digital

数字
  • 文章类型: Journal Article
    背景:由于自身免疫性疾病和风湿性疾病(AIRD)患者的潜在病情,大流行给他们带来了独特的挑战,免疫抑制治疗的效果,增加疫苗的犹豫。
    目的:自身免疫性疾病(COVAD)中的COVID-19疫苗接种研究,一系列正在进行的,患者自我报告调查的设想是作为收集患者对AIRD观点的独特工具.它涉及一家跨国公司,在全球封锁中的多中心协作努力。
    方法:利用社交媒体作为研究工具,COVAD使用经过验证的患者报告结果(PRO)收集数据。这项研究,由一个核心团队组成,指导委员会,和全球合作者,促进数据收集和分析。经过飞行员测试,经过验证的调查,关于COVID-19感染的问题,疫苗接种和结果,患者人口统计学,并将PROs分发给患有AIRDs和健康对照(HCs)的患者。
    结论:我们提出了在这个国际合作项目中遇到的挑战,包括协调,数据管理,资金紧张,语言障碍,和作者的担忧,同时强调为解决这些问题而采取的措施。
    结论:协作虚拟模型为医学研究提供了一个动态的新前沿,对研究罕见疾病至关重要。COVAD研究证明了在线平台进行大规模、以患者为中心的研究,强调了将患者观点纳入临床护理的重要性。照顾病人是我们的核心动机,在研究影响他们的条件时,必须承认他们的声音是平等的利益相关者和有价值的伙伴。
    The pandemic presented unique challenges for individuals with autoimmune and rheumatic diseases (AIRDs) due to their underlying condition, the effects of immunosuppressive treatments, and increased vaccine hesitancy.
    The COVID-19 vaccination in autoimmune diseases (COVAD) study, a series of ongoing, patient self-reported surveys were conceived with the vision of being a unique tool to gather patient perspectives on AIRDs. It involved a multinational, multicenter collaborative effort amidst a global lockdown.
    Leveraging social media as a research tool, COVAD collected data using validated patient-reported outcomes (PROs). The study, comprising a core team, steering committee, and global collaborators, facilitated data collection and analysis. A pilot-tested, validated survey, featuring questions regarding COVID-19 infection, vaccination and outcomes, patient demographics, and PROs was circulated to patients with AIRDs and healthy controls (HCs).
    We present the challenges encountered during this international collaborative project, including coordination, data management, funding constraints, language barriers, and authorship concerns, while highlighting the measures taken to address them.
    Collaborative virtual models offer a dynamic new frontier in medical research and are vital to studying rare diseases. The COVAD study demonstrates the potential of online platforms for conducting large-scale, patient-focused research and underscores the importance of integrating patient perspective into clinical care. Care of patients is our central motivation, and it is essential to recognize their voices as equal stakeholders and valued partners in the study of the conditions that affect them.
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  • 文章类型: Journal Article
    本研究旨在验证数字化改良腮腺肿瘤分区方法在改良腮腺切口中的作用。收集2021年11月至2023年12月腮腺良性肿瘤患者的数据。通过运用数字化技术进行软组织重建,根据数字图像标记点将腮腺肿瘤分为四个区域。我们根据腮腺分区设计手术切口,发现通过分区指导切口选择是可行的,并总结了常见的切口和相应的划分,I区是I和V形切口,II区为V形切口,III区为V形和C形切口,IV区为C形切口。我们得出结论,数字改良腮腺分区方法可以在手术切口中提供更好的区分,并提供更好的美容切口和预后。
    The objective of this study is to verify the role of digital modified parotid tumor zoning method in modified parotid incision. The data of patients with parotid benign tumors from November 2021 to December 2023 were collected. Through the use of digital technology for soft tissue reconstruction, the parotid tumor was divided into four areas according to the digital image marker points. We designed the surgical incision according to the parotid gland division, found that it was feasible to guide the incision selection by division, and summarized the common incision and division corresponding, zone I was I and V-shaped incision, zone II was V incision, zone III was V and C- shaped incision, and zone IV was C- shaped incision. We conclude that the digital modified parotid gland zoning method can provide a better distinction in the surgical incision, and provide a better cosmetic incision and prognosis.
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  • 文章类型: Meta-Analysis
    目的:妇科癌症患者经常由于多种压力因素而出现心理问题。心理障碍对妇科癌症患者有衰弱的影响。近几十年来,数字社会心理干预措施已经迅速发展,并被纳入心理健康干预措施。数字社会心理干预可以为患者提供比传统的面对面干预更多的好处。包括便利性,匿名,灵活的调度,地理流动性。本系统综述的目的是综合数字心理社会干预在减少心理困扰方面的有效性,抑郁症,和焦虑和改善妇科癌症患者的健康相关生活质量。
    方法:2022年12月22日从9个书目数据库中进行了三步广泛搜索,审判登记处和灰色文献。包括涉及妇科癌症患者的实验研究,该研究利用数字心理社会干预措施来改善心理健康结果。采用RevMan5.4软件进行Meta分析。异质性通过Cochran的Q检验和I2进行分析。尝试进行亚组分析以评估亚组特征的相对效应大小。
    结果:9项研究的荟萃分析显示,与对照组相比,干预后抑郁减轻的效果较小(d=0.24,95%CI-0.46至-0.02),干预后心理困扰减轻的效果中等(d=0.51,95%CI-0.81至-0.21)和随访(d=0.65,95%CI-1.25至-0.05)。数字心理社会干预对焦虑和健康相关生活质量的影响无统计学意义。
    结论:与对照组相比,数字社会心理干预可能减轻了妇科癌症患者的心理困扰,并略微减轻了抑郁。可以融入临床实践。需要采用严格方法和更大样本量的其他试验来验证结果。
    背景:PROSPERO(CRD42023389502)。
    OBJECTIVE: Patients with gynaecological cancer often experience psychological issues due to multiple stressors. Psychological disturbances have debilitating effects on patients with gynaecological cancer. In recent decades, digital psychosocial interventions have rapidly advanced and been incorporated into mental health interventions. Digital psychosocial interventions could provide patients with several benefits over traditional in-person interventions, including convenience, anonymity, flexible scheduling, and geographic mobility. The aim of this systematic review was to synthesize the effectiveness of digital psychosocial intervention in reducing psychological distress, depression, and anxiety and improving health-related quality of life in patients with gynaecological cancer.
    METHODS: Three-step extensive search was performed on 22 December 2022 from nine bibliographic databases, trial registries and grey literature. Experimental studies involving patients with gynaecological cancer utilizing digital psychosocial interventions for the improvement of mental health outcomes were included. Meta-analysis was conducted using RevMan 5.4 software. Heterogeneity was analysed by Cochran\'s Q test and I2. Subgroup analyses were attempted to evaluate relative effect sizes of subgroup features.
    RESULTS: Meta-analysis of nine studies revealed small effect size in reduction of depression post-intervention (d = 0.24, 95% CI - 0.46 to - 0.02) and medium effect size in reduction of psychological distress post-intervention (d = 0.51, 95% CI - 0.81 to - 0.21) and follow-up (d = 0.65, 95% CI - 1.25 to - 0.05) compared to the control group. The effects of digital psychosocial interventions on anxiety and health-related quality of life were not statistically significant.
    CONCLUSIONS: Digital psychosocial interventions probably reduced psychological distress and slightly reduced depression amongst patients with gynaecological cancer compared to the control group, which can be integrated into clinical practice. Additional trials with rigorous methodology and bigger sample sizes are needed to validate findings.
    BACKGROUND: PROSPERO (CRD42023389502).
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  • 文章类型: Journal Article
    心血管疾病已成为影响我国人民健康的主要疾病负担。血管对人体健康非常重要,是许多心脑血管疾病发展的“前哨”。有效预防致命的关键,致残心脏,脑和外周血管事件在于从源头上控制血管健康的传统和非传统危险因素,早期血管病变的早期评估和干预。2004年以来,我国政府推广血管病变早期检测技术和血管医学,并提出了北京血管健康分层(BVHS)的检查建议,风险因素的评估和管理,为血管健康的终身维护提供新思路。本文主要介绍我国近20年来"血管医学"临床学科的建立和发展,介绍了血管功能和结构的检测指标以及血管事件的预测价值,并在个性化预防的整个生命周期中对血管健康进行智能化和数字化管理,对不同部位或程度病变的人进行治疗和康复,有效减少心脑血管疾病的发生和发展,以及维持血管健康的新技术的前景。
    Cardiovascular disease(CVD) has become a major disease burden affecting people\'s health in China. Blood vessels are very important for human health and are the \"sentinel\" for the development of many cardiovascular and cerebrovascular diseases. The key to effectively preventing fatal, disabling heart, brain and peripheral vascular events lies in controlling traditional and non-traditional risk factors for vascular health from the source, and early assessment and intervention of early vascular lesions. Since 2004, China government promoted the early detection technology of vascular lesions and vascular medicine, and proposed the Beijing Vascular Health Stratification (BVHS) to provide suggestions for the examination, evaluation and management of risk factors, and to provide new ideas for lifelong maintenance of vascular health. This review mainly introduces the establishment and development of the clinical discipline of \"vascular medicine\" in the past 20 years in China, introduces the indicators for detecting vascular function and structure and the predictive value of vascular events, and carries out intelligent and digital management of vascular health throughout the life cycle of individualized prevention, treatment and rehabilitation for people with different parts or degrees of lesions, effectively reducing the occurrence and development of cardiovascular and cerebrovascular diseases, and the prospect of new technology in maintaining vascular health.
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  • 文章类型: Journal Article
    慢性失眠的数字认知行为疗法(D-CBT-I)已被证明与传统的CBT-I一样有效。然而,并非所有患者在治疗后都能实现失眠缓解。我们探讨了影响D-CBT-I在临床实践中的有效性的因素。在为期6周的D-CBT-I干预期间,共研究了414例亚洲慢性失眠患者。所有患者在基线和治疗后进行评估,并被确定为缓解者或非缓解者,根据治疗后标准,有反应者或无反应者;失眠严重程度指数(ISI<8)或ISI降低≥8,以检查缓解和反应状态是否与患者基线特征相关。所有受试者的平均基线ISI评分为16.29分。在治疗后,192例(46.4%)患者实现了ISI缓解,218例(52.7%)患者表现出ISI反应。基线清晨觉醒时间和ISI评分的增加与较低的缓解几率独立相关(OR,分别为0.995和0.991)。基线患者健康问卷-9得分增加与较高的反应几率独立相关(OR,1.114).我们的结果表明,D-CBT-I可以推荐作为慢性失眠的一线治疗,特别是失眠患者,失眠症状较轻,抑郁症状更严重。同时,D-CBT-I的有效性受到较长的清晨觉醒时间和较高的失眠严重程度的不利影响,可以通过更强烈的干预和更大的治疗支持或传统的CBT-I来改善。
    Digital cognitive behavioural therapy for chronic insomnia (D-CBT-I) has been shown to be as efficacious as traditional CBT-I. However, not all patients achieve insomnia remission after treatment. We explored the factors influencing the effectiveness of D-CBT-I in a clinical practice. A total of 414 Asian chronic insomniacs were studied during a 6 week D-CBT-I intervention. All patients were assessed at baseline and posttreatment and were determined to be remitters or non-remitters, responders or non-responders by posttreatment criteria; Insomnia Severity Index (ISI <8) or ISI reduction ≥8, to examine whether remission and response status were associated with patient baseline characteristics. The average baseline ISI score in all subjects was 16.29 points. At posttreatment, 192 (46.4%) patients achieved ISI remission and 218 (52.7%) patients demonstrated an ISI response. An increased baseline early morning awakening time and ISI score were independently associated with a lower odds for remission (OR, 0.995 and 0.991, respectively). Increased baseline Patients Health Questionnaire-9 score was independently associated with higher odds for response (OR, 1.114). Our results suggest that D-CBT-I can be recommended as the first-line treatment for chronic insomnia, particularly in insomniacs with milder insomnia symptoms and more severe depressive symptoms. Meanwhile, the effectiveness of D-CBT-I was adversely affected by longer early morning awakening time and higher insomnia severity at pretreatment, which may be improved by more intense intervention and greater therapeutic support or by traditional CBT-I.
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  • 文章类型: Journal Article
    数字重组酶聚合酶扩增(dRPA)旨在通过将核酸和RPA反应所需的所有试剂均匀地分成许多单独的反应单元来量化核酸的初始量。如腔室或液滴。由于dRPA具有设备要求低的优点,因此被证明是定量靶核酸绝对量的重要技术,短时间消费,以及高灵敏度和特异性。dRPA结合微流体被认为是简单的,各种,和高通量核酸量化系统。本文对过去十年的微流控dRPA系统进行了分类。我们分析和总结了各种微流体dRPA系统的重要技术(例如,芯片制备过程,分割原则,微流控,和统计分析方法),以及解决局限性的主要努力(例如,防止蒸发和污染,精确的启动,并减少手动操作)。此外,本文总结了微流控dRPA成功的关键因素和潜在制约因素,以帮助更多的研究人员,以及克服上述挑战的可能策略。最后,提出了微流控dRPA后续发展的实际建议和策略。
    Digital recombinase polymerase amplification (dRPA) aims to quantify the initial amount of nucleic acid by dividing nucleic acid and all reagents required for the RPA reaction evenly into numerous individual reaction units, such as chambers or droplets. dRPA turns out to be a prominent technique for quantifying the absolute quantity of target nucleic acid because of its advantages including low equipment requirements, short time consumption, as well as high sensitivity and specificity. dRPA combined with microfluidics are recognized as simple, various, and high-throughput nucleic acid quantization systems. This paper classifies the microfluidic dRPA systems over the last decade. We analyze and summarize the vital technologies of various microfluidic dRPA systems (e.g., chip preparation process, segmentation principle, microfluidic control, and statistical analysis methods), and major efforts to address limitations (e.g., prevention of evaporation and contamination, accurate initiation, and reduction of manual operation). In addition, this paper summarizes key factors and potential constraints to the success of the microfluidic dRPA to help more researchers, and possible strategies to overcome the mentioned challenges. Lastly, actual suggestions and strategies are proposed for the subsequent development of microfluidic dRPA.
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  • 文章类型: Journal Article
    目的:本研究旨在介绍一种使用骨水泥和K线组合的外固定技术,治疗与手指关节附近的孤立性数字内生软骨瘤有关的病理性骨折。
    方法:自2015年10月至2021年1月,对21例(男8例,女13例)手指关节附近孤立性指内软骨瘤引起的急性病理性骨折患者采用骨水泥型K线外固定器治疗。平均年龄为32(19至51)岁。涉及的数字是指数(n=4),长(n=4),环(n=6),和小(n=7)的手指。评估骨愈合时间和并发症。在最后的后续行动中,活动范围,测量并比较受累肿瘤和对侧健康手指的握力和关键捏力。根据Takigawa标准评估功能结果。以10cm视觉模拟量表测量疼痛。我们在肌肉骨骼肿瘤学会评分问卷上评估了受影响的上肢。
    结果:平均骨愈合时间为5.5(4-8)周。在1例患者中观察到引脚部位感染,并通过换药治愈。平均随访34个月,没有复发或折射。近端指间关节的平均活动范围,所涉及的数字的抓地力和键捏强度达到92%,97%,99%的对侧手指,分别。在高川标准上,20个机能成果为优,1个为好。平均疼痛评分为1(0至3)cm。肌肉骨骼肿瘤协会平均评分为95(80-100)。
    结论:骨水泥和K线的组合是一种可靠的技术,用于治疗与手指关节附近的孤立性内生软骨瘤有关的病理性骨折,导致良好的功能结果。
    方法:治疗性研究,IVa级。
    This study aimed to introduce a technique of external fixation using a combination of bone cement and K-wires, to treat pathological fractures related to solitary digital enchondroma close to the finger joints.
    From October 2015 to January 2021, 21 patients (8 males and 13 females) with acute pathological fracture due to solitary digital enchondroma close to the finger joints were treated with cemented K-wire external fixators. Mean age was 32 (19-51) years. The digits involved were the index (n = 4), long (n = 4), ring (n = 6), and little (n = 7) fingers. Time to bone healing and complications were assessed. At final follow-up, active range of motion, grip strength and key pinch strength of the tumor-involved and contralateral healthy digits were measured and compared. Functional outcomes were evaluated on Takigawa criteria. Pain was measured on a 10-cm visual analog scale. We assessed the affected upper extremity on the Musculoskeletal Tumor Society score questionnaire.
    Mean bone healing time was 5.5 (4-8) weeks. Pin site infection was observed in 1 patient and cured with dressing changes. Mean follow-up was 34 months, with no recurrences or refractures. Mean active range of motion of the proximal interphalangeal joint, grip and key pinch strength of the involved digits reached 92%, 97%, and 99% of the contralateral digits, respectively. On Takigawa criteria, 20 functional results were excellent and 1 good. Mean pain score was 1 (0-3) cm. Mean Musculoskeletal Tumor Society score was 95 (80-100).
    The combination of bone cement and K-wires is a reliable technique for pathological fracture related to solitary enchondroma close to the joints of the digits, leading to good functional outcomes.
    Therapeutic study, Level IVa.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Journal Article
    背景:在产科护理模式中整合远程医疗对于为可能的感染暴发做好准备非常重要,这些感染暴发需要社交距离并限制面对面咨询。为确保产科远程健康在香港成功实施,了解和解决孕妇的担忧至关重要。
    目的:本研究旨在评估孕妇的态度,关注,以及对香港远程医疗产科诊所服务的看法。
    方法:我们于2021年11月至2022年8月在玛丽医院进行了一项前瞻性横断面问卷调查研究。利用5分评分量表,问卷旨在捕捉孕妇的偏好,期望,可行性感知,以及与远程医疗诊所服务有关的隐私问题。我们使用了统计分析,包括卡方检验和多项逻辑回归,比较问卷的回答,并调查怀孕和对远程医疗诊所的态度之间的关系。
    结果:该研究包括分布在不同妊娠阶段的664名参与者:在18孕周之前的269名(40.5%),在24至31周之间有198(29.8%),和197(29.7%)交货后。其中,49.8%(329/664)赞成面对面咨询,而不是远程医疗诊所,只有7.3%(48/664)的人认为相反。此外,24.2%(161/664)同意应开设远程保健诊所进行产科服务。然而,对远程医疗诊所的总体偏好是<20%的常规产前检查(81/664,12.2%)和解决与怀孕相关的问题,如阴道出血(76/664,11.5%),阴道分泌物(128/664,19.4%),胎动减少(64/664,9.7%),子宫收缩(62/664,9.4%),和怀疑羊水渗漏(54/664,8.2%)。相反,76.4%(507/664)更喜欢远程医疗诊所,而不是当面访问产前教育讲座,产前和产后锻炼,解决母乳喂养问题。参与者对远程医疗诊所的任务更满意,例如解释怀孕检查结果(418/664,63.1%),在家自行使用小便试纸(373/664,56.4%),病史记录(341/664,51.5%),和使用电子机器自我监测血压(282/664,42.8%)。%).在产后期间,与妊娠18周前相比,更多的参与者同意远程医疗诊所可以作为评估阴道出血等身体症状的一种选择(aOR2.105,95%CI1.448-3.059),胎动减少(aOR1.575,95%CI1.058-2.345),子宫收缩(aOR2.906,95%CI1.945-4.342),疑似羊水渗漏(aOR2.609,95%CI1.721-3.954),发烧(aOR1.526,95%CI1.109-2.100),和流感样症状(aOR1.412,95%CI1.030-1.936)。他们对测量联合基底高度也更有信心,安排进一步调查,并通过远程医疗诊所与医生进行诊断。远程医疗诊所的主要感知公共卫生优势是较短的旅行和等待时间(526/664,79.2%),而主要关注的是错误诊断和治疗的法律问题(511/664,77.4%)。
    结论:面对面咨询仍然是参与者的首选咨询方式。然而,远程健康诊所可以替代不需要体检或联系的服务。随着妊娠的进行和分娩后,人们对远程医疗的接受度和信心增加。执行更严格的法律和准则可以促进远程保健诊所的实施,并增加孕妇对使用远程保健诊所进行产科护理的信心。
    Integrating telehealth in an obstetric care model is important to prepare for possible infection outbreaks that require social distancing and limit in-person consultations. To ensure the successful implementation of obstetric telehealth in Hong Kong, it is essential to understand and address pregnant women\'s concerns.
    This study aimed to assess pregnant women\'s attitudes, concerns, and perceptions regarding telehealth obstetric clinic services in Hong Kong.
    We conducted a prospective cross-sectional questionnaire study at Queen Mary Hospital between November 2021 and August 2022. Utilizing a 5-point rating scale, the questionnaire aimed to capture pregnant women\'s preferences, expectations, feasibility perceptions, and privacy concerns related to telehealth clinic services. We used statistical analyses, including chi-square tests and multinomial logistic regression, to compare questionnaire responses and investigate the association between advancing gestation and attitudes toward telehealth clinics.
    The study included 664 participants distributed across different pregnancy stages: 269 (40.5%) before 18 gestational weeks, 198 (29.8%) between 24 and 31 weeks, and 197 (29.7%) after delivery. Among them, 49.8% (329/664) favored face-to-face consultations over telehealth clinics, and only 7.3% (48/664) believed the opposite. Additionally, 24.2% (161/664) agreed that telehealth clinics should be launched for obstetric services. However, the overall preference for telehealth clinics was <20% for routine prenatal checkups (81/664, 12.2%) and addressing pregnancy-related concerns, such as vaginal bleeding (76/664, 11.5%), vaginal discharge (128/664, 19.4%), reduced fetal movement (64/664, 9.7%), uterine contractions (62/664, 9.4%), and suspected leakage of amniotic fluid (54/664, 8.2%). Conversely, 76.4% (507/664) preferred telehealth clinics to in-person visits for prenatal education talks, prenatal and postpartum exercise, and addressing breastfeeding problems. Participants were more comfortable with telehealth clinic tasks for tasks like explaining pregnancy exam results (418/664, 63.1%), self-administering urinary dipsticks at home (373/664, 56.4%), medical history-taking (341/664, 51.5%), and self-monitoring blood pressure using an electronic machine (282/664, 42.8%). %). During the postpartum period, compared to before 18 weeks of gestation, significantly more participants agreed that telehealth clinics could be an option for assessing physical symptoms such as vaginal bleeding (aOR 2.105, 95% CI 1.448-3.059), reduced fetal movement (aOR 1.575, 95% CI 1.058-2.345), uterine contractions (aOR 2.906, 95% CI 1.945-4.342), suspected leakage of amniotic fluid (aOR 2.609, 95% CI 1.721-3.954), fever (aOR 1.526, 95% CI 1.109-2.100), and flu-like symptoms (aOR 1.412, 95% CI 1.030-1.936). They were also more confident with measuring the symphysis-fundal height, arranging further investigations, and making diagnoses with the doctor via the telehealth clinic. The main perceived public health advantage of telehealth clinics was the shorter traveling and waiting time (526/664, 79.2%), while the main concern was legal issues from wrong diagnosis and treatment (511/664, 77.4%).
    Face-to-face consultation remained the preferred mode of consultation among the participants. However, telehealth clinics could be an alternative for services that do not require physical examination or contact. An increased acceptance of and confidence in telehealth was found with advancing gestation and after delivery. Enforcing stricter laws and guidelines could facilitate the implementation of telehealth clinics and increase confidence in their use among pregnant women for obstetric care.
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  • 文章类型: Journal Article
    背景:精神病是最致残的精神健康状况之一,社会,和经济负担。准确和及时的症状监测对于提供及时和时间敏感的临床服务至关重要。数字健康是解决传统症状监测方法遇到的障碍的有前途的解决方案,包括可访问性,评估的生态有效性,和回忆偏见。然而,到目前为止,在中国,还没有开发出支持精神病患者自我管理的数字健康技术。
    目的:我们报告研究方案以评估其有效性,可行性,可接受性,可用性,以及针对中国精神病患者的症状自我监测智能手机应用程序(优信;中文名称)的安全性。
    方法:这是一项采用混合方法设计的非随机有效性和可行性研究。该研究获得了曼彻斯特大学和北京安定医院研究伦理委员会的批准。YouXin是一款智能手机应用程序,旨在促进精神病患者的症状自我监测。优信有2个核心功能:主动监测症状(即,智能手机调查)和行为活动的被动监控(即,通过嵌入式智能手机传感器进行被动数据收集)。友信的开发过程采用了系统的协同生产方法。主要研究人员与服务用户和临床医生举行了一系列联合生产咨询会议,以最大程度地提高应用程序对最终用户的可用性和可接受性。从北京安定医院招募16岁至65岁的精神病患者,北京,中国。所有参与者都被邀请使用YouXin应用程序自我监测症状4周。在为期4周的随访结束时,我们邀请参与者参加定性访谈,以探讨干预后应用程序和试验程序的可接受性。
    结果:该研究的招募于2022年8月开始。在2022年8月至2022年10月接受研究的47名参与者中,有41名参与者同意参加研究。我们排除了41名参与者中的1名不符合入选标准,共有40名参与者开始了这项研究。截至2022年12月,40名参与者完成了这项研究,招聘已经完成。
    结论:这项研究是首次开发和测试专门为中国精神病患者设计的症状自我监测应用程序。如果研究表明有新的可行性,一个潜在的未来方向是将该应用程序整合到临床工作流程中,以促进中国精神病患者的数字精神卫生保健。这项研究将为应用程序提供改进,审判程序,以及与该人群的实施策略。此外,这项试验的结果可能导致为中国精神病患者设计的数字健康技术的优化.
    DERR1-10.2196/45170。
    BACKGROUND: Psychosis is one of the most disabling mental health conditions and causes significant personal, social, and economic burden. Accurate and timely symptom monitoring is critical to offering prompt and time-sensitive clinical services. Digital health is a promising solution for the barriers encountered by conventional symptom monitoring approaches, including accessibility, the ecological validity of assessments, and recall bias. However, to date, there has been no digital health technology developed to support self-management for people with psychosis in China.
    OBJECTIVE: We report the study protocol to evaluate the validity, feasibility, acceptability, usability, and safety of a symptom self-monitoring smartphone app (YouXin; Chinese name ) for people with psychosis in China.
    METHODS: This is a nonrandomized validity and feasibility study with a mixed methods design. The study was approved by the University of Manchester and Beijing Anding Hospital Research Ethics Committee. YouXin is a smartphone app designed to facilitate symptom self-monitoring for people with psychosis. YouXin has 2 core functions: active monitoring of symptoms (ie, smartphone survey) and passive monitoring of behavioral activity (ie, passive data collection via embedded smartphone sensors). The development process of YouXin utilized a systematic coproduction approach. A series of coproduction consultation meetings was conducted by the principal researcher with service users and clinicians to maximize the usability and acceptability of the app for end users. Participants with psychosis aged 16 years to 65 years were recruited from Beijing Anding Hospital, Beijing, China. All participants were invited to use the YouXin app to self-monitor symptoms for 4 weeks. At the end of the 4-week follow-up, we invited participants to take part in a qualitative interview to explore the acceptability of the app and trial procedures postintervention.
    RESULTS: Recruitment to the study was initiated in August 2022. Of the 47 participants who were approached for the study from August 2022 to October 2022, 41 participants agreed to take part in the study. We excluded 1 of the 41 participants for not meeting the inclusion criteria, leaving a total of 40 participants who began the study. As of December 2022, 40 participants had completed the study, and the recruitment was complete.
    CONCLUSIONS: This study is the first to develop and test a symptom self-monitoring app specifically designed for people with psychosis in China. If the study shows the feasibility of YouXin, a potential future direction is to integrate the app into clinical workflows to facilitate digital mental health care for people with psychosis in China. This study will inform improvements to the app, trial procedures, and implementation strategies with this population. Moreover, the findings of this trial could lead to optimization of digital health technologies designed for people with psychosis in China.
    UNASSIGNED: DERR1-10.2196/45170.
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