Time and Motion Studies

时间与运动研究
  • 文章类型: Journal Article
    背景:幼儿龋齿(ECC)是影响数百万儿童的重大全球健康问题。缓解这一问题需要来自可靠的监视系统的最新信息。这使基于证据的决策能够制定口腔健康政策。世界卫生组织(WHO)提倡在口腔疾病监测中采用移动技术,因为它们的效率和易于应用。该研究描述了开发一种电子,埃及学龄前儿童口腔健康监测系统(EOHSS),使用地区卫生信息系统(DHIS2)开源平台及其Android应用程序,并评估其在数据采集中的可行性。
    方法:为DHIS2TrackerAndroidCapture应用程序配置了DHIS2服务器,以允许个人级别的数据输入。根据世卫组织2030年行动计划选择了EOHSS指标。基于临床数据捕获开发了两种用于EOHSS的模式:面对面和远程/异步。试点团队中的八名牙医使用特定于模态的电子设备收集了214个事件。飞行员团队的反馈是关于EOHSS在收集数据方面的可行性,我们进行了时间-运动研究,以评估两周内的工作流程.采用独立t检验和统计过程控制技术进行数据分析。
    结果:试验小组报告了对EOHSS结构的积极反馈。在从儿童获取临床数据之前,通过收集护理人员的数据来调整工作流程以确定监测任务的优先级,以提高工作效率。与远程模拟(5.1±0.9分钟)相比,面对面模式(4.2±0.7分钟)需要更短的数据捕获时间。p<0.001)。临床数据的采集占两种模式所需时间的16.9%和21.1%,分别。面对面模态所需的时间表现出随机变化,远程模态任务显示出执行任务的时间减少的趋势。
    结论:DHIS2为开发电子,口腔健康监测系统。与面对面相比,远程数据的数据捕获时间相差一分钟,这表明尽管耗时略多,远程医疗仍然显示出远程口腔健康评估的希望,这在牙科专业人员有限的地区特别有价值。有可能扩大口腔健康筛查计划的范围。
    BACKGROUND: Early childhood caries (ECC) is a major global health issue affecting millions of children. Mitigating this problem requires up-to-date information from reliable surveillance systems. This enables evidence-based decision-making to devise oral health policies. The World Health Organization (WHO) advocates the adoption of mobile technologies in oral disease surveillance because of their efficiency and ease of application. The study describes developing an electronic, oral health surveillance system (EOHSS) for preschoolers in Egypt, using the District Health Information System (DHIS2) open-source platform along with its Android App, and assesses its feasibility in data acquisition.
    METHODS: The DHIS2 Server was configured for the DHIS2 Tracker Android Capture App to allow individual-level data entry. The EOHSS indicators were selected in line with the WHO Action Plan 2030. Two modalities for the EOHSS were developed based on clinical data capture: face-to-face and tele/asynchronous. Eight dentists in the pilot team collected 214 events using modality-specific electronic devices. The pilot\'s team\'s feedback was obtained regarding the EOHSS\'s feasibility in collecting data, and a time-motion study was conducted to assess workflow over two weeks. Independent t-test and Statistical Process Control techniques were used for data analysis.
    RESULTS: The pilot team reported positive feedback on the structure of the EOHSS. Workflow adaptations were made to prioritize surveillance tasks by collecting data from caregivers before acquiring clinical data from children to improve work efficiency. A shorter data capture time was required during face-to-face modality (4.2 ± 0.7 min) compared to telemodality (5.1 ± 0.9 min), p < 0.001). The acquisition of clinical data accounted for 16.9% and 21.1% of the time needed for both modalities, respectively. The time required by the face-to-face modality showed random variation, and the tele-modality tasks showed a reduced time trend to perform tasks.
    CONCLUSIONS: The DHIS2 provides a feasible solution for developing electronic, oral health surveillance systems. The one-minute difference in data capture time in telemodality compared to face-to-face indicates that despite being slightly more time-consuming, telemodality still shows promise for remote oral health assessments that is particularly valuable in areas with limited access to dental professionals, potentially expanding the reach of oral health screening programs.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    目的:本研究比较了准备时间,错误,满意,在一项随机研究中,与两种需要重建的RSV疫苗(VRR1和VRR2)相比,单盲时间和运动研究。方法:药剂师,护士,和药学技术人员被随机分配到三种疫苗的制备顺序。参与者阅读说明,然后连续制备三种疫苗,其间有3至5分钟的洗脱期。由训练有素的药剂师对准备时间和错误进行视频记录和审查,使用预定义,疫苗特异性检查表。参与者的人口统计,对疫苗制备的满意度,并记录疫苗偏好。受试者内方差分析用于比较准备时间。混合效应泊松和有序逻辑回归模型用于比较准备错误的数量和满意度得分,分别。结果:63名药师(60%),护士(35%)和药学技术人员(5%)参加了美国四个地点的活动。PFS的每个剂量的最小二乘平均准备时间比VRR1快141.8秒(95%CI:156.8,126.7;p<0.0001),比VRR2快103.6秒(118.7,88.5;p<0.0001),比合并的VRR快122.7秒(95%CI:134.2,111.2;p<0.0001)。PFS的总体满意度(“非常”和“非常”)为87.3%,VRR1为28.6%,VRR2为47.6%。大多数参与者(81.0%)更喜欢PFS疫苗。局限性:这项研究由于无法完全失明的观察者而受到限制。为了尽量减少秩序的影响,我们使用了3序列块设计,然而,疫苗的制备顺序可能影响结局.参与者被评估一次,而如果进行重复制备,则每种疫苗的训练效率可能会提高。结论:PFS疫苗可以大大简化疫苗制备过程,允许管理员每小时准备的剂量几乎是小瓶和注射器系统的四倍。
    UNASSIGNED: The current study compared preparation time, errors, satisfaction, and preference for a prefilled syringe (PFS) versus two RSV vaccines requiring reconstitution (VRR1 and VRR2) in a randomized, single-blinded time and motion study.
    UNASSIGNED: Pharmacists, nurses, and pharmacy technicians were randomized to a preparation sequence of the three vaccines. Participants read instructions, then consecutively prepared the three vaccines with a 3-5-min washout period in between. Preparations were video recorded and reviewed by a trained pharmacist for preparation time and errors using predefined, vaccine-specific checklists. Participant demographics, satisfaction with vaccine preparation, and vaccine preference were recorded. Within-subjects analysis of variance was used to compare preparation time. Mixed-effects Poisson and ordered logistic regression models were used to compare the number of preparation errors and satisfaction scores, respectively.
    UNASSIGNED: Sixty-three pharmacists (60%), nurses (35%), and pharmacy technicians (5%) participated at four sites in the United States. The least squares mean preparation time per dose for PFS was 141.8 s (95% CI = 156.8-126.7; p <.0001) faster than for VRR1, 103.6 s (95% CI = 118.7-88.5; p <.0001) faster than for VRR2, and 122.7 s (95% CI = 134.2-111.2; p <.0001) faster than the pooled VRRs. Overall satisfaction (combined \"Very\" and \"Extremely\") was 87.3% for PFS, 28.6% for VRR1, and 47.6% for VRR2. Most participants (81.0%) preferred the PFS vaccine.
    UNASSIGNED: The study is limited by the inability to completely blind observers. To minimize the effects of order, we utilized a 3-sequence block design; however, the order in which the vaccines were prepared may have affected outcomes. Participants were assessed once, whereas if repeated preparations were performed there may have been trained efficiencies gained for each vaccine.
    UNASSIGNED: PFS vaccines can greatly simplify the vaccine preparation process, allowing administrators to prepare almost four times more doses per hour than with vial and syringe systems.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    背景:Eswatini在提供糖尿病和高血压治疗方面面临着持续的挑战,医护人员短缺加剧了。实施旨在解决这些问题的WHO-PEN干预措施,然而,它们对医护人员时间要求和相关成本的影响仍不清楚.
    方法:这项研究采用了时间和运动分析和自下而上的成本评估,以量化在埃斯瓦蒂尼全国范围内扩大WHO-PEN干预措施所需的人力和财政资源。
    结果:研究结果表明,与控制臂诊所相比,干预臂诊所的医护人员报告的工作日持续时间更长,然而每个患者花费的时间更少,而看更多的患者。世卫组织-PEN干预措施的实施增加了医护人员的工作量,但也导致患者护理利用率显着增加。此外,确定了患者就诊的早晨高峰,建议优化患者流量的潜在机会。值得注意的是,通过WHO-PEN干预措施在全国范围内扩大护理提供被证明比扩大护理标准治疗更节约成本。
    结论:WHO-PEN干预措施有望改善Eswatini的糖尿病和高血压治疗,同时提供有效的解决方案。然而,解决医疗保健劳动力创建和保留方面的挑战对于持续有效至关重要。政策制定者必须考虑世卫组织-PEN干预措施的所有方面,以便做出知情决策。试验注册美国临床试验注册中心。NCT04183413。试用注册日期:2019年12月3日。https://ichgcp.net/clinical-trials-registry/NCT04183413。
    BACKGROUND: Eswatini faces persistent challenges in providing care for diabetes and hypertension, exacerbated by a shortage of healthcare workers. The implementation of WHO-PEN interventions aimed to address these issues, yet their effects on healthcare worker time requirements and associated costs remain unclear.
    METHODS: This study employed a time-and-motion analysis and a bottom-up cost assessment to quantify the human and financial resources required for scaling up WHO-PEN interventions nationally in Eswatini for all estimated diabetic and hypertensive patients.
    RESULTS: Findings reveal that healthcare workers in intervention-arm clinics reported longer workday durations compared to those in control-arm clinics, yet spent less time per patient while seeing more patients. The implementation of WHO-PEN interventions increased the workload on healthcare workers but also led to a notable increase in patient care utilization. Furthermore, a morning peak in patient visits was identified, suggesting potential opportunities for optimizing patient flow. Notably, scaling up care provision nationally with WHO-PEN interventions proved to be more cost saving than expanding standard-of-care treatment.
    CONCLUSIONS: WHO-PEN interventions hold promise in improving access to diabetes and hypertension care in Eswatini while offering an efficient solution. However, addressing challenges in healthcare workforce creation and retention is crucial for sustained effectiveness. Policy makers must consider all aspects of the WHO-PEN intervention for informed decision-making. Trial registration US Clinical Trials Registry. NCT04183413. Trial registration date: December 3, 2019. https://ichgcp.net/clinical-trials-registry/NCT04183413.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:初级卫生保健(PHC)中口腔卫生人力的有效规划对于确保社区公平获得服务至关重要。这需要对人口的需求进行细致的检查,口腔健康专业人员的战略分配,和有效的人力资源管理。在这种情况下,为满足用户/家庭/社区的需求而花费在护理上的平均时间是医疗保健专业劳动力规划方法的核心变量。然而,许多时间指标完全基于专业判断或经验。
    目的:计算口腔健康小组在初级卫生保健中进行的活动的平均时间参数。
    方法:这是一项描述性观察性研究,使用时间运动方法在圣保罗市的五个初级卫生保健单位进行,SP,巴西。在典型工作周的五天内,对口腔健康团队成员进行了40小时的直接连续观察。
    结果:12名牙医共进行了696.05小时的观察,三个口腔健康助理,和五个口腔健康技术员.牙医的主要活动是咨询,平均持续时间为24.39分钟,占用了他们工作时间的42.36%,其次是文件,占12.15%。口腔健康助理将31.57%的时间用于感染控制,而口腔健康技术人员在文档上花费了22.37%。
    结论:该研究为牙科护理团队开展的活动建立了时间标准,并为员工计划方法的应用提供了支持,以审查和优化工作流程和公共政策。
    BACKGROUND: Efficient planning of the oral health workforce in Primary Health Care (PHC) is paramount to ensure equitable community access to services. This requires a meticulous examination of the population\'s needs, strategic distribution of oral health professionals, and effective human resource management. In this context, the average time spent on care to meet the needs of users/families/communities is the central variable in healthcare professional workforce planning methods. However, many time measures are solely based on professional judgment or experience.
    OBJECTIVE: Calculate the average time parameters for the activities carried out by the oral health team in primary health care.
    METHODS: This is a descriptive observational study using the time-motion method carried out in five Primary Health Care Units in the city of São Paulo, SP, Brazil. Direct and continuous observation of oral health team members occurred for 40 h spread over five days of a typical work week.
    RESULTS: A total of 696.05 h of observation were conducted with 12 Dentists, three Oral Health Assistants, and five Oral Health Technicians. The Dentists\' main activity was consultation with an average duration of 24.39 min, which took up 42.36% of their working time, followed by documentation with 12.15%. Oral Health Assistants spent 31.57% of their time on infection control, while Oral Health Technicians spent 22.37% on documentation.
    CONCLUSIONS: The study establishes time standards for the activities performed by the dental care team and provides support for the application of workforce planning methods that allow for review and optimization of the work process and public policies.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Randomized Controlled Trial
    髌股疼痛综合征(PFPS)是一组对个体日常生活活动产生负面影响的症状,导致功能性残疾和大量劳动力损失,尤其是年轻人。PFPS通常是由于股内侧斜肌(VMO)的虚弱导致the骨跟踪异常和疼痛。我们的研究旨在比较高强度激光治疗(HILT)对不同电物理药物(EPA)治疗PFPS的疼痛和下肢功能的疗效。该研究设计为单盲随机对照试验。45名PFPS患者(25-45岁)被纳入研究。将患者随机分为3组,共治疗10次,疗程2周,一周五天。第1组采用高强度激光(HILT)和运动程序。超声(美国),经皮神经电刺激(TENS),并将锻炼计划应用于第2组。在第3组,美国,干扰电流(IFC),并应用了锻炼计划。两组都进行了三项评估:治疗前,治疗后,治疗后12周。结果测量包括疼痛严重程度的视觉模拟量表(VAS),膝关节屈曲运动范围(FROM),Q角,痛阈值,股四头肌和腿筋的肌肉力量,Kujala髌股评分,下肢功能量表(LEFS),和定时和去测试(TUG)。方差分析用于比较各组数据,在干预前和干预后第3个月使用双向重复测量ANOVA进行比较.LSD和Bonferroni事后检验也用于鉴定组间差异。第2组和第3组在疼痛和功能方面具有统计学上的有效性(p<0.05)。发现第1组在减轻疼痛方面比其他组在统计学上更有效(95%置信区间(CI),0.000/0.000;p=0.000),增加膝关节屈曲角度(95%CI,127.524/135.809;p=0.000),增加下肢功能(95%CI,75.970/79.362;p=0.000)。这项研究表明,与US-TENS组合和US-干扰目前的联合治疗相比,高强度激光治疗在随访3个月后被发现是治疗髌股疼痛综合征的更有效方法。此外,HILT可作为一种有效的方法,与适当的运动计划相结合,包括加强股内侧肌,以减轻PFPS患者的疼痛并增加功能。
    Patellofemoral pain syndrome (PFPS) is a set of symptoms that negatively affect the daily life activities of the individual, leading to functional disability and significant loss of labor, especially in young adults. PFPS is usually due to weakness of the vastus medialis obliquus (VMO) resulting in abnormal patellar tracking and pain. Our study aims to compare the efficacy of high-intensity laser therapy (HILT) on pain and lower extremity function in the treatment of PFPS with different electrophysical agents (EPAs). The study was designed as a single-blind randomized controlled trial. Forty-five people with PFPS (aged 25-45 years) were included in the study. The patients were randomly divided into three groups and a total of ten sessions of treatment were administered to all three groups for 2 weeks, 5 days a week. High-intensity laser (HILT) and exercise program were applied to group 1. Ultrasound (US), transcutaneous electrical nerve stimulation (TENS), and exercise program were applied to group 2. In group 3, US, interferential current (IFC), and exercise program were applied. Both groups underwent three evaluations: pre-treatment, post-treatment, and 12 weeks after treatment. Outcome measures included the visual analog scale for pain severity (VAS), knee flexion range of motion (FROM), Q angle, pain threshold, muscle strength of quadriceps and hamstring, Kujala patellofemoral scoring, lower extremity functional scale (LEFS), and Timed Up and Go Test (TUG). The ANOVA was used for comparing the data of the groups, and two-way repeated measure ANOVA was used to compare at the pre-post and post-intervention 3rd month. The LSD and Bonferroni post hoc tests were also used to identify the between-group differences. Groups 2 and 3 were statistically effective in pain and functionality (p < 0.05). Group 1 was found to be statistically more effective than other groups in reducing pain (95% confidence interval (CI), 0.000/0.000; p = 0.000), increasing knee flexion angle (95% CI, 127.524/135.809; p = 0.000), and increasing lower extremity function (95% CI, 75.970/79.362; p = 0.000). This study indicated that high-intensity laser therapy was found to be a more effective method in the treatment of patellofemoral pain syndrome after 3 months of follow-up compared to US-TENS combination and US-interferential current combination treatments. Also, HILT can be used as an effective method in combination with an appropriate exercise program including vastus medialis strengthening to reduce pain and increase functionality in the patients with PFPS.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Observational Study
    背景:与药物相关的问题是急诊科(ED)就诊的重要原因,多达60%的ED患者报告用药错误。诸如药物核对和药物审查之类的程序可以识别和防止与药物相关的问题和药物错误。然而,这项工作通常很耗时。在没有药剂师的ED中,药物和解是医生的责任,除了检查和诊断患者的主要任务。这项研究的目的是确定当ED中没有药剂师时,ED医生在药物相关任务上花费了多少时间。
    方法:使用工作观察法(WOMBAT)对挪威北部三个ED的医生进行了时间和运动观察研究,以收集和时间戳数据。在预定义的两小时观察会议中进行观察,观察者和参与者之间的关系为1:1。周一至周五上午8点至晚上8点,从2020年11月到2021年10月。
    结果:总计,在225次观察期间收集了386小时的观察结果。医生总共有8.7%的工作时间花在药物相关的任务上,其中大部分时间用于与其他医生(3.0%)和药物相关文件(3.2%)的口服沟通。医生每小时花费2.2分钟进行药物和解任务,其中包括直接从患者那里检索药物相关信息,阅读/检索书面药物相关信息,和药物相关的文件。医生在非药物相关的临床或管理任务上花费了85.6%的观察时间。剩下的时间是在任务之间待机或移动。
    结论:在三个挪威ED中,医生将8.7%的工作时间花在药物相关的任务上,其他临床或行政任务占85.6%。医生每小时花费2.2分钟完成与药物和解相关的任务。我们担心ED中与患者安全相关的任务很少受到关注。分配药剂师等专用资源来完成与药物相关的任务可以使医生和患者受益。
    BACKGROUND: Medication-related problems are an important cause of emergency department (ED) visits, and medication errors are reported in up to 60% of ED patients. Procedures such as medication reconciliation and medication review can identify and prevent medication-related problems and medication errors. However, this work is often time-consuming. In EDs without pharmacists, medication reconciliation is the physician\'s responsibility, in addition to the primary assignments of examining and diagnosing the patient. The aim of this study was to identify how much time ED physicians spend on medication-related tasks when no pharmacists are present in the EDs.
    METHODS: An observational time-and-motion study of physicians in three EDs in Northern Norway was conducted using Work Observation Method by Activity Timing (WOMBAT) to collect and time-stamp data. Observations were conducted in predefined two-hour observation sessions with a 1:1 relationship between observer and participant, during Monday to Friday between 8 am and 8 pm, from November 2020 to October 2021.
    RESULTS: In total, 386 h of observations were collected during 225 observation sessions. A total of 8.7% of the physicians\' work time was spent on medication-related tasks, of which most time was spent on oral communication about medications with other physicians (3.0%) and medication-related documentation (3.2%). Physicians spent 2.2 min per hour on medication reconciliation tasks, which includes retrieving medication-related information directly from the patient, reading/retrieving written medication-related information, and medication-related documentation. Physicians spent 85.6% of the observed time on non-medication-related clinical or administrative tasks, and the remaining time was spent standby or moving between tasks.
    CONCLUSIONS: In three Norwegian EDs, physicians spent 8.7% of their work time on medication-related tasks, and 85.6% on other clinical or administrative tasks. Physicians spent 2.2 min per hour on tasks related to medication reconciliation. We worry that patient safety related tasks in the EDs receive little attention. Allocating dedicated resources like pharmacists to contribute with medication-related tasks could benefit both physicians and patients.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    外周动脉和主动脉疾病会在各个领域造成复杂的后果,以及由于功能能力的逐渐限制或丧失而导致的身体和精神不适,特别是在步行方面,在体育锻炼期间耐力下降,努力容忍度下降,以及患者遭受的痛苦。功能能力的限制也增加了跌倒的风险。大多数跌倒发生在简单活动的执行过程中。这项研究的目的是调查与计划进行血管手术的患者未来跌倒的中至高风险相关的因素。
    这项横断面研究包括33-87岁的患者,计划进行血管手术。根据定时启动和启动测试,患者被分类为中至高(≥10s)或低跌倒风险.进行了多元逻辑回归以评估跌倒风险水平与独立的社会人口统计学和临床变量之间的关系。
    48%的患者被归类为未来跌倒的中度至高度风险。女性(OR=1.67;Cl95%:1.07-2.60)和患有高血压的患者(OR=2.54;Cl95%:1.19-5.40)与未来跌倒的中至高风险相关。Barthel指数呈负相关(OR=0.69;Cl95%:0.59-0.80),而年龄与跌倒风险水平呈正相关(OR=1.07;Cl95%:1.02-1.12)。
    可能与预定进行血管手术的患者未来跌倒的中至高风险相关的因素包括年龄,女性性别,高血压,和Barthel指数。
    Peripheral artery and aorta diseases contribute to complex consequences in various areas, as well as increasing physical and mental discomfort resulting from the progressive limitation or loss of functional capacities, in particular in relation to walking, decreased endurance during physical exercise, a drop in effort tolerance, and pain suffered by patients. Limitations in functional capacities also increase the risk of falls. Most falls take place during the performance of simple activities. The aim of this study was to investigate factors associated with moderate-to-high risk of future falls in patients scheduled for vascular surgeries.
    This cross-sectional study included patients aged 33-87, scheduled for vascular surgeries. Based on the Timed Up and Go test, patients were categorized as having a moderate-to-high (≥ 10 s) or low risk of falls. Multiple logistic regression was carried out to assess the relationship between fall-risk levels and independent sociodemographic and clinical variables.
    Forty-eight percent of patients were categorized as having a moderate-to-high risk of future falls. Females (OR = 1.67; Cl95%: 1.07-2.60) and patients who suffered from hypertension (OR = 2.54; Cl95%: 1.19-5.40) were associated with a moderate-to-high risk of future falls. The Barthel Index correlated negatively (OR = 0.69; Cl95%: 0.59-0.80), while age correlated positively with fall-risk levels (OR = 1.07; Cl95%: 1.02-1.12).
    Factors that may be associated with a moderate-to-high risk of future falls in patients scheduled for vascular surgeries include age, female gender, hypertension, and the Barthel Index.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    目的:本研究旨在确定以小组为基础的低至中度体育锻炼试点计划的可行性,教育和社会活动,通过调查可接受性,实用性,实施和功效测试。我们为未来的研究提供有关程序适应的建议。
    方法:邀请患有一系列慢性呼吸系统疾病的人参加为期12周的试点小组活动计划。活动包括户外散步,太极,教育和一系列社会活动。可接受性取决于在访谈期间确定的参与者经验。实用性取决于计划和成果衡量标准的完成情况,成本和不良事件。执行情况是根据方案是否按计划进行确定的。通过对结果的统计分析确定疗效,包括手握力,计时并进行测试,COPD无助指数,COPD评估测试,以及通过加速度测量法测量身体活动。
    结果:主题分析表明,“呼吸快乐”计划是可以接受的。9名与会者中有7人完成了10次会议中的8次,大多数人完成了所有成果衡量标准。因此,“呼吸快乐”被认为是实用的。方案没有按计划实施,只运行10个会话,而不是预期的12个。每日步数显着增加(MD:128495%CI:240-2329p:0.024效应大小:0.988),步进时间(MD:16分钟95%CI:5-27分钟p:0.011效应大小:1.36)和每天完成轻度体力活动的分钟(MD:2395%CI:6-38p:0.006效应大小:1.6)。然而,久坐≥30分钟但≤60分钟的时间显着增加(MD:2695%CI:0.2-52分钟p:0.049效应大小:0.931),显示出功效和改变身体活动行为模式的迹象。
    结论:一项为期10周的低中度体育锻炼计划,教育和社会活动显示出未来研究的可行性迹象。对未来研究的建议调整包括使用身体活动措施,如每日步数或轻度身体活动作为主要结果,以及与参与者对该计划的有益经验相关的心理健康和社会健康相关结果测量。在未来的研究中,招募人员将尝试接触那些社交活动较少的人以及可能已经完成肺康复(PR)的人。场地应靠近有效的交通联系,同时应试行不同的方案交付频率和持续时间。应为运行该计划的工作人员和盲目的研究人员提供足够的资金,以进行成果衡量。
    OBJECTIVE: This study aimed to determine the feasibility of a group-based pilot programme of low-to-moderate physical activity training, education and social activities, by investigating acceptability, practicality, implementation and efficacy testing. We offer suggestions on programme adaptions for future study.
    METHODS: People with a range of chronic respiratory diseases were invited to participate in a pilot 12 week group activity programme. Activities included outdoor walking, tai-chi, education and a range of social activities. Acceptability was determined by participant experiences determined during interviews. Practicality was determined by programme and outcome measure completion, cost and adverse events. Implementation was determined according to whether the programme ran as planned. Efficacy was determined by statistical analyses of outcomes including hand grip strength, timed up and go test, COPD Helplessness Index, COPD Assessment Test, and measures of physical activity via accelerometry.
    RESULTS: Thematic analysis indicated that the \"BreatheHappy\" programme was acceptable. Seven of nine participants completed eight out of 10 sessions and the majority completed all outcome measures. \"BreatheHappy\" was therefore considered practical. The programme was not implemented as planned, with only 10 sessions running rather than the 12 intended. There was a significant increase in daily step counts (MD: 1284 95% CI: 240-2329 p: 0.024 effect size: 0.988), stepping time (MD: 16 min 95% CI: 5-27 min p: 0.011 effect size: 1.36) and daily minutes completing light physical activity (MD: 23 95% CI: 6-38 p: 0.006 effect size: 1.6). However, time spent sitting for ≥30 min but ≤60 min significantly increased (MD: 26 95% CI: 0.2-52 min p: 0.049 effect size: 0.931), showing signs of efficacy and changing physical activity behaviour patterns.
    CONCLUSIONS: A 10-week programme of low-moderate physical activity training, education and social activities shows signs of feasibility for future research. Suggested adaptions for future study include using physical activity measures such as daily step count or light physical activity for a primary outcome, and mental health and social health related outcome measures relatable to participant\'s beneficial experiences of the programme. Recruitment in future studies will try and reach both those less socially active and possibly those who have completed pulmonary rehabilitation (PR). Venues should be close to efficient transport links whilst different frequencies and durations of programme delivery should be trialled. Adequate funding should be provided for both staff running the programme and blinded research staff for outcome measurement.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Journal Article
    背景:LeeSilverman语音治疗(LSVT)BIG是为帕金森氏症(PwPD)患者开发的一项运动计划,包括每周连续4天进行的练习集,共4周。然而,标准方案表明,对于大多数难以到达康复诊所的患者,治疗频率难以追踪.我们的目的是比较标准的LSVTBIG协议与改良的LSVT(m-LSVT)BIG协议(每周两次在诊所,为期4周,每周两次在家,为期4周)。
    方法:在这项随机对照试验中,16PwPD(年龄18-80岁,Hoehn和Yahr阶段I-III)被招募为两组。LSVT组接受标准LSVTBIG训练(每周四次,在诊所共4周)。另一组给予m-LSVTBIG练习,但与LSVT组不同,m-LSVT组每周在诊所锻炼两次,每周在家锻炼两次,共4周.Berg平衡量表用于评估功能平衡。Biodex平衡系统用于评估实验室平衡测量。定时Up和Go测试和G-Walk传感器系统用于评估功能移动性和时空步态分析。
    结果:发现改良的平衡感觉统合(F=10.138,p=.007)和步态周期对称指数(F=10.470,p=.010)的眼睛睁开-坚固表面评分的各组间的显著交互作用有利于LSVT组。此外,事后分析显示,两组都显著提高了姿势稳定性,步态速度,运动症状,和功能流动性(p<0.05)。
    结论:结果揭示了改良方案对PwPD平衡和步态的有益作用,以及标准LSVTBIG协议的优越性。m-LSVTBIG协议可能是一种有效的干预方法,特别是对于难以适应标准方案的治疗频率的PwPD。
    BACKGROUND: Lee Silverman voice treatment (LSVT) BIG is an exercise program developed for patients with Parkinson\'s disease (PwPD), consisting of sets of exercises performed for 4 consecutive days a week for 4 weeks. However, the standard protocol suggests a treatment frequency difficult to follow for most patients who have difficulties reaching rehabilitation clinics. Our aim was to compare the standard LSVT BIG protocol with a modified LSVT (m-LSVT) BIG protocol (twice a week in the clinic for 4 weeks and twice a week at home for 4 weeks).
    METHODS: In this randomized controlled trial, 16 PwPD (aged 18-80 years, Hoehn and Yahr stages I-III) were recruited into two groups. The LSVT group received standard LSVT BIG training (four times per week for 4 weeks at the clinic). The other group was given m-LSVT BIG exercises, but unlike the LSVT group, the m-LSVT group exercised twice a week at the clinic and twice a week at home for 4 weeks. The Berg Balance Scale was used to assess functional balance. Biodex Balance System was used to assess laboratory balance measures. Timed Up and Go test and G-Walk sensor system were used to assess functional mobility and spatiotemporal gait analysis.
    RESULTS: Significant group-by-time interactions on the eyes open-firm surface score of the modified clinical test of sensory integration of balance (F = 10.138, p = .007) and gait cycle symmetry index (F = 10.470, p = .010) were found to be in favor of the LSVT group. Additionally, post hoc analyses revealed that both groups significantly improved postural stability, gait speed, motor symptoms, and functional mobility (p < .05).
    CONCLUSIONS: The results revealed the beneficial effects of the modified protocol on balance and gait in PwPD, as well as the superiority of the standard LSVT BIG protocol. The m-LSVT BIG protocol may be an effective intervention method, especially for PwPD who have difficulty adapting to the treatment frequency of the standard protocol.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: English Abstract
    BACKGROUND: Professionals, especially in the field of digital public health (DiPH), are crucial for a successful digital transformation in social and health care. However, it is still unclear to what extent academic professionals are taught DiPH-related content in their public health (PH) studies.
    METHODS: This study used a systematic module handbook analysis to analyze accredited full-time PH-oriented degree programs at public colleges and universities in Germany for DiPH-related module content. Through the \"Hochschulkompass\" platform and the member programs of the German Public Health Association (DGPH), 422 programs were identified. Included module handbooks were evaluated by content analysis using MAXQDA.
    RESULTS: Only 10 bachelor and 6 master programs contain DiPH. They are heterogeneous in their focus and belong to different subfields of public health (\"methods, definition, history, and social medicine\" = 5; \"health management\" = 5; \"digital health\" = 3; \"health services research\" = 2; \"health communication\" = 1). Differences were found between the common understanding of DiPH in academia and the content in the module handbooks. The content identified in the analysis focuses mainly on technical areas. Social and health science content is only marginally present.
    CONCLUSIONS: The heterogeneous study programs with a connection to DiPH allow academic PH specialists to develop specific profiles. To achieve comprehensive competencies in DiPH, there is a need for further development of modules with relevance to the respective degree program. The results could be used for the (further) development of relevant modules and a core curriculum in DiPH.
    UNASSIGNED: HINTERGRUND: Fachkräfte für den Bereich Digital Public Health (DiPH) sind für eine erfolgreiche digitale Transformation im Sozial- und Gesundheitswesen notwendig. Unklar ist jedoch, inwiefern im Public-Health-(PH-)Studium DiPH-bezogene Inhalte vermittelt werden.
    METHODS: Mittels systematischer Modulhandbuchanalyse wurden DiPH-bezogene Inhalte von akkreditierten PH-orientierten Studiengängen öffentlicher Hochschulen und Universitäten in Deutschland analysiert. Über die Plattform „Hochschulkompass“ und Mitgliedsstudiengänge der Deutschen Gesellschaft für Public Health (DGPH) wurden 422 Studiengänge identifiziert. Eingeschlossene Modulhandbücher wurden inhaltsanalytisch mittels MAXQDA ausgewertet.
    UNASSIGNED: Lediglich 10 Bachelor- und 6 Masterstudiengänge weisen einen inhaltlichen DiPH-Bezug auf. Sie sind in ihren Schwerpunkten heterogen und unterschiedlichen PH-Teilbereichen zuzuordnen („Methoden, Definition, Geschichte und Sozialmedizin“ = 5; „Gesundheitsmanagement“ = 5; „Digital Health“ = 3; „Versorgungsforschung“ = 2; „Gesundheitskommunikation“ = 1). Zwischen dem wissenschaftlich gängigen Verständnis von DiPH und den darauf bezogenen Inhalten in den Modulhandbüchern zeigen sich Unterschiede. Die identifizierten Inhalte fokussieren eher technische und geringfügiger sozial- und gesundheitswissenschaftliche Bereiche.
    CONCLUSIONS: Die heterogenen Studiengänge mit DiPH-Bezug ermöglichen akademischen PH-Fachkräften eine spezifische Profilierung. Um umfassende Kompetenzen im Bereich DiPH zu erlangen, bedarf es eines weiteren Ausbaus entsprechender Module, die für den jeweiligen Studiengang relevant sind. Die Ergebnisse könnten zur (Weiter‑)Entwicklung geeigneter Module sowie eines DiPH-Kerncurriculums dienen.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

公众号