Pub Date : 2026-01-14DOI: 10.1097/MRR.0000000000000695
Dobrivoje S Stokic
{"title":"In memoriam: Milan R. Dimitrijević - visionary and pioneer of neuroscience in rehabilitation.","authors":"Dobrivoje S Stokic","doi":"10.1097/MRR.0000000000000695","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000695","url":null,"abstract":"","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145965861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-08DOI: 10.1097/MRR.0000000000000691
Marleen Flim, Ingrid D van Iperen, Robert van der Stoep, Peter E Spronk
Few digital health interventions are currently used in the rehabilitation of ICU patients, despite growing interest in innovative approaches such as exergaming. We aimed to determine the requirements for a therapeutic exergaming system for use in ICU patients. A cross-sectional survey was developed through iterative feedback from a multidisciplinary panel of ICU professionals. The survey was distributed online among ICU professionals using convenience and snowball sampling. The survey was completed by 106 ICU professionals from 16 different countries across four continents. The willingness to use a therapeutic exergaming system to increase physical activity in ICU patients was high, with a median score of 9 (interquartile range: 7-10) on a 0-10 scale. System features rated as very important or absolutely essential included ease of use (85%), patient enjoyment (85%), increasing the patients' motivation for physical activity and mobility (84%), and the ease of transportation (82%). Respondents emphasized adaptability to physical, cognitive, and sensory impairments, suitability for bedridden patients, and ease of integration within the ICU environment, including hygiene, mobility, and space constraints. Over 80% of respondents (strongly) agreed with most proposed benefits of therapeutic exergaming, including stimulation of active participation (94%), activation of patients with ICU-acquired weakness or prolonged immobilization (91%), distraction from the ICU environment (91%), and improved patient motivation to engage in rehabilitation (82%). This survey identifies key requirements for the development of therapeutic exergaming systems and supports their potential role in ICU mobilization when designed to complement existing rehabilitation practices and the intensive care context.
{"title":"Challenges in developing a new therapeutic exergaming system to promote mobility in ICU patients: an international survey exploring needs and success factors.","authors":"Marleen Flim, Ingrid D van Iperen, Robert van der Stoep, Peter E Spronk","doi":"10.1097/MRR.0000000000000691","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000691","url":null,"abstract":"<p><p>Few digital health interventions are currently used in the rehabilitation of ICU patients, despite growing interest in innovative approaches such as exergaming. We aimed to determine the requirements for a therapeutic exergaming system for use in ICU patients. A cross-sectional survey was developed through iterative feedback from a multidisciplinary panel of ICU professionals. The survey was distributed online among ICU professionals using convenience and snowball sampling. The survey was completed by 106 ICU professionals from 16 different countries across four continents. The willingness to use a therapeutic exergaming system to increase physical activity in ICU patients was high, with a median score of 9 (interquartile range: 7-10) on a 0-10 scale. System features rated as very important or absolutely essential included ease of use (85%), patient enjoyment (85%), increasing the patients' motivation for physical activity and mobility (84%), and the ease of transportation (82%). Respondents emphasized adaptability to physical, cognitive, and sensory impairments, suitability for bedridden patients, and ease of integration within the ICU environment, including hygiene, mobility, and space constraints. Over 80% of respondents (strongly) agreed with most proposed benefits of therapeutic exergaming, including stimulation of active participation (94%), activation of patients with ICU-acquired weakness or prolonged immobilization (91%), distraction from the ICU environment (91%), and improved patient motivation to engage in rehabilitation (82%). This survey identifies key requirements for the development of therapeutic exergaming systems and supports their potential role in ICU mobilization when designed to complement existing rehabilitation practices and the intensive care context.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145932814","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Neurolathyrism causes lifelong, incurable spastic paralysis of the lower limbs and permanent disability. Evidence on its impact on daily functioning and quality of life is limited. This study assessed functional impairment among people with neurolathyrism in grass pea-growing districts of Amhara, Ethiopia. A community-based cross-sectional quantitative study was conducted among 346 individuals diagnosed with neurolathyrism from grass pea-producing districts of the Amhara National Regional State. Functional impairment was assessed using the 12-item, interviewer-administered WHO Disability Assessment Schedule. Thirty-five trained BSc nurses collected data using tablets with Kobo Collect v2024.1.3. Data were analyzed using STATA 17, applying descriptive statistics and ordinary logistic regression. More than half of the participants reported severe functional impairment. Mobility was most affected (79.2%), with nearly nine in 10 experiencing difficulties. Participants aged 45-54 years had over twice the odds of functional disability compared with those aged 18-25 years [adjusted odds ratio (AOR) = 2.3, 95% confidence interval (CI): 1.0-5.3]. Men were more likely to experience functional disability than women (AOR = 1.9, 95% CI: 1.2-2.9). Living with neurolathyrism for 21-25 years was also significantly associated with higher odds of functional disability. Being married was protective compared with being unmarried (AOR = 0.5, 95% CI: 0.3-0.9), and those who sought spiritual treatment were 63% less likely to report functional disability (AOR = 0.4, 95% CI: 0.2-0.6). These findings show that neurolathyrism places a significant long-term burden on adults, particularly affecting mobility and self-care, highlighting the need for targeted rehabilitation and sustained support.
{"title":"Functional impairment among adults with neurolathyrism-related spastic paraparesis in Amhara National Regional State, Ethiopia.","authors":"Azeb Atnafu Getie, Solomon Mekonnen Abebe, Tadesse Awoke Ayelee, Telake Azale, Netsanet Worku","doi":"10.1097/MRR.0000000000000694","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000694","url":null,"abstract":"<p><p>Neurolathyrism causes lifelong, incurable spastic paralysis of the lower limbs and permanent disability. Evidence on its impact on daily functioning and quality of life is limited. This study assessed functional impairment among people with neurolathyrism in grass pea-growing districts of Amhara, Ethiopia. A community-based cross-sectional quantitative study was conducted among 346 individuals diagnosed with neurolathyrism from grass pea-producing districts of the Amhara National Regional State. Functional impairment was assessed using the 12-item, interviewer-administered WHO Disability Assessment Schedule. Thirty-five trained BSc nurses collected data using tablets with Kobo Collect v2024.1.3. Data were analyzed using STATA 17, applying descriptive statistics and ordinary logistic regression. More than half of the participants reported severe functional impairment. Mobility was most affected (79.2%), with nearly nine in 10 experiencing difficulties. Participants aged 45-54 years had over twice the odds of functional disability compared with those aged 18-25 years [adjusted odds ratio (AOR) = 2.3, 95% confidence interval (CI): 1.0-5.3]. Men were more likely to experience functional disability than women (AOR = 1.9, 95% CI: 1.2-2.9). Living with neurolathyrism for 21-25 years was also significantly associated with higher odds of functional disability. Being married was protective compared with being unmarried (AOR = 0.5, 95% CI: 0.3-0.9), and those who sought spiritual treatment were 63% less likely to report functional disability (AOR = 0.4, 95% CI: 0.2-0.6). These findings show that neurolathyrism places a significant long-term burden on adults, particularly affecting mobility and self-care, highlighting the need for targeted rehabilitation and sustained support.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-08DOI: 10.1097/MRR.0000000000000690
Susan Winifred Hunter, Kristin Nugent, Ricardo Viana, Sander L Hitzig, Crystal MacKay, Amanda Mayo, Steven Dilkas, William C Miller, Michael W Payne
The purpose of this cross-sectional, web-based survey was to identify environmental barriers to accessibility experienced by people with lower limb loss and evaluate the association between environmental barriers and quality of life. Eligibility criteria include people aged 18 years old, have a major lower limb loss (at the ankle or above), greater than or equal to 3 months post-amputation surgery, using a prosthesis for mobility (beyond transfers), are no longer receiving prosthesis-related rehabilitation care, and understand English. Demographic and clinical characteristics were collected through self-report. Outcome measures collected were the Prosthesis Evaluation Questionnaire Mobility Scale, Perceived Environmental Barriers to Outdoor Mobility Scale, Craig Hospital Inventory of Environmental Factors, and WHO Quality of Life-Brief Questionnaire. Descriptive statistics summarized clinical, demographic, and survey variables. Simple linear regression modeling evaluated the association between environmental barriers and quality of life. Seventy-eight [mean age: 59.3 (14.0) years, 67% male, and 59% transtibial] individuals participated. A one-unit increase on the Craig Hospital Inventory of Environmental Factors Scale, indicating greater environmental barriers to mobility, was significantly associated with an 8.07 decrease on the WHO Quality of Life-Brief (95% confidence interval: -15.46 to -0.68, R2 = 0.38). A safe and barrier-free environment is crucial for accessibility following lower limb loss. Future research should enhance accessibility through collaboration among end users, clinicians, and policymakers to address the built environmental needs of this population.
{"title":"Environmental barriers and impact on quality of life in adults with lower limb loss in Canada.","authors":"Susan Winifred Hunter, Kristin Nugent, Ricardo Viana, Sander L Hitzig, Crystal MacKay, Amanda Mayo, Steven Dilkas, William C Miller, Michael W Payne","doi":"10.1097/MRR.0000000000000690","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000690","url":null,"abstract":"<p><p>The purpose of this cross-sectional, web-based survey was to identify environmental barriers to accessibility experienced by people with lower limb loss and evaluate the association between environmental barriers and quality of life. Eligibility criteria include people aged 18 years old, have a major lower limb loss (at the ankle or above), greater than or equal to 3 months post-amputation surgery, using a prosthesis for mobility (beyond transfers), are no longer receiving prosthesis-related rehabilitation care, and understand English. Demographic and clinical characteristics were collected through self-report. Outcome measures collected were the Prosthesis Evaluation Questionnaire Mobility Scale, Perceived Environmental Barriers to Outdoor Mobility Scale, Craig Hospital Inventory of Environmental Factors, and WHO Quality of Life-Brief Questionnaire. Descriptive statistics summarized clinical, demographic, and survey variables. Simple linear regression modeling evaluated the association between environmental barriers and quality of life. Seventy-eight [mean age: 59.3 (14.0) years, 67% male, and 59% transtibial] individuals participated. A one-unit increase on the Craig Hospital Inventory of Environmental Factors Scale, indicating greater environmental barriers to mobility, was significantly associated with an 8.07 decrease on the WHO Quality of Life-Brief (95% confidence interval: -15.46 to -0.68, R2 = 0.38). A safe and barrier-free environment is crucial for accessibility following lower limb loss. Future research should enhance accessibility through collaboration among end users, clinicians, and policymakers to address the built environmental needs of this population.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145932773","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-08DOI: 10.1097/MRR.0000000000000692
Sofie Leunis, Hanne Van Criekinge, Leen Schepers, Margaux Segal, Kristel De Paepe, Jessia Dever, Frederik Hoffmann, Henri Monbailliu, Leen Pollet, Wim Laleman, Schalk Van der Merwe, Hannah Van Malenstein, Jef Verbeek, Chris Verslype, Mauricio Sainz Barriga, Jacques Pirenne, Diethard Monbaliu
Sarcopenia and frailty are common in liver transplant candidates and often deteriorate early posttransplantation, negatively affecting recovery and survival. Since 5 years, we refer liver transplant recipients who, despite being medically stable, are considered unfit for safe discharge home because of physical, social, or functional limitations for continued care at an independent rehabilitation hospital. This retrospective observational study evaluated safety and functional outcomes of this rehabilitation program and explored clinical characteristics associated with referral. We reviewed all adult liver transplant recipients at University Hospitals Leuven between July 2020 and 2025. Collected data included demographics, frailty, BMI, neuropathy, laboratory model for end-stage liver disease/Stanford Integrated Psychosocial Assessment for Transplant scores, ICU/hospital length of stay, and referral for inpatient rehabilitation. For referred patients, rehabilitation duration and functional outcomes were analyzed. Of 380 liver transplant recipients, 34 (8.9%) were referred for inpatient rehabilitation. Median rehabilitation duration was 30 days [interquartile range (IQR): 21-40]. Significant functional improvements were observed, with 6-min walk distance increasing from 130 (IQR: 33-225) to 300 (IQR: 220-423; P ≤ 0.001) m, and Tinetti scores improving from 21 (IQR: 18-23) to 25 (IQR: 22-27; P = 0.001). No mortality occurred during rehabilitation. Four patients were readmitted for reasons unrelated to rehabilitation. Multivariable logistic regression identified lower pretransplant BMI and higher frailty scores as independent predictors of referral, with a trend toward an association with peroneal neuropathy. Continued inpatient rehabilitation following liver transplant is feasible, safe, and associated with clinically relevant functional improvements. Pretransplant malnutrition and frailty, as well as posttransplant peroneal neuropathy, may represent targets to facilitate posttransplant recovery.
{"title":"Inpatient functional rehabilitation after liver transplantation: clinical benefit for functional recovery and indicators for early intervention - a retrospective observational study.","authors":"Sofie Leunis, Hanne Van Criekinge, Leen Schepers, Margaux Segal, Kristel De Paepe, Jessia Dever, Frederik Hoffmann, Henri Monbailliu, Leen Pollet, Wim Laleman, Schalk Van der Merwe, Hannah Van Malenstein, Jef Verbeek, Chris Verslype, Mauricio Sainz Barriga, Jacques Pirenne, Diethard Monbaliu","doi":"10.1097/MRR.0000000000000692","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000692","url":null,"abstract":"<p><p>Sarcopenia and frailty are common in liver transplant candidates and often deteriorate early posttransplantation, negatively affecting recovery and survival. Since 5 years, we refer liver transplant recipients who, despite being medically stable, are considered unfit for safe discharge home because of physical, social, or functional limitations for continued care at an independent rehabilitation hospital. This retrospective observational study evaluated safety and functional outcomes of this rehabilitation program and explored clinical characteristics associated with referral. We reviewed all adult liver transplant recipients at University Hospitals Leuven between July 2020 and 2025. Collected data included demographics, frailty, BMI, neuropathy, laboratory model for end-stage liver disease/Stanford Integrated Psychosocial Assessment for Transplant scores, ICU/hospital length of stay, and referral for inpatient rehabilitation. For referred patients, rehabilitation duration and functional outcomes were analyzed. Of 380 liver transplant recipients, 34 (8.9%) were referred for inpatient rehabilitation. Median rehabilitation duration was 30 days [interquartile range (IQR): 21-40]. Significant functional improvements were observed, with 6-min walk distance increasing from 130 (IQR: 33-225) to 300 (IQR: 220-423; P ≤ 0.001) m, and Tinetti scores improving from 21 (IQR: 18-23) to 25 (IQR: 22-27; P = 0.001). No mortality occurred during rehabilitation. Four patients were readmitted for reasons unrelated to rehabilitation. Multivariable logistic regression identified lower pretransplant BMI and higher frailty scores as independent predictors of referral, with a trend toward an association with peroneal neuropathy. Continued inpatient rehabilitation following liver transplant is feasible, safe, and associated with clinically relevant functional improvements. Pretransplant malnutrition and frailty, as well as posttransplant peroneal neuropathy, may represent targets to facilitate posttransplant recovery.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-08DOI: 10.1097/MRR.0000000000000688
Annika Miikkulainen, Mikhail Saltychev, Sara Widbom-Kolhanen, Juhani Juhola, Hanna-Stiina Taskinen
The objective of this retrospective cross-sectional register-based study among 1597 patients with electromyography-confirmed carpal tunnel syndrome (CTS) was to evaluate the psychometric properties of the quick disabilities of the arm, shoulder, and hand questionnaire (QuickDASH). Two-parameter item response theory analysis with a rating scale model was applied. Of the respondents, 896 (56%) were women. The average age was 55.0 (SD: 16.3) years. Mean QuickDASH score was 38.0 (SD: 23.2%) points. For difficulty parameter estimates, some items demonstrated a slight shift to the right toward higher QuickDASH scores. The intervals between the difficulty estimates across all scoring options were highly similar, exhibiting only minor fluctuation. Overall, the test characteristic curve for the entire QuickDASH showed a slight shift toward worse disability and higher scores. Item discrimination estimates ranged from moderate 1.20 to perfect 3.31. For 9 out of 11 items, the discrimination estimates were perfect, that is, greater than 1.7. Overall, QuickDASH demonstrated consistent difficulty across item response options and good ability to differentiate between respondents with varying degrees of functional limitations. In other words, QuickDASH in this sample proved to be a measure that was well able to distinguish patients at different levels of functional limitations caused by CTS. A modest shift toward higher disability levels was observed for most of the items and for the overall scale, suggesting that patients might tend to underestimate their disability severity assessed by QuickDASH. However, this shift was so mild that it would hardly be of any significance in a typical clinical situation.
{"title":"Psychometric properties of quick disabilities of the arm, shoulder, and hand questionnaire among people with carpal tunnel syndrome: item response theory analysis.","authors":"Annika Miikkulainen, Mikhail Saltychev, Sara Widbom-Kolhanen, Juhani Juhola, Hanna-Stiina Taskinen","doi":"10.1097/MRR.0000000000000688","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000688","url":null,"abstract":"<p><p>The objective of this retrospective cross-sectional register-based study among 1597 patients with electromyography-confirmed carpal tunnel syndrome (CTS) was to evaluate the psychometric properties of the quick disabilities of the arm, shoulder, and hand questionnaire (QuickDASH). Two-parameter item response theory analysis with a rating scale model was applied. Of the respondents, 896 (56%) were women. The average age was 55.0 (SD: 16.3) years. Mean QuickDASH score was 38.0 (SD: 23.2%) points. For difficulty parameter estimates, some items demonstrated a slight shift to the right toward higher QuickDASH scores. The intervals between the difficulty estimates across all scoring options were highly similar, exhibiting only minor fluctuation. Overall, the test characteristic curve for the entire QuickDASH showed a slight shift toward worse disability and higher scores. Item discrimination estimates ranged from moderate 1.20 to perfect 3.31. For 9 out of 11 items, the discrimination estimates were perfect, that is, greater than 1.7. Overall, QuickDASH demonstrated consistent difficulty across item response options and good ability to differentiate between respondents with varying degrees of functional limitations. In other words, QuickDASH in this sample proved to be a measure that was well able to distinguish patients at different levels of functional limitations caused by CTS. A modest shift toward higher disability levels was observed for most of the items and for the overall scale, suggesting that patients might tend to underestimate their disability severity assessed by QuickDASH. However, this shift was so mild that it would hardly be of any significance in a typical clinical situation.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145933093","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-08DOI: 10.1097/MRR.0000000000000689
Silvija Mahnik, Ana Aljinović, Alan Mahnik, Pero Hrabač, Monika Žabčić, Ivan Bojanić
Quadriceps muscle weakness is a common clinical feature in individuals with knee osteoarthritis (KOA) and contributes to pain, functional limitations, and reduced quality of life. While quadriceps strengthening exercises are well-established, the additional benefits of electromyographic biofeedback (EMG-BFB) and neuromuscular electrical stimulation (NMES) remain inconclusive. This single-blind randomized controlled trial investigated whether EMG-BFB or NMES provides added benefits when combined with isometric quadriceps strengthening exercises in patients with mild-to-moderate KOA. Ninety-three participants aged over 55 years, meeting the American College of Rheumatology criteria and classified as Kellgren-Lawrence grades 1-2, were randomly assigned to three groups: exercise only, exercise plus EMG-BFB, and exercise plus NMES. All participants completed 15 supervised sessions over 3 weeks. Pain intensity (Visual Analogue Scale) was the primary outcome. Secondary outcomes included physical function (Western Ontario and McMaster Universities Osteoarthritis Index), muscle activation (raw EMG amplitude), and quality of life (36-Item Short Form Health Survey), assessed at baseline, immediately after the intervention, and at 3- and 6-month follow-up. All groups demonstrated significant improvements in pain, knee function, muscle activation, and quality of life following the intervention, with benefits maintained at follow-up. However, no significant differences were observed between groups at any time point. These results suggest that isometric quadriceps strengthening exercises alone are effective in managing KOA, while the addition of EMG-BFB or NMES does not yield superior clinical outcomes. Given the simplicity, accessibility, and effectiveness of exercise alone, it may serve as a first-line intervention, while the specific clinical indications for adding EMG-BFB and NMES to isometric exercises remain to be determined.
{"title":"Electromyographic biofeedback or neuromuscular electrical stimulation added to isometric quadriceps exercise does not improve pain and functional outcomes in knee osteoarthritis: a randomized controlled trial.","authors":"Silvija Mahnik, Ana Aljinović, Alan Mahnik, Pero Hrabač, Monika Žabčić, Ivan Bojanić","doi":"10.1097/MRR.0000000000000689","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000689","url":null,"abstract":"<p><p>Quadriceps muscle weakness is a common clinical feature in individuals with knee osteoarthritis (KOA) and contributes to pain, functional limitations, and reduced quality of life. While quadriceps strengthening exercises are well-established, the additional benefits of electromyographic biofeedback (EMG-BFB) and neuromuscular electrical stimulation (NMES) remain inconclusive. This single-blind randomized controlled trial investigated whether EMG-BFB or NMES provides added benefits when combined with isometric quadriceps strengthening exercises in patients with mild-to-moderate KOA. Ninety-three participants aged over 55 years, meeting the American College of Rheumatology criteria and classified as Kellgren-Lawrence grades 1-2, were randomly assigned to three groups: exercise only, exercise plus EMG-BFB, and exercise plus NMES. All participants completed 15 supervised sessions over 3 weeks. Pain intensity (Visual Analogue Scale) was the primary outcome. Secondary outcomes included physical function (Western Ontario and McMaster Universities Osteoarthritis Index), muscle activation (raw EMG amplitude), and quality of life (36-Item Short Form Health Survey), assessed at baseline, immediately after the intervention, and at 3- and 6-month follow-up. All groups demonstrated significant improvements in pain, knee function, muscle activation, and quality of life following the intervention, with benefits maintained at follow-up. However, no significant differences were observed between groups at any time point. These results suggest that isometric quadriceps strengthening exercises alone are effective in managing KOA, while the addition of EMG-BFB or NMES does not yield superior clinical outcomes. Given the simplicity, accessibility, and effectiveness of exercise alone, it may serve as a first-line intervention, while the specific clinical indications for adding EMG-BFB and NMES to isometric exercises remain to be determined.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145932845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-04DOI: 10.1097/MRR.0000000000000687
Aryane C Silva, Kênia K P Menezes, Carolina L A Soares, Ludmilla R Batista, Iza Faria-Fortini, Christina D C M Faria
The objective was to determine whether depressive symptoms, self-reported manual ability, self-reported locomotion ability, and functional independence, assessed at 6 months after stroke, are predictors of generic and specific health-related quality of life (HRQoL) at 24 months after stroke. This is a prospective longitudinal study with individuals with and without previous disability. The dependent variables, assessed at 24 months after stroke, were generic [short form-36 (SF-36)] and specific (stroke-specific quality of life) HRQoL. Potential predictors, assessed at 6 months after stroke, were: depressive symptoms (Geriatric Depression Scale), self-reported manual (ABILHAND) and locomotor (ABILOCO) abilities, and functional independence (Modified Barthel Index). Multiple linear regression analyses were employed to identify the potential predictors of generic (model-1) and specific (model-2) HRQoL (α = 5%). Sixty-eight individuals were evaluated at both 6 and 24 months after stroke (59 years, SD 13). The regression analysis showed that the self-reported manual ability and depressive symptoms at 6 months after stroke were significant predictors of generic (R2 = 26.1%; F = 24.96; P = 0.001) and specific (R2 = 26.4%; F = 25.332; P = 0.002) HRQoL at 24 months poststroke. Self-reported manual ability and depressive symptoms, at 6 months after stroke, are predictors of HRQoL at 24 months. Thus, these outcomes are important to be considered in the immediate chronic phase of the stroke since individuals with worse self-reported manual ability and presence of depressive symptoms are at risk of experiencing worse HRQoL in the late chronic phase.
目的是确定中风后6个月评估的抑郁症状、自我报告的体力能力、自我报告的运动能力和功能独立性是否为中风后24个月的一般和特定健康相关生活质量(HRQoL)的预测因子。这是一项前瞻性纵向研究,研究对象包括有或无既往残疾的个体。卒中后24个月评估的因变量为通用[SF-36]和特定(卒中特异性生活质量)HRQoL。中风后6个月评估的潜在预测因素包括:抑郁症状(老年抑郁量表)、自我报告的体力(ABILHAND)和运动能力(ABILOCO)以及功能独立性(修正Barthel指数)。采用多元线性回归分析确定通用(模型-1)和特定(模型-2)HRQoL (α = 5%)的潜在预测因子。68名患者在中风后6个月和24个月(59年,标准差13)接受评估。回归分析显示,卒中后6个月自我报告的体力活动能力和抑郁症状是卒中后24个月通用HRQoL (R2 = 26.1%; F = 24.96; P = 0.001)和特定HRQoL (R2 = 26.4%; F = 25.332; P = 0.002)的显著预测因子。中风后6个月自述的体力和抑郁症状是24个月HRQoL的预测因子。因此,在中风的直接慢性期考虑这些结果是很重要的,因为自述体力能力较差和存在抑郁症状的个体在慢性期晚期有经历较差HRQoL的风险。
{"title":"Self-reported manual ability and depressive symptoms, at six months after stroke, predict health-related quality of life at 24 months after stroke.","authors":"Aryane C Silva, Kênia K P Menezes, Carolina L A Soares, Ludmilla R Batista, Iza Faria-Fortini, Christina D C M Faria","doi":"10.1097/MRR.0000000000000687","DOIUrl":"https://doi.org/10.1097/MRR.0000000000000687","url":null,"abstract":"<p><p>The objective was to determine whether depressive symptoms, self-reported manual ability, self-reported locomotion ability, and functional independence, assessed at 6 months after stroke, are predictors of generic and specific health-related quality of life (HRQoL) at 24 months after stroke. This is a prospective longitudinal study with individuals with and without previous disability. The dependent variables, assessed at 24 months after stroke, were generic [short form-36 (SF-36)] and specific (stroke-specific quality of life) HRQoL. Potential predictors, assessed at 6 months after stroke, were: depressive symptoms (Geriatric Depression Scale), self-reported manual (ABILHAND) and locomotor (ABILOCO) abilities, and functional independence (Modified Barthel Index). Multiple linear regression analyses were employed to identify the potential predictors of generic (model-1) and specific (model-2) HRQoL (α = 5%). Sixty-eight individuals were evaluated at both 6 and 24 months after stroke (59 years, SD 13). The regression analysis showed that the self-reported manual ability and depressive symptoms at 6 months after stroke were significant predictors of generic (R2 = 26.1%; F = 24.96; P = 0.001) and specific (R2 = 26.4%; F = 25.332; P = 0.002) HRQoL at 24 months poststroke. Self-reported manual ability and depressive symptoms, at 6 months after stroke, are predictors of HRQoL at 24 months. Thus, these outcomes are important to be considered in the immediate chronic phase of the stroke since individuals with worse self-reported manual ability and presence of depressive symptoms are at risk of experiencing worse HRQoL in the late chronic phase.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":""},"PeriodicalIF":1.3,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145668029","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Technological and social advances have improved prosthetic devices; however, discomfort during prosthesis use remains a persistent problem. Therefore, ongoing assessment of socket fit is essential. This process is key to ensuring long-term functionality and comfort for prosthetic users. This study aimed to adapt the Comprehensive Lower-limb Amputee Socket Survey (CLASS) into Turkish and evaluate its validity and reliability in individuals with combat-related unilateral lower-limb amputation at K3 and K4 mobility levels. We performed cross-cultural adaptation and validation using multiple outcome measures reflecting various aspects of socket fit. A cross-sectional test-retest design was used with 80 prosthesis-using participants recruited from a rehabilitation hospital. Reliability was assessed using the intraclass correlation coefficient (ICC) and internal consistency via Cronbach's α . The Turkish CLASS demonstrated strong test-retest reliability across its domains (ICC = 0.80-0.90) and high internal consistency (Cronbach's α ranging from 0.73 to 0.87 across subscales). No significant floor effects were observed. Validity was examined through correlations with the Trinity Amputation and Prosthesis Experiences Scale (TAPES), Satisfaction with Prosthesis Questionnaire (SAT-PRO), and Socket Comfort Score (SCS). The comfort domain of Turkish CLASS showed strong correlations with SAT-PRO ( r = 0.62) and SCS ( r = 0.74), while other domains had moderate correlations with TAPES subscales ( r = 0.43-0.55), supporting concurrent validity. The minimum detectable change scores across the domains ranged from 9.3 (comfort) to 16.1 (appearance). These findings indicate that the Turkish CLASS is a valid and reliable instrument for assessing socket fit in unilateral lower-limb amputees and is suitable for routine clinical use.
{"title":"A multidimensional validation study of the Turkish version of the Comprehensive Lower-limb Amputee Socket Survey in veterans.","authors":"Ceren Kuzu, Yasin Demir, Sevilay Karahan, Semra Topuz","doi":"10.1097/MRR.0000000000000683","DOIUrl":"10.1097/MRR.0000000000000683","url":null,"abstract":"<p><p>Technological and social advances have improved prosthetic devices; however, discomfort during prosthesis use remains a persistent problem. Therefore, ongoing assessment of socket fit is essential. This process is key to ensuring long-term functionality and comfort for prosthetic users. This study aimed to adapt the Comprehensive Lower-limb Amputee Socket Survey (CLASS) into Turkish and evaluate its validity and reliability in individuals with combat-related unilateral lower-limb amputation at K3 and K4 mobility levels. We performed cross-cultural adaptation and validation using multiple outcome measures reflecting various aspects of socket fit. A cross-sectional test-retest design was used with 80 prosthesis-using participants recruited from a rehabilitation hospital. Reliability was assessed using the intraclass correlation coefficient (ICC) and internal consistency via Cronbach's α . The Turkish CLASS demonstrated strong test-retest reliability across its domains (ICC = 0.80-0.90) and high internal consistency (Cronbach's α ranging from 0.73 to 0.87 across subscales). No significant floor effects were observed. Validity was examined through correlations with the Trinity Amputation and Prosthesis Experiences Scale (TAPES), Satisfaction with Prosthesis Questionnaire (SAT-PRO), and Socket Comfort Score (SCS). The comfort domain of Turkish CLASS showed strong correlations with SAT-PRO ( r = 0.62) and SCS ( r = 0.74), while other domains had moderate correlations with TAPES subscales ( r = 0.43-0.55), supporting concurrent validity. The minimum detectable change scores across the domains ranged from 9.3 (comfort) to 16.1 (appearance). These findings indicate that the Turkish CLASS is a valid and reliable instrument for assessing socket fit in unilateral lower-limb amputees and is suitable for routine clinical use.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":"232-239"},"PeriodicalIF":1.3,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145244510","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-01Epub Date: 2025-10-13DOI: 10.1097/MRR.0000000000000684
Paratakorn Chalermchuang, Chanwit Phongamwong
This study aimed to determine the prevalence and associated risk factors of sarcopenia among patients with cardiovascular diseases (CVD) undergoing cardiac rehabilitation (CR) and to evaluate the diagnostic accuracy of phase angle (PhA) in identifying sarcopenia. This cross-sectional study included 100 patients with ischemic heart disease undergoing outpatient CR. Sarcopenia was diagnosed based on the criteria of the Asian Working Group for Sarcopenia 2019, which utilized measurements of muscle mass, handgrip strength, and gait speed. PhA was measured using bioelectrical impedance analysis. Multivariable logistic regression was used to identify factors associated with sarcopenia, and receiver operating characteristic (ROC) curve analysis was conducted to evaluate the diagnostic performance of PhA. The prevalence of sarcopenia in the study population was 35%, with 23% classified as having severe sarcopenia. Female sex [adjusted odds ratio (aOR) 5.9, P = 0.004] and lower BMI (aOR 0.71, P = 0.005) were significantly associated with sarcopenia. Mean PhA values were significantly lower in patients with sarcopenia compared to those without (3.61 vs. 4.47 °, P < 0.001). ROC curve analysis demonstrated good diagnostic accuracy of PhA for identifying sarcopenia, with an area under the curve of 0.83 (95% confidence intervals: 0.75-0.91). The optimal PhA cutoff value to distinguish sarcopenia was 4.01 °, yielding both sensitivity and specificity of 80%. Sarcopenia was prevalent among CVD patients undergoing CR, with female gender and lower BMI as significant risk factors. PhA demonstrated high diagnostic accuracy for detecting sarcopenia and may serve as a useful, noninvasive tool in clinical settings.
本研究旨在确定接受心脏康复(CR)的心血管疾病(CVD)患者肌少症的患病率及相关危险因素,并评估相位角(PhA)诊断肌少症的准确性。这项横断面研究包括100名接受门诊CR的缺血性心脏病患者,根据2019年亚洲肌肉减少症工作组的标准诊断肌肉减少症,该标准利用肌肉质量、握力和步态速度的测量。PhA采用生物电阻抗分析法测定。采用多变量logistic回归确定与肌少症相关的因素,并采用受试者工作特征(ROC)曲线分析评价PhA的诊断效能。研究人群中肌肉减少症的患病率为35%,其中23%被归类为严重肌肉减少症。女性[校正优势比(aOR) 5.9, P = 0.004]和较低的BMI (aOR 0.71, P = 0.005)与肌肉减少症显著相关。肌少症患者的平均PhA值明显低于无肌少症患者(3.61°vs. 4.47°,P
{"title":"Prevalence, associated factors, and bioelectrical impedance phase angle measurement for sarcopenia in patients undergoing cardiac rehabilitation.","authors":"Paratakorn Chalermchuang, Chanwit Phongamwong","doi":"10.1097/MRR.0000000000000684","DOIUrl":"10.1097/MRR.0000000000000684","url":null,"abstract":"<p><p>This study aimed to determine the prevalence and associated risk factors of sarcopenia among patients with cardiovascular diseases (CVD) undergoing cardiac rehabilitation (CR) and to evaluate the diagnostic accuracy of phase angle (PhA) in identifying sarcopenia. This cross-sectional study included 100 patients with ischemic heart disease undergoing outpatient CR. Sarcopenia was diagnosed based on the criteria of the Asian Working Group for Sarcopenia 2019, which utilized measurements of muscle mass, handgrip strength, and gait speed. PhA was measured using bioelectrical impedance analysis. Multivariable logistic regression was used to identify factors associated with sarcopenia, and receiver operating characteristic (ROC) curve analysis was conducted to evaluate the diagnostic performance of PhA. The prevalence of sarcopenia in the study population was 35%, with 23% classified as having severe sarcopenia. Female sex [adjusted odds ratio (aOR) 5.9, P = 0.004] and lower BMI (aOR 0.71, P = 0.005) were significantly associated with sarcopenia. Mean PhA values were significantly lower in patients with sarcopenia compared to those without (3.61 vs. 4.47 °, P < 0.001). ROC curve analysis demonstrated good diagnostic accuracy of PhA for identifying sarcopenia, with an area under the curve of 0.83 (95% confidence intervals: 0.75-0.91). The optimal PhA cutoff value to distinguish sarcopenia was 4.01 °, yielding both sensitivity and specificity of 80%. Sarcopenia was prevalent among CVD patients undergoing CR, with female gender and lower BMI as significant risk factors. PhA demonstrated high diagnostic accuracy for detecting sarcopenia and may serve as a useful, noninvasive tool in clinical settings.</p>","PeriodicalId":14301,"journal":{"name":"International Journal of Rehabilitation Research","volume":" ","pages":"205-209"},"PeriodicalIF":1.3,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145372606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}