.</p><p><strong>Review methods: </strong>Studies of adults with stroke reporting predictors at hospital discharge and outcomes of physical activity or walking across the first 6 months after hospital discharge were included. Two reviewers independently screened titles, abstracts and reviewed full texts. Quality of included studies was assessed with Quality in Prognostic Studies screening tool. A narrative synthesis was undertaken.</p><p><strong>Results: </strong>The search strategy retrieved 7834 studies, from which 6 eligible studies were identified, including a total of 1433 participants. Overall, studies had a low risk of bias. Age, balance, walking speed and walking distance at hospital discharge predicted physical activity outcomes after stroke (<i>n</i> = 2 studies). Cognition, lower limb cycling rhythm and self-efficacy for walking at hospital discharge predicted walking outcomes after stroke (<i>n</i> = 4 studies).</p><p><strong>Conclusions: </strong>A range of factors predicted physical activity and walking outcomes 6 months after stroke. Physical capabilities at discharge appear to be a predictor of these outcomes; however, this needs to be interpreted with caution. Diverse measures and time points were used across studies to characterise physical activity and walking outcomes, highlighting the need for consistency in measurement and longitudinal studies in stroke research.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1393-1403"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528935/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141757574","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}
Clinical RehabilitationPub Date : 2024-10-01Epub Date: 2024-06-11DOI: 10.1177/02692155241258903
Declan J O'Sullivan, Lindsay M Bearne, Janas M Harrington, Jefferson R Cardoso, Joseph G McVeigh
{"title":"The effectiveness of social prescribing in the management of long-term conditions in community-based adults: A systematic review and meta-analysis.","authors":"Declan J O'Sullivan, Lindsay M Bearne, Janas M Harrington, Jefferson R Cardoso, Joseph G McVeigh","doi":"10.1177/02692155241258903","DOIUrl":"10.1177/02692155241258903","url":null,"abstract":"<p><strong>Objective: </strong>The objective of this systematic review and meta-analysis was to evaluate the effectiveness of social prescribing interventions in the management of long-term conditions in adults.</p><p><strong>Data sources: </strong>Eleven electronic databases were searched for randomised and quasi-randomised controlled trials.</p><p><strong>Review methods: </strong>Outcomes of interest were quality of life, physical activity, psychological well-being and disease-specific measures. Bias was assessed with the Cochrane Risk of Bias 2 tool. A narrative synthesis and meta-analysis were performed.</p><p><strong>Results: </strong>Twelve studies (<i>n</i> = 3566) were included in this review. Social prescribing interventions were heterogeneous and the most common risks of bias were poor blinding and high attrition. Social prescribing interventions designed to target specific long-term conditions i.e., cancer and diabetes demonstrated significant improvements in quality of life (<i>n</i> = 2 studies) and disease-specific psychological outcomes respectively (<i>n</i> = 3 studies). There was some evidence for improvement in physical activity (<i>n</i> = 2 studies) but most changes were within group only (<i>n</i> = 4 studies). Social prescribing interventions did not demonstrate any significant changes in general psychological well-being.</p><p><strong>Conclusion: </strong>Social prescribing interventions demonstrated some improvements across a range of outcomes although the quality of evidence remains poor.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1306-1320"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528982/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141305623","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}
Clinical RehabilitationPub Date : 2024-10-01Epub Date: 2024-08-02DOI: 10.1177/02692155241265886
L González-Vides, J L Hernández-Verdejo, J A Gómez-Pedrero, A Ruiz-Pomeda, P Cañadas-Suárez
{"title":"Oculomotor Behaviour in Individuals with Long COVID-19.","authors":"L González-Vides, J L Hernández-Verdejo, J A Gómez-Pedrero, A Ruiz-Pomeda, P Cañadas-Suárez","doi":"10.1177/02692155241265886","DOIUrl":"10.1177/02692155241265886","url":null,"abstract":"<p><strong>Objective: </strong>To determine, the impact of long COVID-19 on oculomotor behaviour.</p><p><strong>Design: </strong>A case-control study.</p><p><strong>Setting: </strong>Spanish Association of Persistent COVID.</p><p><strong>Participant: </strong>Participants were 75 cases (64 women, 11 men, mean age 46.4 years ±8.9) and 42 controls (22 women, 20 men, mean age 53.5 years ±13.13).</p><p><strong>Intervention: </strong>An eye-tracking test based on visual search paradigm and the Adult Developmental Eye Movement Test were used to evaluate the participants.</p><p><strong>Main measures: </strong>The primary outcomes in the Adult Developmental Eye Movement Test were horizontal reading time, vertical reading time, and their ratio. And for the eye-tracking test the time to find the target, the duration, and the number of eye fixations.</p><p><strong>Results: </strong>In cases and controls, eye movement test results were horizontal(Hadj) reading time 74.2 ± 22.7 s vs 52.0 ± 6.1 s (<i>p</i> < .0001); vertical(Vadj) reading time 67.6 ± 17.8 s vs 50.4 ± 6.9 s (<i>p</i> < .0001); Hadj/Vadj ratio 0.9 ± 0.1 vs 1.0 ± 0 (<i>p</i> = .0032), respectively; and eye-tracking test results were fixation number 11.3 ± 3.07 vs 3.51 ± 2.57 (<i>p</i> < .0001); fixation duration 2.01 ± 0.79 s vs 1.5 ± 0.4 s (<i>p</i> = .0013), and time to find target 24.5 ± 8.0 vs 18 ± 9.4 (<i>p</i> = .0034), respectively.</p><p><strong>Conclusions: </strong>Data showed a lower performance in oculomotor behaviour in people with long COVID-19, compared to healthy individuals. It cannot be affirmed an ocular musculature dysfunction; the differentiated behaviour could be associated to cognitive alterations affected in these people. Both tests used could be an useful tool for the clinical assessment of these participants. Further studies are needed to explore the utility of these procedures.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1372-1381"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141878467","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}
{"title":"Development and validation of the Unmet Needs Questionnaire for young stroke survivors.","authors":"Wen-Yu Kuo, Chen-Yin Chen, Ting-Yu Chang, Jeng Wang, Chin-Man Wang, Pei-Kwei Tsay","doi":"10.1177/02692155241270968","DOIUrl":"10.1177/02692155241270968","url":null,"abstract":"<p><strong>Objective: </strong>Owing to the lack of a suitable tool for detecting the unmet needs of young stroke survivors, this study aims to develop a validated questionnaire for evaluating these unmet needs.</p><p><strong>Design: </strong>A cross-sectional, observational research design.</p><p><strong>Setting: </strong>Chang Gung Memorial Hospital Linkou and Taoyuan branches in Taiwan.</p><p><strong>Participants: </strong>A total of 211 participants (average age 53 years; within 6 months post-stroke) completed the questionnaire.</p><p><strong>Main measures: </strong>A qualitative approach was used to create an item pool. Experts verified item suitability, and content validity was evaluated using the item content validity index. Item analysis was applied to determine item quality, and factor analysis was used to explore construct validity. In addition, parallel analysis was employed to ascertain the optimal number of factors.</p><p><strong>Results: </strong>The scale development procedure resulted in a 27-item questionnaire that assesses the unmet needs of young stroke survivors after a stroke. The item content validity index was 1.0. The Unmet Needs Questionnaire has five factors: restoring prestroke abilities and life, rehabilitation-related resources, social support and self-adjustment, economic and post-stroke life adjustment, and stroke-related information. These five factors accounted for 54% of the variance. Cronbach's alpha for the total scale was 0.91, while the alpha for the subscales ranged from 0.74 to 0.88.</p><p><strong>Conclusions: </strong>The Unmet Needs Questionnaire showed acceptable reliability and validity. It can help clinical professionals and government agencies identify stroke survivors' unmet needs and develop tailored care plans. Future research should explore the trajectory of post-stroke unmet needs using this tool.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1362-1371"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141970805","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}
Clinical RehabilitationPub Date : 2024-10-01Epub Date: 2024-07-25DOI: 10.1177/02692155241264757
Min Shen, Linlin Zhang, Chunjing Li, Xiaocen Wei, Yang Li, Hongxue Wu, Xiaobin Zhang, Shuzhong Gao, Yuning Ma, Yuxia Ma
{"title":"Repetitive transcranial magnetic stimulation as a therapy for post-stroke dysphagia: An overview of systematic reviews and meta-analysis.","authors":"Min Shen, Linlin Zhang, Chunjing Li, Xiaocen Wei, Yang Li, Hongxue Wu, Xiaobin Zhang, Shuzhong Gao, Yuning Ma, Yuxia Ma","doi":"10.1177/02692155241264757","DOIUrl":"10.1177/02692155241264757","url":null,"abstract":"<p><strong>Objective: </strong>Post-stroke dysphagia is a common swallowing disorder that occurs after a stroke, leading to an increased risk of aspiration pneumonia and malnutrition. There is a pressing need for effective and safe interventions for its rehabilitation. This review aims to answer two key scientific questions: (1) What is the efficacy of repetitive transcranial magnetic stimulation in the rehabilitation of post-stroke dysphagia? (2) Is repetitive transcranial magnetic stimulation a safe intervention for post-stroke dysphagia?</p><p><strong>Data sources: </strong>A comprehensive search was conducted across four electronic databases: PubMed, Cochrane Library, Web of Science, and Embase. The search aimed to identify relevant studies concerning our topic of interest and was completed on 28 May 2024.</p><p><strong>Review methods: </strong>In accordance with the PRISMA checklist, a comprehensive search of four databases was conducted, which identified 13 relevant systematic reviews. The inclusion criteria were systematic reviews that evaluated the efficacy and safety of repetitive transcranial magnetic stimulation for post-stroke dysphagia. Exclusion criteria were reviews that did not focus on post-stroke dysphagia or did not evaluate repetitive transcranial magnetic stimulation as a therapeutic intervention. The quality, bias, reporting, and overall evidence quality of these reviews were assessed using validated tools, including the AMSTAR 2 tool for assessing the methodological quality of systematic reviews, the ROBIS tool for assessing the risk of bias, and the GRADE approach for evaluating the overall quality of evidence. This rigorous approach ensures that our review provides a comprehensive and reliable overview of the current state of knowledge on the use of repetitive transcranial magnetic stimulation for post-stroke dysphagia.</p><p><strong>Results: </strong>The sample sizes for the individual studies included in the systematic reviews/meta-analyses ranged from 66 to 555. The total number of participants across all studies included in the overall analyses was 752. The evidence was limited by the methodological flaws and heterogeneity of the systematic reviews. The quality of the evidence varied from high to low, with most outcomes having moderate quality. Future research should adopt more rigorous, standardized, and comprehensive designs to confirm the efficacy and safety of repetitive transcranial magnetic stimulation for post-stroke dysphagia. The main reason for downgrading the evidence quality was the small sample size and high heterogeneity of the primary studies.</p><p><strong>Conclusion: </strong>This overview synthesized research on repetitive transcranial magnetic stimulation for dysphagia, aiming to inform clinical and policy decisions. However, the current evidence does not conclusively establish the safety and efficacy of repetitive transcranial magnetic stimulation for post-stroke dysphagia rehabilitation. The studi","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1289-1305"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141757573","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}
Clinical RehabilitationPub Date : 2024-10-01Epub Date: 2024-08-27DOI: 10.1177/02692155241265930
Jonathan Bayuo, Frances Kam Yuet Wong, Loretta Yuet Foon Chung
{"title":"Effect of a transitional tele-rehabilitation programme on quality of life of adult burn survivors: A randomised controlled trial.","authors":"Jonathan Bayuo, Frances Kam Yuet Wong, Loretta Yuet Foon Chung","doi":"10.1177/02692155241265930","DOIUrl":"10.1177/02692155241265930","url":null,"abstract":"<p><strong>Objective: </strong>To examine the effects of the transitional tele-rehabilitation programme on quality of life of adult burn survivors.</p><p><strong>Design: </strong>A prospective, single centre, randomised controlled trial and reported according to the Consolidated Standards of Reporting Trials (CONSORT) guidelines.</p><p><strong>Participants: </strong>Adult burn survivors aged ≥18 years with burn size ≥10% total body surface area irrespective of the depth was considered eligible to participate.</p><p><strong>Intervention: </strong>The intervention was in two phases: pre-discharge and active follow-up phase (which occurred via WeChat). In both phases, comprehensive assessment and intervention guided by the Omaha System and evidenced-based protocols guided the care delivery over an 8-week period.</p><p><strong>Main measures: </strong>The outcome of interest was quality of life. Two outcome measures were used to assess the outcome of interest: Burn Specific Health Scale-Brief (BSHS-B) and the EQ-5D-5L tools. The outcome was assessed at three time points: T0 (baseline), T1 (immediate post-intervention) and T2 (4 weeks from T1).</p><p><strong>Results: </strong>In total, 60 adult burn survivors were randomly allocated to undergo the new programme. The transitional tele-rehabilitation programme elicited statistically significant improvement in simple abilities, affect, interpersonal relationship (T2) and overall quality life (T1 and T2) measured on the BSHS-B.</p><p><strong>Conclusion: </strong>Ongoing rehabilitative care is essential to support the recovery process of burn survivors considering that some quality-of-life subscales may improve faster than others. The study findings highlight the potential of employing a social media platform to improve post-burn quality of life outcomes.</p><p><strong>Trial registration: </strong>ClinicalTrials.govNCT04517721. Registered on 20 August 2020.</p>","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":" ","pages":"1333-1345"},"PeriodicalIF":2.6,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142079499","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}
Caroline Ribeiro Tottoli, Ângela Jornada Ben, Everton Nunes da Silva, Judith E Bosmans, Maurits van Tulder, Rodrigo Luiz Carregaro
{"title":"Effectiveness of Pilates compared with home-based exercises in individuals with chronic non-specific low back pain: Randomised controlled trial","authors":"Caroline Ribeiro Tottoli, Ângela Jornada Ben, Everton Nunes da Silva, Judith E Bosmans, Maurits van Tulder, Rodrigo Luiz Carregaro","doi":"10.1177/02692155241277041","DOIUrl":"https://doi.org/10.1177/02692155241277041","url":null,"abstract":"ObjectiveTo investigate the effectiveness of a Pilates exercise program compared with home-based exercises in individuals with chronic non-specific low back pain.DesignA randomised controlled trial with a six-month follow-up.SettingRehabilitation clinic.ParticipantsOne hundred and forty-five individuals (18–50 years of age) with low back pain for ≥ 12 consecutive weeks were enrolled and randomly allocated to either Pilates ( n = 72) or home-based exercise groups ( n = 73).InterventionsMethod Pilates (Mat Pilates exercises using accessories) versus home-based exercise (postural exercises, muscle stretching and strengthening, and spine stabilisation/mobilisation), twice a week, for 6 weeks.Main measuresAssessments were performed at baseline, post-intervention, and six months follow-up. Outcomes were pain intensity, disability, and health-related quality of life.ResultsAt post-intervention, the Pilates group had significantly lower pain intensity (mean difference = −1.14; 95% CI −2.05; −0.23), less disability (mean difference = −6.7; 95% CI −11.3; −2.0), and higher health-related quality of life (mean difference = 0.102; 95% CI 0.054; 0151) compared to the home-based exercise group. At follow-up, the Pilates group had a significantly higher health-related quality of life (mean difference = 0.055; 95% CI 0.003; 0.106) compared with the home-based exercise group but there were no significant differences in pain and disability. A significant overall effect of Pilates compared to home-based exercise was found for disability (mean difference = −4.4; 95% CI −7.6; −1.1), and health-related quality of life (mean difference = 0.049; 95% CI 0.022; 0.076), but not for pain.ConclusionAlthough Pilates was significantly superior to home exercise for pain and disability, the differences were not considered clinically relevant. However, Pilates did provide significant and clinically relevant differences in utility.","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":"13 1","pages":""},"PeriodicalIF":3.0,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142265743","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}
Yuhang Zheng, Xinyou Lin, Yuehong Huang, Steven Laureys, Haibo Di
{"title":"Rasch Analysis of the Chinese Version of the Nociception Coma Scale–Revised in Patients with Prolonged Disorders of Consciousness","authors":"Yuhang Zheng, Xinyou Lin, Yuehong Huang, Steven Laureys, Haibo Di","doi":"10.1177/02692155241280524","DOIUrl":"https://doi.org/10.1177/02692155241280524","url":null,"abstract":"ObjectivesThe aim of this study was to analyze the Chinese version of the Nociception Coma Scale–Revised in patients with prolonged disorders of consciousness within the framework of Rasch modeling, including investigating the invariance of total scores across different etiologies of disorders of consciousness.DesignProspective psychometric study.ParticipantsPatients with prolonged disorders of consciousness from the Rehabilitation and Neurology units in hospital.InterventionsNone.Main Outcome MeasureThe Nociception Coma Scale–Revised was undertaken by trained raters and the Coma Recovery Scale-Revised was used to assess patients’ consciousness. The psychometric properties within the Rasch model including item-person targeting, reliability and separation, item fit, unidimensionality, and differential item functioning were assessed.Results84 patients with prolonged disorders of consciousness (mean age 53 years; mean injury 5 months; 42 with Minimally Conscious State and 42 with Unresponsive Wakefulness Syndrome) of 252 observations were enrolled in the study. Through the procedure of repeated assessment and differential item function, a lower item bias Rasch set was purified. The Rasch model assumptions were examined and met, with item reliability and validity meeting the recommended threshold.ConclusionsThe Chinese version of the Nociception Coma Scale–Revised demonstrated unidimensionality, good reliability and separation, and good item fit, but dissatisfied person fit and item-person targeting. The verbal subscale showed a notable discrepancy between person responses and the difficulty of the items, suggesting limited clinical significance.","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":"16 1","pages":""},"PeriodicalIF":3.0,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142265907","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}
{"title":"Efficacy of interferential current therapy plus exercise compared to sham interferential current plus exercise for pain relief in patients with knee osteoarthritis: A randomised controlled trial","authors":"Chalida Varapirom, Vilai Kuptniratsaikul, Rungsima Yamthed, Ananya Srisomnuek","doi":"10.1177/02692155241278949","DOIUrl":"https://doi.org/10.1177/02692155241278949","url":null,"abstract":"ObjectiveTo compare the efficacy of interferential current (IFC) therapy combined with quadriceps strengthening exercise versus sham IFC plus exercise for pain relief and functional improvement in patients with knee osteoarthritis.Study DesignDouble-blind randomised controlled trial.SettingOutpatient rehabilitation clinic.SubjectsKnee osteoarthritis patients aged 50–85 years with a pain score ≥4/10.MethodsOne hundred forty-four participants were randomly allocated into the study and control groups. The study group received 20 min of IFC therapy (carrier frequency: 4000 Hz, beat frequency: 100 Hz) five times per week for three weeks, while the control group received sham IFC following the same protocol, followed by 10 min of exercise in both groups. Outcome measures included Numeric Rating Scale for Pain, Western Ontario and McMaster Universities Index (WOMAC) score, gait speed, and EuroQol-Five Dimensions-Five Levels questionnaire assessed at baseline, Week 3, and Week 6. Adverse events and patient satisfaction were evaluated at Week 3.ResultsAt Week 3, the study group demonstrated statistical improvement compared to the control group for Numeric Rating Scale for Pain, WOMAC Total, WOMAC Pain, and WOMAC Stiffness. The mean difference (95% confidence interval) between groups was 0.76 (0.21–1.30), 0.49 (0.03–0.95), 0.63 (0.13–1.13), and 0.62 (0.04–1.20), respectively. However, the mean differences between groups were below the Minimally Clinically Important Difference values for each outcome. Additionally, there were no significant differences between groups at Week 6 for any outcome measure.ConclusionIFC had no effect on pain reduction and functional improvement in patients with mild to moderate knee osteoarthritis.","PeriodicalId":10441,"journal":{"name":"Clinical Rehabilitation","volume":"41 1","pages":"2692155241278949"},"PeriodicalIF":3.0,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142176621","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}