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Reliability and Construct Validity of Three Self-report Questionnaires Assessing Dual-Task Difficulties in People With Multiple Sclerosis: An International Study 评估多发性硬化症患者双重任务困难的三种自我报告问卷的可靠性和结构有效性:一项国际研究。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.08.024
Zuhal Abasıyanık PhD , Ludovico Pedullà PhD , Turhan Kahraman PhD , Mieke D'Hooge MSc , Carme Santoyo-Medina MSc , Bernardita Soler MD, PhD , Andrea Tacchino PhD , Renee Veldkamp PhD , Edwin-Roger Meza-Murillo MD , Areen Omar MSc , Ethel Ciampi MD , Serkan Özakbaş MD , Daphne Kos PhD , Alon Kalron PhD , Peter Feys PhD

Objective

To evaluate the reliability and validity of the dual-tasking questionnaire (DTQ), dual-task screening list (DTSL), and dual-task impact on daily life activities questionnaire (DIDA-Q).

Design

Multicenter, cross-sectional study

Setting

Persons with multiple sclerosis (pwMS) were recruited from 7 multiple sclerosis centers across 6 countries (Belgium, Chile, Italy, Israel, Spain, and Turkey).

Participants

A total of 356 pwMS (mean age 47.5±11.5y, expanded disability status scale, 3.79±1.83) were enrolled.

Interventions

Not applicable

Main Outcome Measures

The reliability (internal consistency, test-retest, and measurement error) and construct validity (structural and convergent) were assessed.

Results

The DTQ, DTSL, and DIDA-Q demonstrated excellent test-retest reliability (intraclass correlation coefficients [95% CI], 0.84 [0.80-0.87] to 0.90 [0.87-0.92]) and internal consistency (Cronbach α: 0.86-0.96). As hypothesized, the 3 questionnaires showed a strong correlation with each other, moderate-to-strong correlations with other self-report questionnaires (perceived walking difficulties, fatigue, and fear of falling), and low-to-moderate correlations with cognitive information processing speed, manual dexterity, and dual-task walking performance (walking with word list generation task), showing convergent validity. The DIDA-Q exhibited systematically superior properties. These results were also verified in subsets from 6 different countries. In the structural validity analysis, all questionnaires displayed 2 main factors, allocated as “motor-driven” and “cognitive-driven” subscales.

Conclusions

The DTQ, DTSL, and DIDA-Q have good-to-excellent measurement properties, with the highest properties observed in DIDA-Q. The use of these self-reported questionnaires can be used in research and clinical practice to assess the effect of dual-task difficulties on the daily life of ambulatory pwMS.
目的评估双重任务问卷(DTQ)、双重任务筛查表(DTSL)和双重任务对日常生活活动的影响问卷(DIDA-Q)的可靠性和有效性:多中心横断面研究:从六个国家(比利时、智利、意大利、以色列、西班牙和土耳其)的七个多发性硬化症中心招募患者:干预措施:主要结果测量:评估信度(内部一致性、重测和测量误差)和构架效度(结构效度和聚合效度):结果:DTQ、DTSL 和 DIDA-Q 均表现出极佳的重测可靠性[类内相关系数 (95% CI):0.84 (0.80-0.87) 至 0.90 (0.87-0.92)]和内部一致性(Cronbach's α:0.86 至 0.96)。正如假设的那样,这三份问卷之间有很强的相关性,与其他自我报告问卷(感知行走困难、疲劳和害怕跌倒)之间有中等到较强的相关性,与认知信息处理速度、手部灵活性和双任务行走表现(行走与单词表生成任务)之间有低到中等的相关性,显示了趋同效度。DIDA-Q表现出系统的优越性。来自六个不同国家的子集也验证了这些结果。在结构效度分析中,所有问卷都显示出两个主要因素,分别为 "运动驱动 "和 "认知驱动 "子量表:结论:DTQ、DTSL 和 DIDA-Q 具有良好到卓越的测量特性,其中 DIDA-Q 的测量特性最高。在研究和临床实践中,可以使用这些自我报告问卷来评估双重任务困难对行动不便的残疾人日常生活的影响。
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引用次数: 0
Evaluation of Inadequate Response to Ultrasound-Guided Subacromial Corticosteroid Injection in Shoulder Impingement Syndrome: Treatment Failure or Central Sensitization?: Central Sensitization in Injection Response.
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2025.01.469
Büşra Şirin Ahisha, Nurdan Paker, Nur Kesiktaş, Nazlı Derya Buğdayci, Yiğit Can Ahisha

Objective: To evaluate whether central sensitization (CS), pain catastrophizing, and psychological factors are associated with inadequate response to ultrasound-guided subacromial corticosteroid injection (SCI) in patients with chronic shoulder impingement syndrome (SIS).

Design: This study was designed as a prolective observational study, combining analytical cross-sectional and prospective elements to evaluate associations and treatment responses.

Setting: Secondary care outpatient clinic.

Participants: A total of 72 patients aged 18-75 years with SIS and at least 6 months of shoulder pain, planned to undergo ultrasound-guided SCI, were included in the study.

Interventions: Not applicable.

Main outcome measure(s): Treatment response was defined as a ≥50% reduction in pain (VAS) at 4 weeks post-injection. The presence of central sensitization was assessed using the Central Sensitization Inventory (CSI) and Pressure Pain Threshold (PPT) via algometry (ipsilateral deltoid, contralateral deltoid, and contralateral vastus lateralis). Negative thoughts related to pain were evaluated with the Pain Catastrophizing Scale (PCS), and mood status was assessed using the Hospital Anxiety and Depression Scale (HADS).

Results: 48 patients (responders) experienced ≥50% VAS reduction, while 24 (non-responders) did not. Non-responders had significantly higher CSI (p=0.000), HADS-depression (p=0.001), and HADS-anxiety (p=0.000) scores. PPT values were significantly lower in non-responders at ipsilateral deltoid (p=0.030), contralateral deltoid (p=0.045), and contralateral vastus lateralis (p=0.036). CSI was significantly correlated with PPT at ipsilateral deltoid (r=-0.400, p=0.001), contralateral deltoid (r=-0.354, p=0.002), and contralateral vastus lateralis (r=-0.442, p=0.000); PCS total score (r=0.449, p=0.000); HADS-depression score (r=0.572, p=0.000); and HADS-anxiety score (r=0.618, p=0.000). CSI was the most predictive factor for non-response (AUC=0.755, 95% CI: 0.635-0.875). Multivariate analysis identified CSI as an independent predictor (p=0.022), with a predictive accuracy of 72.2%.

Conclusions: Inadequate response to SCI in chronic SIS is strongly associated with CS, psychological distress, and altered pain perception. Integrating CS-targeted interventions into treatment strategies may improve outcomes.

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引用次数: 0
Comparative Efficacy of 5% Dextrose and Corticosteroid Injections in Carpal Tunnel Syndrome: A Systematic Review and Meta-analysis 5% 葡萄糖注射液和皮质类固醇注射液治疗腕管综合征的疗效比较:系统回顾与元分析》。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.07.005
Min Woo Oh MD , Ji-in Park MD , Ga Yang Shim MD, PhD , Hyun-Ho Kong MD, PhD

Objective

This study aims to assess the effectiveness of 5% dextrose (D5W) in comparison to corticosteroids for treating carpal tunnel syndrome (CTS).

Data Sources

A comprehensive systematic search was conducted across MEDLINE (PubMed), Embase, and the Cochrane Central Register of Controlled Trials on November 13, 2023. These were supplemented by manual searches using Google Scholar.

Study Selection

Two independent authors reviewed the literature, resolving any discrepancies through detailed discussions and consultation with a third author.

Data Extraction

Data on primary outcomes (pain assessment) and secondary outcomes (symptom severity and functional status using the Boston Carpal Tunnel Questionnaire, electrophysiologic measures, cross-sectional area, and adverse effects) were extracted independently by the 2 authors (M.W. and H.H.).

Data Synthesis

The analysis included 4 randomized controlled trials and 1 quasi-experimental study, encompassing a total of 212 patients (220 hands) with mild to moderate CTS.

Results

Within 3 months, the D5W injections showed a statistically significant improvement in functional status compared to the corticosteroids with a standard mean difference of −0.34 (95% CI, −0.62 to −0.05). D5W was associated with fewer adverse incidents than corticosteroids (risk ratio, 0.13; 95% CI: 0.03-0.51). No difference was observed between the 2 treatments in other areas.

Conclusions

For patients with mild to moderate CTS, D5W injections were more effective than corticosteroid injections in improving functional status and demonstrated fewer adverse effects. D5W injections also paralleled corticosteroids in pain reduction, symptom severity, electrodiagnostic measures, and cross-sectional area of nerve, recommending D5W as a preferred treatment for mild to moderate CTS.
研究目的本研究旨在评估5%葡萄糖(D5W)与皮质类固醇治疗腕管综合征(CTS)的有效性:数据来源:2023 年 11 月 13 日,在 MEDLINE (PubMed)、Embase 和 Cochrane Central Register of Controlled Trials 中进行了全面的系统检索。此外,还使用谷歌学术(Google Scholar)进行了人工检索:两位独立作者对文献进行了审阅,并通过详细讨论和咨询第三位作者来解决任何差异:两位作者独立提取了主要结果(疼痛评估)和次要结果(使用波士顿腕管问卷调查的症状严重程度和功能状态、电生理测量、横截面积和不良反应)的数据:分析包括 4 项随机对照试验和 1 项准实验研究,共涉及 212 名轻度至中度 CTS 患者(220 只手):3个月内,与皮质类固醇相比,D5W注射剂对功能状态的改善具有统计学意义,标准平均差为-0.34(95%置信区间(CI),-0.62至-0.05)。与皮质类固醇相比,D5W的不良反应较少(风险比为0.13;95% CI为0.03至0.51)。两种疗法在其他方面没有差异:结论:对于轻度至中度 CTS 患者,D5W 注射在改善功能状态方面比皮质类固醇注射更有效,且不良反应更少。在减轻疼痛、症状严重程度、电诊断测量和神经横截面积方面,D5W 注射也与皮质类固醇注射效果相当,因此建议将 D5W 作为轻度至中度 CTS 的首选治疗方法。
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引用次数: 0
Uphill Treadmill Running and Joint Mobilization Improve Dynamic Stability and Ankle Dorsiflexion Range of Motion in Young Adults With Chronic Ankle Instability: A Four-Arm Randomized Controlled Trial 上坡跑步和关节活动可改善慢性踝关节不稳定的年轻成年人的动态稳定性和踝关节外展活动范围:四臂随机对照试验。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.08.025
Yongjie Lao BSc , Zimei Zeng PT, BSc , Zhenni Yu BSc , Yu Gu BSc , Yixiao Jia BSc , Jianxiu Liu PhD , Bing Ruan PT, MSc

Objective

To observe the effect of uphill running and the combined effect of uphill running plus joint mobilizations on dynamic stability and ankle dorsiflexion in young adults with chronic ankle instability (CAI).

Design

Four-arm randomized controlled trial.

Setting

A college rehabilitation center.

Participants

Individuals with CAI (N=73).

Interventions

Participants were randomly assigned to 4 groups: combined uphill running and joint mobilization (URJM), uphill running alone (UR), joint mobilization alone (JM), and control group. The URJM and UR groups received 20-minute running sessions, and the URJM and JM groups received ankle joint mobilizations, all 3 times a week for 4 weeks.

Main Outcome Measures

Cumberland Ankle Instability Tool (CAIT) and Y-balance test (YBT) in anterior, posteromedial (PM), and posterolateral (PL) directions for dynamic stability; weight-bearing lunge test and non-weight-bearing ankle dorsiflexion degree using a goniometer (NWBG) for dorsiflexion.

Results

The UR group showed significant improvements in CAIT, YBT-PL, YBT-PM, and NWBG compared to the control group. The URJM group demonstrated large treatment effects in NWBG compared to both UR and JM groups. Responder analysis indicated that the UR, JM, and URJM groups had a higher likelihood of achieving clinically significant changes (exceeding minimal detectable change or minimal clinically important difference) in CAIT, YBT-PM, YBT-PL, and NWBG compared with the control group. Additionally, the combination of UR and JM was superior to either intervention alone for NWBG, with success rates 1.55 times greater than UR alone and 2.08 times greater than JM alone.

Conclusions

A 4-week UR program improves the subjective feeling of instability, dynamic postural control, and ankle dorsiflexion in young adults with CAI. Compared to UR or JM alone, their combined application can better improve the non-weight-bearing ankle dorsiflexion range of motion.
目的观察上坡跑以及上坡跑加关节活动对慢性踝关节不稳定(CAI)年轻成人的动态稳定性和踝关节外展的综合影响:设计:四臂随机对照试验:参与者:CAI 患者(73 人):参与者被随机分配到四组:联合上坡跑步和关节动员组(URJM)、单独上坡跑步组(UR)、单独关节动员组(JM)和对照组。URJM组和UR组接受20分钟的跑步训练,URJM组和JM组接受踝关节活动,每周三次,共4周:坎伯兰踝关节不稳定性工具(CAIT)和Y-平衡测试(YBT)在前方、后内侧(PM)和后外侧(PL)方向的动态稳定性;负重弓步测试和使用动态关节角度计(NWBG)的非负重踝关节背屈程度:与对照组相比,UR组在CAIT、YBT-PL、YBT-PM和NWBG方面均有明显改善。与 UR 组和 JM 组相比,URJM 组在 NWBG 方面表现出较大的治疗效果。应答者分析表明,与对照组相比,UR、JM 和 URJM 组在 CAIT、YBT-PM、YBT-PL 和 NWBG 方面实现临床显著变化(超过最小可检测变化或最小临床重要差异)的可能性更高。此外,就 NWBG 而言,UR 和 JM 的组合优于单独的干预,成功率是单独 UR 的 1.55 倍,是单独 JM 的 2.08 倍:结论:为期4周的UR项目可改善CAI年轻成人的主观不稳定感、动态姿势控制和踝关节外展。与单独使用 UR 或 JM 相比,两者结合使用能更好地改善非负重踝关节背屈的活动范围。
{"title":"Uphill Treadmill Running and Joint Mobilization Improve Dynamic Stability and Ankle Dorsiflexion Range of Motion in Young Adults With Chronic Ankle Instability: A Four-Arm Randomized Controlled Trial","authors":"Yongjie Lao BSc ,&nbsp;Zimei Zeng PT, BSc ,&nbsp;Zhenni Yu BSc ,&nbsp;Yu Gu BSc ,&nbsp;Yixiao Jia BSc ,&nbsp;Jianxiu Liu PhD ,&nbsp;Bing Ruan PT, MSc","doi":"10.1016/j.apmr.2024.08.025","DOIUrl":"10.1016/j.apmr.2024.08.025","url":null,"abstract":"<div><h3>Objective</h3><div>To observe the effect of uphill running and the combined effect of uphill running plus joint mobilizations on dynamic stability and ankle dorsiflexion in young adults with chronic ankle instability (CAI).</div></div><div><h3>Design</h3><div>Four-arm randomized controlled trial.</div></div><div><h3>Setting</h3><div>A college rehabilitation center.</div></div><div><h3>Participants</h3><div>Individuals with CAI (N=73).</div></div><div><h3>Interventions</h3><div>Participants were randomly assigned to 4 groups: combined uphill running and joint mobilization (URJM), uphill running alone (UR), joint mobilization alone (JM), and control group. The URJM and UR groups received 20-minute running sessions, and the URJM and JM groups received ankle joint mobilizations, all 3 times a week for 4 weeks.</div></div><div><h3>Main Outcome Measures</h3><div>Cumberland Ankle Instability Tool (CAIT) and Y-balance test (YBT) in anterior, posteromedial (PM), and posterolateral (PL) directions for dynamic stability; weight-bearing lunge test and non-weight-bearing ankle dorsiflexion degree using a goniometer (NWBG) for dorsiflexion.</div></div><div><h3>Results</h3><div>The UR group showed significant improvements in CAIT, YBT-PL, YBT-PM, and NWBG compared to the control group. The URJM group demonstrated large treatment effects in NWBG compared to both UR and JM groups. Responder analysis indicated that the UR, JM, and URJM groups had a higher likelihood of achieving clinically significant changes (exceeding minimal detectable change or minimal clinically important difference) in CAIT, YBT-PM, YBT-PL, and NWBG compared with the control group. Additionally, the combination of UR and JM was superior to either intervention alone for NWBG, with success rates 1.55 times greater than UR alone and 2.08 times greater than JM alone.</div></div><div><h3>Conclusions</h3><div>A 4-week UR program improves the subjective feeling of instability, dynamic postural control, and ankle dorsiflexion in young adults with CAI. Compared to UR or JM alone, their combined application can better improve the non-weight-bearing ankle dorsiflexion range of motion.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"106 2","pages":"Pages 177-186"},"PeriodicalIF":3.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142279802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of Aerobic Exercise on Symptom Burden and Quality of Life in Adults With Persisting Post-concussive Symptoms: The ACTBI Randomized Controlled Trial 有氧运动对有持续性脑震荡后症状的成年人的症状负担和生活质量的影响:ACTBI随机临床试验》。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.10.002
Leah J. Mercier PhD , Samantha J. McIntosh BHSc , Chloe Boucher BSc , Julie M. Joyce MSc , Julia Batycky BHSc , Jean-Michel Galarneau PhD , Michael J. Esser MD, PhD , Kathryn J. Schneider PT, PhD , Sean P. Dukelow MD, PhD , Ashley D. Harris PhD , Chantel T. Debert MD, MSc

Objective

To evaluate a 6-week sub-symptom threshold aerobic exercise protocol (AEP) versus a stretching protocol (SP) on symptom burden and quality of life (QoL) in adults with persisting post-concussive symptoms (PPCS).

Design

The Aerobic exercise for treatment of Chronic symptoms following mild Traumatic Brain Injury (ACTBI) Trial was a randomized controlled trial with 2 groups.

Setting

Outpatient brain injury, pain, and physiotherapy clinics.

Participants

A total of 210 participants were screened. A consecutive sample of 52 adults with PPCS and exercise intolerance after mild traumatic brain injury were enrolled. No participants withdrew because of the adverse effects of the intervention.

Interventions

Participants were randomized to a 6-week AEP (n=27) or 6-week SP (n=25).

Main Outcome and Measures

The Rivermead Post Concussion Symptoms Questionnaire was the primary outcome. Secondary outcomes included QoL using the QoL After Brain Injury Questionnaire, in addition to measures of mood, anxiety, functional impact of headache, fatigue, dizziness, exercise tolerance, and sleep.

Results

Participants were a mean (SD) of 43.0 (10.9) years old (75% female) and 24.7 (14.0) months post-injury. In per-protocol analysis, between-group difference (AEP vs SP) was not significant for the Rivermead Post Concussion Symptoms Questionnaire, but QoL After Brain Injury Questionnaire between-group difference was significant (mean change=5.024; 95% Cl, 0.057-9.992; P=.047) from baseline to 6 weeks. In the intention-to-treat analysis, between-group changes in primary and secondary outcomes were not significant.

Conclusions

This trial provides preliminary data to support the prescription of aerobic exercise for adults with PPCS. Despite presenting with exercise intolerance, participants were able to engage in subsymptom threshold exercise with QoL benefits.
目的评估为期6周的症状阈值以下有氧运动方案(AEP)与拉伸方案(SP)对患有持续性脑震荡后症状(PPCS)的成年人的症状负担和生活质量(QoL)的影响:有氧运动治疗轻度脑损伤后慢性症状(ACTBI)试验是一项随机对照试验,分为两组:环境:脑损伤、疼痛和理疗门诊:共筛选了 210 名参与者。连续抽样调查了 52 名轻度脑外伤后患有 PPCS 和运动不耐受的成年人。没有参与者因干预的不良反应而退出:参与者被随机分配到为期6周的AEP(27人)或为期6周的SP(25人):主要结果和测量指标:主要结果是Rivermead脑震荡后症状问卷(RPQ)。次要结果包括使用脑损伤后生活质量问卷(QOLIBRI)进行的QoL,以及情绪、焦虑、头痛的功能影响、疲劳、头晕、运动耐受性和睡眠等方面的测量:参与者平均(标清)43.0(10.9)岁(75%为女性),伤后24.7(14.0)个月。在按方案分析中,RPQ的组间差异(AEP vs SP)不显著,但QOLIBRI从基线到6周的组间差异显著(平均变化=5.024,95% Cl [0.057,9.992],p=0.047)。在意向治疗分析中,主要和次要结果的组间变化不显著:这项试验提供了初步数据,支持为患有 PPCS 的成人开具有氧运动处方。尽管出现了运动不耐受的情况,但参与者仍能进行症状阈值以下的运动,并获得了生活质量方面的益处。
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引用次数: 0
Effects of a 6-Week Treadmill Training With and Without Virtual Reality on Frailty in People With Multiple Sclerosis 有无虚拟现实技术的为期6周的跑步机训练对多发性硬化症患者虚弱程度的影响:多发性硬化症患者的虚弱康复。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.09.010
Tobia Zanotto PhD , Irina Galperin MP , Danya Pradeep Kumar PhD , Anat Mirelman PhD , Shahar Yehezkyahu BPT , Keren Regev MD , Arnon Karni MD , Tanja Schmitz-Hübsch MD , Friedemann Paul MD , Sharon G. Lynch MD , Abiodun E. Akinwuntan PhD , Jianghua He PhD , Bruce R. Troen MD , Hannes Devos PhD , Jeffrey M. Hausdorff PhD , Jacob J. Sosnoff PhD

Objective

To examine the effects of a cognitive-motor rehabilitation program consisting of treadmill training (TT) augmented by virtual reality (TT+VR) on frailty in people with multiple sclerosis (pwMS).

Design

Secondary analysis from a multicenter randomized controlled trial investigating the effects of TT+VR, compared with TT only, on measures of mobility and cognitive function in pwMS.

Setting

Four university research laboratories in 3 countries.

Participants

A total of 124 pwMS were randomized into the parent trial. Here, we studied a subset of n = 83 participants (mean age, 49.4±9.3y; 73.5% female; expanded disability status scale range, 2.0-6.0), who completed the intervention and had complete preintervention and postintervention frailty data.

Interventions

Participants were randomly allocated to TT+VR (n=44) or TT (n=39). Both groups trained 3 times a week for 6 weeks.

Main Outcome Measures

Frailty was assessed using a 40-item frailty index (FI) through standard validated procedures and represented the primary study outcome. Two exploratory frailty indices were also computed by isolating health-related deficits involving the cognitive (FI-physical) or physical (FI-cognitive) domains from the main FI. The assessments were performed at baseline and after 6 weeks, upon intervention completion.

Results

The mean FI of study participants at baseline was 0.33±0.13, indicating a moderate average level of frailty. FI scores improved in both TT+VR and TT groups participants (pooled mean ΔFI, 0.024; 95% CI, 0.010-0.038; F=10.49; P=.002; ηp2=0.115), without any group-by-time interaction (F=0.82; P=.367; ηp2=0.010). However, a significant group-by-time interaction was found for pretraining and posttraining changes in FI-cognitive (F=5.74; P=.019; ηp2=0.066), suggesting a greater improvement for TT+VR group participants than for TT group participants.

Conclusions

TT with or without virtual reality can reduce frailty levels in pwMS. While both TT and TT+VR had a positive effect on overall frailty, only TT+VR improved cognitive aspects of frailty and may represent an appropriate strategy for counteracting frailty in pwMS.
目的研究由虚拟现实技术增强的跑步机训练(TT+VR)组成的认知运动康复项目对多发性硬化症患者(pwMS)虚弱程度的影响:设计:一项多中心随机对照试验的二次分析,该试验调查了TT+VR与仅进行跑步机训练(TT)相比,对多发性硬化症患者活动能力和认知功能的影响:以色列、美国和德国的四所大学研究实验室:共有 124 名 pwMS 被随机纳入母试验。在此,我们研究了83名参与者(平均年龄=49.4±9.3岁,73.5%为女性,EDSS范围=2.0-6.0),他们完成了干预,并拥有干预前后的完整虚弱数据:参与者被随机分配到 TT+VR 组(44 人)或 TT 组(39 人)。两组均每周训练三次,为期六周:通过标准的验证程序,使用 40 项虚弱指数(FI)对虚弱程度进行评估,这也是主要的研究结果。此外,还计算了两个探索性虚弱指数,方法是从主要虚弱指数中分离出与健康相关的认知(FI-体能)或体能(FI-认知)领域的缺陷。评估分别在基线和六周后,即干预完成时进行:研究参与者基线时的平均 FI 为 0.33±0.13,表明平均体弱程度为中等。TT+VR和TT参与者的FI评分均有所改善(汇总平均值ΔFI=0.024,95%CI=0.010-0.038,F=10.49,p=0.002,ηp2=0.115),没有任何组间时间交互作用(F=0.82,p=0.367,ηp2=0.010)。然而,训练前和训练后的 FI 认知变化存在明显的组间时间交互作用(F=5.74,p=0.019,ηp2=0.066),表明 TT+VR 参与者比 TT 参与者有更大的改善:结论:无论有无虚拟现实技术,跑步机训练都能减轻老年人的虚弱程度。虽然 TT 和 TT+VR 对总体虚弱程度都有积极影响,但只有 TT+VR 改善了虚弱程度的认知方面,可能是应对老年肌肉萎缩症患者虚弱程度的适当策略。
{"title":"Effects of a 6-Week Treadmill Training With and Without Virtual Reality on Frailty in People With Multiple Sclerosis","authors":"Tobia Zanotto PhD ,&nbsp;Irina Galperin MP ,&nbsp;Danya Pradeep Kumar PhD ,&nbsp;Anat Mirelman PhD ,&nbsp;Shahar Yehezkyahu BPT ,&nbsp;Keren Regev MD ,&nbsp;Arnon Karni MD ,&nbsp;Tanja Schmitz-Hübsch MD ,&nbsp;Friedemann Paul MD ,&nbsp;Sharon G. Lynch MD ,&nbsp;Abiodun E. Akinwuntan PhD ,&nbsp;Jianghua He PhD ,&nbsp;Bruce R. Troen MD ,&nbsp;Hannes Devos PhD ,&nbsp;Jeffrey M. Hausdorff PhD ,&nbsp;Jacob J. Sosnoff PhD","doi":"10.1016/j.apmr.2024.09.010","DOIUrl":"10.1016/j.apmr.2024.09.010","url":null,"abstract":"<div><h3>Objective</h3><div>To examine the effects of a cognitive-motor rehabilitation program consisting of treadmill training (TT) augmented by virtual reality (TT+VR) on frailty in people with multiple sclerosis (pwMS).</div></div><div><h3>Design</h3><div>Secondary analysis from a multicenter randomized controlled trial investigating the effects of TT+VR, compared with TT only, on measures of mobility and cognitive function in pwMS.</div></div><div><h3>Setting</h3><div>Four university research laboratories in 3 countries.</div></div><div><h3>Participants</h3><div>A total of 124 pwMS were randomized into the parent trial. Here, we studied a subset of n = 83 participants (mean age, 49.4±9.3y; 73.5% female; expanded disability status scale range, 2.0-6.0), who completed the intervention and had complete preintervention and postintervention frailty data.</div></div><div><h3>Interventions</h3><div>Participants were randomly allocated to TT+VR (n=44) or TT (n=39). Both groups trained 3 times a week for 6 weeks.</div></div><div><h3>Main Outcome Measures</h3><div>Frailty was assessed using a 40-item frailty index (FI) through standard validated procedures and represented the primary study outcome. Two exploratory frailty indices were also computed by isolating health-related deficits involving the cognitive (FI-physical) or physical (FI-cognitive) domains from the main FI. The assessments were performed at baseline and after 6 weeks, upon intervention completion.</div></div><div><h3>Results</h3><div>The mean FI of study participants at baseline was 0.33±0.13, indicating a moderate average level of frailty. FI scores improved in both TT+VR and TT groups participants (pooled mean ΔFI, 0.024; 95% CI, 0.010-0.038; F=10.49; <em>P=</em>.002; η<sub>p</sub><sup>2</sup>=0.115), without any group-by-time interaction (F=0.82; <em>P=</em>.367; η<sub>p</sub><sup>2</sup>=0.010<em>)</em>. However, a significant group-by-time interaction was found for pretraining and posttraining changes in FI-cognitive (F=5.74; <em>P=</em>.019; η<sub>p</sub><sup>2</sup>=0.066), suggesting a greater improvement for TT+VR group participants than for TT group participants.</div></div><div><h3>Conclusions</h3><div>TT with or without virtual reality can reduce frailty levels in pwMS. While both TT and TT+VR had a positive effect on overall frailty, only TT+VR improved cognitive aspects of frailty and may represent an appropriate strategy for counteracting frailty in pwMS.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"106 2","pages":"Pages 187-194"},"PeriodicalIF":3.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142340048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Objectively Measured Physical Activity in Children With Developmental Coordination Disorder: A Systematic Review and Meta-analysis 客观测量发育协调障碍儿童的体育活动量:系统回顾与元分析》。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.06.002
Huynh-Truc Tran MS , Wen-Chao Ho PhD , Li-Wei Chou PhD , Yao-Chuen Li PhD

Objective

To conduct a systematic review and meta-analysis to understand the difference in objectively measured physical activities (PAs) between children with and without developmental coordination disorder (DCD).

Data Sources

A systematic literature search of 4 databases (PubMed, Science Direct, Web of Science, and Cochrane library) was conducted in July 2023.

Study Selection

Studies that met the following criteria were considered classified children with DCD based on Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV), DSM-IV-Text Revision, or DSM-V diagnosis criteria, evaluated PA using objective measurements and provided the amount of time spent in PA and/or sedentary behavior, included a control group of typically developing children, and written in English.

Data Extraction

Data extracted from all included studies were: first author's surname and publication year, study design, country, total sample size, the measure of PA, the intensity of PA, categories of PA level, and main finding(s).

Data Synthesis

Twelve articles met the inclusion criteria for the systematic review, 10 of which were included in the meta-analysis. The overall mean difference in moderate-to-vigorous PA (MVPA) between 2 groups was −0.17 (95% CI, −0.25 to −0.09), (I2=48.7%, P=.029). A subgroup analysis by age (ie, school-aged vs. preschool) showed a significant pooled effect size with no heterogeneity in school-aged children (ie, 6-14y) (standardized mean difference=−0.27, 95% CI, −0.38 to −0.16, I2=43.1%, P=.08).

Conclusions

Children with DCD spent significantly less time participating in MVPA, particularly those aged between 6 and 14 years. These findings highlight the need for increased awareness among parents and physicians regarding insufficient participation in PA among children with DCD.
目的进行系统回顾和荟萃分析,以了解发育协调障碍(DCD)儿童与非发育协调障碍儿童在客观测量的体育活动(PA)方面的差异:数据来源:2023 年 7 月,对四个数据库(PubMed、Science Direct、Web of Science 和 Cochrane 图书馆)进行了系统性文献检索:符合以下标准的研究均被考虑在内:(1)研究应根据 DSM-IV、DSM-IV-TR 或 DSM-V 诊断标准对患有 DCD 的儿童进行分类;(2)研究旨在使用客观测量方法对 PA 进行评估,并提供 PA 和/或 SB 所花费的时间;(3)招募了 TD 儿童作为对照组;(4)全文以英语撰写:数据综合:12 篇文章符合系统综述的纳入标准,其中 10 篇进入荟萃分析。两组中度至剧烈运动强度(MVPA)的总体平均差异为-0.17(95% CI:-0.25 至 -0.09,I2 = 48.7%,P = 0.029)。在进一步进行年龄分组分析时(即学龄儿童与学龄前儿童),发现学龄儿童(即 6-14 岁儿童)的集合效应大小显著,且无异质性(标准化平均差异 (SMD) = -0.27,95% CI:-0.38 至 -0.16,I2 = 43.1%,p = 0.08):结论:患有多动症的儿童参加 MVPA 的时间明显较少,尤其是年龄在 6 岁至 14 岁之间的儿童。这些发现有助于提高家长和医生对残疾儿童参与体育锻炼不足的认识。
{"title":"Objectively Measured Physical Activity in Children With Developmental Coordination Disorder: A Systematic Review and Meta-analysis","authors":"Huynh-Truc Tran MS ,&nbsp;Wen-Chao Ho PhD ,&nbsp;Li-Wei Chou PhD ,&nbsp;Yao-Chuen Li PhD","doi":"10.1016/j.apmr.2024.06.002","DOIUrl":"10.1016/j.apmr.2024.06.002","url":null,"abstract":"<div><h3>Objective</h3><div>To conduct a systematic review and meta-analysis to understand the difference in objectively measured physical activities (PAs) between children with and without developmental coordination disorder (DCD).</div></div><div><h3>Data Sources</h3><div>A systematic literature search of 4 databases (PubMed, Science Direct, Web of Science, and Cochrane library) was conducted in July 2023.</div></div><div><h3>Study Selection</h3><div><span>Studies that met the following criteria were considered classified children with DCD based on </span><em>Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition</em> (DSM-IV), DSM-IV-Text Revision, or DSM-V diagnosis criteria, evaluated PA using objective measurements and provided the amount of time spent in PA and/or sedentary behavior, included a control group of typically developing children, and written in English.</div></div><div><h3>Data Extraction</h3><div>Data extracted from all included studies were: first author's surname and publication year, study design, country, total sample size, the measure of PA, the intensity of PA, categories of PA level, and main finding(s).</div></div><div><h3>Data Synthesis</h3><div>Twelve articles met the inclusion criteria for the systematic review, 10 of which were included in the meta-analysis. The overall mean difference in moderate-to-vigorous PA (MVPA) between 2 groups was −0.17 (95% CI, −0.25 to −0.09), (<em>I</em><sup>2</sup>=48.7%, <em>P</em>=.029). A subgroup analysis by age (ie, school-aged vs. preschool) showed a significant pooled effect size with no heterogeneity in school-aged children (ie, 6-14y) (standardized mean difference=−0.27, 95% CI, −0.38 to −0.16, <em>I</em><sup>2</sup>=43.1%, <em>P</em>=.08).</div></div><div><h3>Conclusions</h3><div>Children with DCD spent significantly less time participating in MVPA, particularly those aged between 6 and 14 years. These findings highlight the need for increased awareness among parents and physicians regarding insufficient participation in PA among children with DCD.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"106 2","pages":"Pages 269-279"},"PeriodicalIF":3.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141431233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Risk Factors for Falls Among Hospitalized Medical Patients – A Systematic Review and Meta-analysis 住院病人跌倒的风险因素--系统回顾与荟萃分析。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.06.015
Jeannelle Heinzmann MB , Michael L. Rossen MMed , Orestis Efthimiou PhD , Christine Baumgartner MD, MSc , Maria M. Wertli MD, PhD , Nicolas Rodondi MD, MAS , Carole E. Aubert MD, MSc , Fabian D. Liechti MD, PhD

Objective

To identify and quantify risk factors for in-hospital falls in medical patients.

Data Sources

Six databases (MEDLINE, Embase, Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, CINAHL, and Google Scholar) were systematically screened until April 11, 2023, to identify relevant articles.

Study Selection

All titles and abstracts of the retrieved articles were independently screened by 2 researchers who also read the full texts of the remaining articles. Quantitative studies that assessed risk factors for falls among adult patients acutely hospitalized were included in the review. Publications that did not capture internal medicine patients or focused on other specific populations were excluded.

Data Extraction

Information on study characteristics and potential risk factors were systematically extracted. Risk of bias was assessed using the Quality in Prognosis Studies tool. Preferred Reporting Items for Systematic Reviews and Meta-Analyses and Meta-analyses of Observational Studies in Epidemiology guidelines were followed for reporting.

Data Synthesis

The main outcome was any in-hospital falls. Using a random-effects meta-analysis model, association measures for each risk factor reported in 5 or more studies were pooled. Separate analyses according to effect measure and studies adjusted for sex and age at least were performed. Of 5067 records retrieved, 119 original publications from 25 countries were included. In conclusion, 23 potential risk factors were meta-analyzed. Strong evidence with large effect sizes was found for a history of falls (odds ratio [OR], 2.54; 95% confidence interval [CI], 1.63-3.96; I2, 91%), antidepressants (pooled OR, 2.25; 95% CI, 1.92-2.65; I2, 0%), benzodiazepines (OR, 1.97; 95% CI, 1.68-2.31; I2, 0%), hypnotics–sedatives (OR, 1.90; 95% CI, 1.53-2.36; I2, 46%), and antipsychotics (OR, 1.61; 95% CI, 1.33-1.95; I2, 0%). Furthermore, evidence of associations with male sex (OR, 1.22, 95% CI, 0.99-1.50; I2, 65%) and age (OR, 1.17, 95% CI, 1.02-1.35; I2, 72%) were found, but effect sizes were small.

Conclusions

The comprehensive list of risk factors, which specifies the strength of evidence and effect sizes, could assist in the prioritization of preventive measures and interventions.
目的:确定并量化内科病人院内跌倒的风险因素:识别并量化内科病人院内跌倒的风险因素:截至 2023 年 4 月 11 日,对六个数据库(MEDLINE、Embase、Cochrane 系统综述数据库、Cochrane 对照试验中央注册库、CINAHL 和 Google Scholar)进行了系统筛选,以确定相关文章:所有检索文章的标题和摘要均由两名研究人员独立筛选,他们还阅读了其余文章的全文。综述包括评估急性住院成年患者跌倒风险因素的定量研究。数据提取:数据提取:系统地提取研究特征和潜在风险因素的相关信息。使用预后研究质量(QUIPS)工具评估偏倚风险。报告遵循 PRISMA 和 MOOSE 指南:主要结果为院内跌倒。采用随机效应荟萃分析模型,对五项或五项以上研究中报告的每个风险因素的关联测量值进行汇总。根据效应指标和至少对性别和年龄进行调整的研究分别进行分析。在检索到的 5,067 条记录中,纳入了来自 25 个国家的 119 篇原始出版物。最后,对 23 个潜在风险因素进行了元分析。研究发现,有跌倒史(OR 2.54;95% 置信区间 [95% CI] 1.63-3.96;I2 91%)、抗抑郁药(汇总 OR 2.25;95% 置信区间 [95% CI] 1.92-2.65;I2 0%)、苯二氮卓类(OR 1.97;95% CI 1.68-2.31;I2 0%)、催眠药-镇静剂(OR 1.90;95% CI 1.53-2.36;I2 46%)和抗精神病药(OR 1.61;95% CI 1.33-1.95;I2 0%)。此外,还发现了与男性性别(OR 1.22,95% CI 0.99-1.50,I2 65%)和年龄(OR 1.17,95% CI 1.02-1.35,I2 72%)相关的证据,但效应大小很小:综合风险因素清单明确了证据强度和效应大小,有助于确定预防措施和干预措施的优先次序。
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引用次数: 0
Development and External Validation of a Motor Intention–Integrated Prediction Model for Upper Extremity Motor Recovery After Intention-Driven Robotic Hand Training for Chronic Stroke 慢性中风意向驱动机器人手训练后上肢运动恢复的运动意向综合预测模型的开发和外部验证
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.08.015
Chengpeng Hu MSc , Chun Hang Eden Ti PhD , Xiangqian Shi MSc , Kai Yuan PhD , Thomas W.H. Leung MD , Raymond Kai-Yu Tong PhD

Objective

To derive and validate a prediction model for minimal clinically important differences (MCIDs) in upper extremity (UE) motor function after intention-driven robotic hand training using residual voluntary electromyography (EMG) signals from affected UE.

Design

A prospective longitudinal multicenter cohort study. We collected preintervention candidate predictors: demographics, clinical characteristics, Fugl-Meyer assessment of UE (FMAUE), Action Research Arm Test scores, and motor intention of flexor digitorum and extensor digitorum (ED) measured by EMG during maximal voluntary contraction (MVC). For EMG measures, recognizing challenges for stroke survivors to move paralyzed hand, peak signals were extracted from 8 time windows during MVC-EMG (0.1-5s) to identify subjects’ motor intention. Classification and regression tree algorithm was employed to predict survivors with MCID of FMAUE. Relationship between predictors and motor improvements was further investigated.

Setting

Nine rehabilitation centers.

Participants

Chronic stroke survivors (N=131), including 87 for derivation sample, and 44 for validation sample.

Interventions

All participants underwent 20-session robotic hand training (40min/session, 3-5sessions/wk).

Main Outcome Measures

Prediction efficacies of models were assessed by area under the receiver operating characteristic curve (AUC). The best effective model was final model and validated using AUC and overall accuracy.

Results

The best model comprised FMAUE (cutoff score, 46) and peak activity of ED from 1-second MVC-EMG (MVC-EMG 4.604 times higher than resting EMG), which demonstrated significantly higher prediction accuracy (AUC, 0.807) than other time windows or solely using clinical scores (AUC, 0.595). In external validation, this model displayed robust prediction (AUC, 0.916). Significant quadratic relationship was observed between ED-EMG and FMAUE increases.

Conclusions

This study presents a prediction model for intention-driven robotic hand training in chronic stroke survivors. It highlights significance of capturing motor intention through 1-second EMG window as a predictor for MCID improvement in UE motor function after 20-session robotic training. Survivors in 2 conditions showed high percentage of clinical motor improvement: moderate-to-high motor intention and low-to-moderate function; as well as high intention and high function.
目的:利用受影响上肢的残余自主肌电信号,推导并验证意向驱动机械手训练后上肢运动功能最小临床重要差异(MCID)的预测模型:设计:一项前瞻性纵向多中心队列研究。我们收集了干预前的候选预测因素:人口统计学、临床特征、Fugl-Meyer UE 评估(FMAUE)、行动研究手臂测试评分,以及最大自主收缩(MVC)时通过肌电图测量的屈指肌和伸指肌(ED)的运动意向。在肌电图测量中,考虑到中风幸存者在移动瘫痪手时面临的挑战,我们从最大自主收缩过程中的八个时间窗口(0.1 秒至 5 秒)中提取峰值信号,以识别受试者的运动意向。采用分类和回归树算法预测幸存者的运动意向,MCID 为 FMAUE。进一步研究了预测因子与运动改善之间的关系:九个康复中心:慢性中风幸存者(131 人),其中 87 人为推导样本,44 人为验证样本:干预措施:所有参与者接受 20 次机器人手训练(40 分钟/次,3-5 次/周):通过接收者操作特征曲线下面积(AUC)评估模型的预测效果。最佳有效模型为最终模型,并通过AUC和总体准确性进行验证:最佳模型由 FMAUE(截断分数:46)和一秒 MVC-EMG 的 ED 峰值活动(MVC-EMG 比静息-EMG 高 4.604 倍)组成,其预测准确率(AUC:0.807)明显高于其他时间窗口或仅使用临床评分(AUC:0.595)。在外部验证中,该模型显示出强大的预测能力(AUC:0.916)。在 ED-EMG 和 FMAUE 的增加之间观察到了显著的二次关系:本研究提出了慢性中风幸存者意向驱动机器人手训练的预测模型。它强调了通过 1 秒肌电图窗口捕捉运动意向作为 20 次机器人训练后 UE 运动功能 MCID 改善的预测因子的重要性。在两种情况下,幸存者的临床运动改善比例较高:中度至高度运动意向和低度至中度功能;以及高度意向和高度功能。
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引用次数: 0
Factors Related to the Quality and Stability of Partner Relationships After Stroke: A Systematic Literature Review 与中风后伴侣关系的质量和稳定性有关的因素:系统性文献综述。
IF 3.6 2区 医学 Q1 REHABILITATION Pub Date : 2025-02-01 DOI: 10.1016/j.apmr.2024.05.016
Brenda van den Broek MA , Laura Verrijt MSc , Sophie Rijnen PhD , Caroline van Heugten PhD , Boudewijn Bus MD, PhD

Objective

To provide an overview of the current state of knowledge on factors related to relationship quality and relationship stability after stroke.

Data Sources

Cumulative Index to Nursing and Allied Health (CINAHL), Embase, MEDLINE, Psychology and Behavioral Sciences Collection, APA PsycINFO, and PubMed were searched on November 15, 2022, for literature on factors associated with (1) relation quality and (2) relation stability after stroke.

Study Selection

English quantitative and qualitative studies investigating factors associated with relation quality and/or stability after stroke were included. Three reviewers independently assessed eligibility. Consensus meetings were held in case of divergent opinions. A total of 44 studies were included.

Data Extraction

Information regarding study objectives and characteristics, participant demographics, independent and dependent variables, and main findings was extracted. Study quality was rated using the Joanna Briggs Institute Checklist for Analytical Cross-Sectional Studies and/or the Critical Appraisal Skills Programme Checklist for Qualitative Research. Both were administered by the lead reviewer and checked by the second reviewer. Identified factors are described and presented according to the domains of the International Classification of Functioning, Disability, and Health model.

Data Synthesis

Thirty-seven factors related to relationship quality after stroke were identified, covering the domains of body functions and structures (eg, cognitive problems), activities (eg, decrease in physical intimacy), participation (eg, being socially active), environment (eg, medication side effects), and personal factors (eg, hypervigilance). Eight factors related to relationship stability were identified, covering the domains of participation (agreement on reciprocal roles) and personal factors (eg, quality of prestroke relation).

Conclusions

Relationship quality and stability after stroke are related to a multitude of factors. Future research should confirm the relevance of factors found in a few studies of suboptimal quality; explore possible associations between relationship stability and factors falling in the domains of body functions and structure, activity, and environmental factors; and explicitly explore potential positive effects of stroke on relationships.
目的概述与中风后关系质量和关系稳定性相关因素的知识现状:2022 年 11 月 15 日,检索了 Cumulative Index to Nursing and Allied Health、Embase、MEDLINE、Psychology and Behavioral Sciences Collection、APA PsycINFO 和 PubMed,以查找有关中风后(1)关系质量和(2)关系稳定性相关因素的文献:研究筛选:纳入调查中风后关系质量和/或稳定性相关因素的英文定量和定性研究。三位审稿人独立评估研究资格。如有不同意见,则召开共识会议。共纳入 44 项研究:提取了有关研究目标和特征、参与者人口统计学特征、自变量和因变量以及主要研究结果的信息。研究质量采用 JBI 分析性横断面研究核对表和/或 CASP 定性研究核对表进行评定。这两项工作均由首席审稿人完成,并由第二位审稿人检查。确定的因素根据国际功能、残疾和健康分类模型的领域进行描述和呈现:确定了 37 个与脑卒中后关系质量相关的因素,涵盖身体功能和结构(如认知问题)、活动(如身体亲密程度下降)、参与(如积极参与社交活动)、环境(如药物副作用)和个人因素(如过度警觉)等领域。与人际关系稳定性相关的 8 个因素涵盖了参与(就互惠角色达成一致)和个人因素(如中风前人际关系的质量):结论:中风后的关系质量和稳定性与多种因素有关。未来的研究应确认在少数质量不佳的研究中发现的因素的相关性,探索关系稳定性与身体功能和结构、活动和环境因素领域中的因素之间可能存在的关联,并明确探索中风对关系的潜在积极影响。
{"title":"Factors Related to the Quality and Stability of Partner Relationships After Stroke: A Systematic Literature Review","authors":"Brenda van den Broek MA ,&nbsp;Laura Verrijt MSc ,&nbsp;Sophie Rijnen PhD ,&nbsp;Caroline van Heugten PhD ,&nbsp;Boudewijn Bus MD, PhD","doi":"10.1016/j.apmr.2024.05.016","DOIUrl":"10.1016/j.apmr.2024.05.016","url":null,"abstract":"<div><h3>Objective</h3><div>To provide an overview of the current state of knowledge on factors related to relationship quality and relationship stability after stroke.</div></div><div><h3>Data Sources</h3><div>Cumulative Index to Nursing and Allied Health (CINAHL), Embase, MEDLINE, Psychology and Behavioral Sciences Collection, APA PsycINFO, and PubMed were searched on November 15, 2022, for literature on factors associated with (1) relation quality and (2) relation stability after stroke.</div></div><div><h3>Study Selection</h3><div>English quantitative and qualitative studies investigating factors associated with relation quality and/or stability after stroke were included. Three reviewers independently assessed eligibility. Consensus meetings were held in case of divergent opinions. A total of 44 studies were included.</div></div><div><h3>Data Extraction</h3><div>Information regarding study objectives and characteristics, participant demographics, independent and dependent variables, and main findings was extracted. Study quality was rated using the Joanna Briggs Institute Checklist for Analytical Cross-Sectional Studies and/or the Critical Appraisal Skills Programme Checklist for Qualitative Research. Both were administered by the lead reviewer and checked by the second reviewer. Identified factors are described and presented according to the domains of the International Classification of Functioning, Disability, and Health model.</div></div><div><h3>Data Synthesis</h3><div>Thirty-seven factors related to relationship quality after stroke were identified, covering the domains of body functions and structures (eg, cognitive problems), activities (eg, decrease in physical intimacy), participation (eg, being socially active), environment (eg, medication side effects), and personal factors (eg, hypervigilance). Eight factors related to relationship stability were identified, covering the domains of participation (agreement on reciprocal roles) and personal factors (eg, quality of prestroke relation).</div></div><div><h3>Conclusions</h3><div>Relationship quality and stability after stroke are related to a multitude of factors. Future research should confirm the relevance of factors found in a few studies of suboptimal quality; explore possible associations between relationship stability and factors falling in the domains of body functions and structure, activity, and environmental factors; and explicitly explore potential positive effects of stroke on relationships.</div></div>","PeriodicalId":8313,"journal":{"name":"Archives of physical medicine and rehabilitation","volume":"106 2","pages":"Pages 255-268"},"PeriodicalIF":3.6,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141079977","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Archives of physical medicine and rehabilitation
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