Integrative Medicine

中西医结合
  • 文章类型: Editorial
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    艾灸作为一种传统的中医疗法有着悠久的历史。红外辐射是影响艾灸效果的重要因素。而不是用手拿艾条费时费力的过程,艾灸装置是现代常用的艾灸方法和工具。随着艾灸器械国际标准(ISO18666:2021,中医-艾灸器械的一般要求)的发布,现在在药店和网上商店出售各种材料的艾灸装置。然而,艾灸装置对艾灸治疗效果的影响尚未研究。因此,这项研究旨在评估艾灸装置的红外辐射,为了选择提供最接近艾条燃烧的红外辐射的艾灸装置。燃烧稳定性和红外辐射强度的组合表明,纸板管和硅胶是用于艾灸装置的较好材料。在中远红外波段,由纸板管和硅胶制成的艾灸装置可以更好地保持艾灸产生的热效应,使其更容易被人体吸收。纸板艾灸装置的红外辐射强度迅速而稳定地增加,并且可以保持最长的时间。总之,相对于红外辐射,纸板管是用于艾灸装置的较好材料。
    Moxibustion has a long history of use as a traditional Chinese medicine therapy. Infrared radiation is an important and effective factor in moxibustion. Instead of the time-consuming and laborious process of holding moxa sticks in the hand, moxibustion devices are commonly used as moxibustion methods and tools in modern times. With the publication of the international standard of moxibustion devices (ISO18666:2021, Traditional Chinese Medicine - General requirements of moxibustion devices) published, moxibustion devices of various materials are now sold in the pharmacies and online stores. However, the influence of moxibustion devices on the therapeutic effect of moxibustion has not been studied. Therefore, this research was aimed to evaluate the infrared radiation of moxibustion devices, in order to select the moxibustion device that delivered infrared radiation closest to that of moxa stick combustion. The combination of combustion stability and infrared radiation intensity showed that cardboard tubes and silicone were better materials for moxibustion devices. In the mid-far infrared wave band, the moxibustion devices made from cardboard tubes and silica gels can better maintain the thermal effect generated by moxibustion and enable it to be more easily absorbed by the human body. The infrared radiation intensity of the cardboard moxibustion devices increased rapidly and steadily and could be maintained for the longest time. In conclusion, cardboard tubes are the better material for moxibustion devices with respect to infrared radiation.
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  • 文章类型: Journal Article
    睡眠对于保持身心健康至关重要,包括皮肤健康。目前,人们对使用草药和天然成分来减轻睡眠障碍的不利影响越来越感兴趣。在这4周内,随机化,双盲,对照试验,70名患有睡眠障碍的受试者被随机分配接受安慰剂或Poriacocos,刺梨,和GABA(PZG)补充剂(每天10mL)。通过腕关节肌动仪检测总睡眠持续时间,通过匹兹堡睡眠质量指数(PSQI)评估睡眠质量。根据皮肤水合的评估来评估皮肤状况,光泽度弹性,颜色,皱纹的严重程度,和皮肤粗糙。4周后,与基线相比,总睡眠持续时间显著增加12.96%(p=.006),PSQI评分显著降低59.94%(p=.000).值得注意的是,与基线条件相比,皮肤水合作用,辐射,弹性,坚定,皱纹严重程度,PZG组粗糙度明显改善。此外,PZG组的总睡眠时间相对于基线的变化明显优于安慰剂组,PSQI得分,皮肤水合作用,皱纹严重程度,和皮肤粗糙。目前的结果表明,草药和GABA的联合摄入可以改善睡眠质量并增强皮肤健康,而不会产生不利影响。
    Sleep is crucial for preserving both physical and mental health, including skin health. Presently, there is a burgeoning interest in the use of herbal and natural ingredients to mitigate the adverse effects of sleep disorders. In this 4-week, randomized, double-blind, controlled trial, 70 subjects with sleep disorders were randomly assigned to receive either a placebo or a Poria cocos, Ziziphus spinose, and GABA (PZG) supplement (10 mL per day). Total sleep duration was detected by wrist actigraphy, and sleep quality was assessed by the Pittsburgh Sleep Quality Index (PSQI). Skin conditions were evaluated based on assessments of skin hydration, glossiness elasticity, color, severity of wrinkles, and skin roughness. After 4 weeks, the total sleep duration significantly increased by 12.96% (p = .006) and the PSQI score notably decreased by 59.94% (p = .000) compared to the baseline. Notably, compared to the baseline conditions, skin hydration, radiance, elasticity, firmness, wrinkle severity, and roughness were significantly improved in the PZG group. In addition, the PZG group demonstrated significantly greater improvements than the placebo group in terms of changes from baseline in total sleep duration, PSQI score, skin hydration, wrinkle severity, and skin roughness. The present results demonstrated that the combined intake of herbs and GABA can improve sleep quality and enhance skin health without adverse effects.
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  • 文章类型: Journal Article
    鉴于中成药(CPM)与5-氨基水杨酸(5-ASA)联合用于溃疡性结肠炎(UC)患者的广泛使用,本研究旨在评估9种CPM联合5-ASA治疗UC的有效性和安全性。
    从开始到2023年5月,在8个数据库中进行了系统的文献检索,以确定评估CPM联合5-ASA治疗UC效果的合格随机对照试验。使用ReviewManager5.4中的Cochrane偏倚风险工具评估纳入的RCT的方法学质量。荟萃分析的主要结果是总反应率。次要结果包括优良率,疾病活动指数(DAI),IL-6、IL-8和TNF-α水平,平均血小板体积(MPV),纤维蛋白原(FIB)水平,复发率,和不良事件发生率。使用ReviewManager5.4和Stata15.0进行网络荟萃分析。
    总共,纳入70个RCTs,包括5973例患者和10个治疗方案。康复新液(KFL)和5-ASA的组合在改善FIB水平和总有效率方面表现出最大的功效。补脾益肠丸(BYP)联合5-ASA治疗的不良反应最少,复发率最低。Hudi肠溶胶囊(HEC)联合5-ASA在改善DAI方面排名第一。致康胶囊(ZKC),肠炎宁胶囊(CYN),丹参注射液(DSI)联合5-ASA在改善IL-6、IL-10、TNF-α水平方面排名第一,分别。参苓白术散(SBP)联合5-ASA的优良率最高。
    CPM联合5-ASA治疗UC可能比单独的5-ASA更有效。此外,CPM联合5-ASA能更好地降低UC患者的复发率和不良事件发生率。目前的荟萃分析为临床应用提供了统计学证据。系统审查注册:国际前瞻性系统审查注册(PROSPERO),不。CRD42023433672。
    UNASSIGNED: Given the widespread use of Chinese patent medicines (CPMs) in combination with 5-aminosalicylic acid (5-ASA) for Ulcerative colitis (UC) patients, this study aimed to evaluate the efficacy and safety of nine CPMs combined with 5-ASA in the treatment of UC.
    UNASSIGNED: A systematic literature search was conducted in eight databases from inception to May 2023 to identify eligible RCTs evaluating the effects of CPM combined with 5-ASA for the treatment of UC. The methodological quality of the included RCTs was assessed using the Cochrane risk of bias tool in Review Manager 5.4. The primary outcome of the meta-analysis was the overall response rate. The secondary outcomes included excellent rate, disease activity index (DAI), IL-6, IL-8, and TNF-α levels, mean platelet volume (MPV), fibrinogen (FIB) levels, recurrence rate, and adverse event rate. Network meta-analysis was performed using Review Manager 5.4 and Stata 15.0.
    UNASSIGNED: In total, 70 RCTs including 5973 patients and 10 treatment regimens were included. The combination of Kangfuxin Liquid (KFL) and 5-ASA showed the greatest efficacy in improving FIB levels and the overall response rate. Bupi Yichang Pill (BYP) combined with 5-ASA was associated with the fewest adverse events and the lowest recurrence rate. Hudi Enteric-coated Capsule (HEC) combined with 5-ASA ranked first in improving DAI. ZhiKang Capsule (ZKC), ChangYanNing Capsule (CYN), and Danshen Injection (DSI) combined with 5-ASA ranked first in improving IL-6, IL-10, and TNF-α levels, respectively. Shenling Baizhu Powder (SBP) combined with 5-ASA was associated with the highest excellent rate.
    UNASSIGNED: CPM combined with 5-ASA may be more effective than 5-ASA alone for treating UC. Besides, CPM combined with 5-ASA could better reduce the recurrence rate and adverse event rate in UC patients. The current meta-analysis provides statistical evidence for clinical application.Systematic Review Registration: International Prospective Register of Systematic Reviews (PROSPERO), No. CRD42023433672.
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  • 文章类型: Journal Article
    背景:糖尿病会导致慢性肾脏疾病(CKD)和肾衰竭,需要透析或移植。黄芪,一种常见的草药和美国药典注册的食品成分,通过回顾性和临床前数据显示肾脏具有保护作用,但长期前瞻性临床证据有限。该试验旨在评估黄芪对糖尿病CKD患者肾功能下降的有效性。
    方法:这是随机的,评估员-盲,标准护理控制,2018年7月至2022年4月,多中心临床试验从7家公共门诊诊所和香港社区随机分配了118例估计肾小球滤过率(eGFR)为30~90ml/min/1.73m2,尿白蛋白与肌酐比值(UACR)为300~5000mg/g的患者,接受口服黄芪颗粒(每日15g生药当量)或单独继续标准治疗作为对照48周.主要结果是eGFR变化的斜率(用于样本量计算)和意向治疗人群的UACR。次要结果包括终点血压,生物化学,生物标志物,伴随的药物变化和不良事件。(ClinicalTrials.gov:NCT03535935)结果:在48周期间,使用黄芪时,eGFR下降斜率的估计差异为每年4.6ml/min/1.73m2(95CI:1.5~7.6,p=0.003).对于UACR,估计的组间变化斜率的比例差异不显著(1.14,95CI:0.85~1.52,p=0.392).记录了31例黄芪治疗患者和41例标准护理控制患者的117例不良事件。在黄芪治疗的患者中,48周的终点收缩压降低了7.9mmHg(95CI:-12.9至-2.8,p=0.003)。113例(96%)和107例(91%)患者有随机化后和终点主要结局指标,分别。
    结论:在2型糖尿病患者中,2至3期CKD和大量白蛋白尿,添加黄芪48周,在标准护理的基础上进一步稳定肾功能。
    BACKGROUND: Diabetes leads to chronic kidney disease (CKD) and kidney failure, requiring dialysis or transplantation. Astragalus, a common herbal medicine and US pharmacopeia-registered food ingredient, is shown kidney protective by retrospective and preclinical data but with limited long-term prospective clinical evidence. This trial aimed to assess the effectiveness of astragalus on kidney function decline in macroalbuminuric diabetic CKD patients.
    METHODS: This randomized, assessor-blind, standard care-controlled, multi-center clinical trial randomly assigned 118 patients with estimated glomerular filtration rate (eGFR) of 30-90 ml/min/1.73m2 and urinary albumin-to-creatinine ratio (UACR) of 300-5000 mg/g from 7 public outpatient clinics and the community in Hong Kong between July 2018 and April 2022 to add-on oral astragalus granules (15 gs of raw herbs daily equivalent) or to continue standard care alone as control for 48 weeks. Primary outcomes were the slope of change of eGFR (used for sample size calculation) and UACR of the intention-to-treat population. Secondary outcomes included endpoint blood pressures, biochemistry, biomarkers, concomitant drug change and adverse events. (ClinicalTrials.gov: NCT03535935) RESULTS: During the 48-week period, the estimated difference in the slope of eGFR decline was 4.6 ml/min/1.73m2 per year (95 %CI: 1.5 to 7.6, p = 0.003) slower with astragalus. For UACR, the estimated inter-group proportional difference in the slope of change was insignificant (1.14, 95 %CI: 0.85 to 1.52, p = 0.392). 117 adverse events from 31 astragalus-treated patients and 41 standard care-controlled patients were documented. The 48-week endpoint systolic blood pressure was 7.9 mmHg lower (95 %CI: -12.9 to -2.8, p = 0.003) in the astragalus-treated patients. 113 (96 %) and 107 (91 %) patients had post-randomization and endpoint primary outcome measures, respectively.
    CONCLUSIONS: In patients with type 2 diabetes, stage 2 to 3 CKD and macroalbuminuria, add-on astragalus for 48 weeks further stabilized kidney function on top of standard care.
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  • 文章类型: Journal Article
    为了完善制定中西医结合(ICWM)临床实践指南(CPG)的方法,促进诚信的形成,整合中西医优势的可实施建议。
    使用标称分组技术(NGT)方法,成立了一个多学科专家小组。小组通过文献回顾和反复讨论,确定了ICWM-CPG开发中的关键方法问题,并制定了解决这些问题的方法建议。最后一组提案是通过小组成员之间的共识达成的。
    合作努力导致确定了五个关键的方法论问题,并随后建立了22个具体建议。这些包括严格遵守著名的标准,例如医学研究所(IOM)和国际准则网络(G-I-N)提出的建议,采用诸如等级方法和正确陈述之类的方法,平衡发展集团的战略构成,以ICWM为重点的临床调查的熟练识别,不同证据来源的细微差别整合,以及透明的细节,可实施的建议。
    本研究集中于ICWM-CPG开发中最关键和最普遍的方法学问题,提出一系列建议。这些建议来自多学科专家共识,旨在为ICWM-CPG开发人员提供方法学指导,建立在当前的基础方法上。
    UNASSIGNED: To refine the methods of developing clinical practice guidelines (CPGs) for integrative Chinese-Western medicine (ICWM), promoting the formation of trustworthy, implementable recommendations that integrate the strengths of Chinese and Western medicine.
    UNASSIGNED: Using a nominal group technique (NGT) approach, a multidisciplinary expert panel was established. The panel identified key methodological issues in ICWM-CPG development through literature review and iterative discussions, and formulated methodological proposals to address these issues. The final set of proposals was achieved through consensus among the panel members.
    UNASSIGNED: The collaborative effort resulted in the identification of five pivotal methodological issues and the subsequent establishment of 22 specific recommendations. These encompass strict adherence to renowned standards, such as those proposed by the Institute of Medicine (IOM) and Guidelines International Network (G-I-N), the employment of methodologies like the GRADE approach and RIGHT statement, the strategic constitution of a balanced development group, the adept identification of ICWM-focused clinical inquiries, the nuanced integration of diverse evidence sources, and the detailed crafting of transparent, implementable recommendations.
    UNASSIGNED: This study concentrates on the most crucial and prevalent methodological issues in ICWM-CPG development, proposing a series of recommendations. These suggestions result from a multidisciplinary expert consensus, aiming to provide methodological guidance for ICWM-CPG developers, building upon the current foundational methodologies.
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  • 文章类型: Journal Article
    为了对原发性痛经最有效的针灸疗法进行比较和排名,并为该病的临床治疗提供循证医学支持。
    对中国国家知识基础设施(CNKI)进行了全面搜索,万方数据库,中文期刊信息服务平台(VIP),中国生物医学文献服务系统(中国医学),PubMed,WebofScience,Embase,和Cochrane图书馆数据库从成立到2023年5月1日。使用Cochrane协作偏差风险工具评估偏差风险,采用Stata15.1软件和R4.3.1软件的GeMTC软件包进行网络Meta分析。
    包括70项研究,包括5772例原发性痛经患者,涉及临床常用的25种针灸技术。纳入文献质量较低,他们中的大多数没有提到临床试验中心的注册信息,具体的样本量估算方法尚不清楚。一些文献没有解释具体的随机方法,分布隐蔽性和盲目性,因此存在一定的发表偏倚和小样本效应。结果表明,提高临床有效率,前三名是盐隔灸,按摩疗法+穴位敷贴,针灸+热敏灸。在降低视觉模拟量表(VAS)方面,前三名的治疗方法是按摩疗法+穴位修补,针刺+穴位贴敷和温针灸。在缓解考克斯月经症状量表(CMSS)方面,前三名是针灸+穴位贴敷,穴位修补和穴位埋线。在缓解中医症状评分方面,前三个治疗方法是穴位贴敷+热敏灸,穴位敷贴和艾灸。
    不同的针灸疗法在提高临床有效率方面比口服镇痛药更具优势,降低VAS评分,降低CMSS得分,减轻中医症状积分。其中,按摩疗法+穴位敷贴,针刺+穴位敷贴和穴位敷贴可能是治疗原发性痛经的最佳方案。然而,更多的大样本,需要多中心和高质量的随机对照试验来证明.
    UNASSIGNED: In order to compare and rank the most effective acupuncture therapy for primary dysmenorrhea and provide evidence-based medical support for clinical treatment of this disease.
    UNASSIGNED: A comprehensive search was conducted on China National Knowledge Infrastructure (CNKI), Wanfang Database, Information Chinese Journal Service Platform (VIP), China Biomedical Literature Service System (SinoMed), PubMed, Web of Science, Embase, and Cochrane Library databases from their inception to May 1, 2023. The Cochrane Collaboration Risk of Bias Tool was used to evaluate bias risk, and the GeMTC package of Stata 15.1 software and R 4.3.1 software was used to perform network Meta-analysis.
    UNASSIGNED: 70 studies were included, including 5772 patients with primary dysmenorrhea, involving 25 kinds of acupuncture techniques commonly used in clinic. The quality of the included literature was low, most of them did not mention the registration information of clinical trial centers, and the specific sample size estimation method was unclear. Some literature did not explain the specific random method, distribution concealment and blindness, so there was a certain publication bias and small sample effect. Results showed that for improving the clinical effective rate, the top three treatments were salt-separated moxibustion, massotherapy + acupoint patching, acupuncture + heat-sensitive moxibustion. In terms of reducing the visual analogue scale(VAS), the top three treatments were massotherapy + acupoint patching, acupuncture + acupoint patching and warm acupuncture. In terms of alleviating cox menstrual symptom scale (CMSS), the top three treatments were acupuncture + acupoint patching, acupoint patching and point embedding. In relieving TCM symptom score, the top three treatments were acupoint patching + heat-sensitive moxibustion, acupoint patching and moxibustion.
    UNASSIGNED: Different acupuncture therapies have more advantages than oral analgesics in improving the clinical effective rate, reducing VAS score, reducing CMSS score, and alleviating TCM symptom score. Among them, massage therapy + acupoint patching, acupuncture + acupoint patching and acupoint patching may be the best solutions for the treatment of primary dysmenorrhea. However, more large-sample, multi-center and high-quality randomized controlled trials are needed to demonstrate.
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  • 文章类型: Journal Article
    慢性疲劳是COVID-19病后的主要症状,或长COVID。我们的目的是评估传统药物的疗效和安全性,补充和中西医结合治疗COVID-19感染后疲劳。
    截至2023年4月12日,共检索了10个英文和中文数据库和灰色文献进行随机对照试验(RCT)。应用Cochrane“偏倚风险”(RoB)工具。证据确定性使用建议评估分级进行评估,发展,和评估(等级)。效果估计值表示为风险比(RR)或平均差(MD),具有95%置信区间(CI)。
    纳入了13个RCT,1632名参与者。一项RCT显示补肺活血中药胶囊减轻疲劳(n=129,MD-14.90,95CI-24.53至-5.27),一项RCT报告说,芦丹神草药液可降低疲劳(n=184,MD-1.90,95CI-2.38至-1.42),另一项RCT显示,芦丹神中药液的疲劳消失率较高(n=184,RR4.19,95CI2.06至8.53)。与单纯的中医康复(TCM-rahab)相比,一项RCT显示,清金益气颗粒加中药康复后,疲劳症状降低(n=388,MD-0.48,95CI-0.50至-0.46)。由于对RoB和/或不精确的担忧,这个证据的确定性很低到很低。未报告严重不良事件。
    有限的证据表明,各种TCIM干预措施可能会减少COVID-19后的疲劳。较大,需要持续时间较长的高质量RCT来确认这些初步发现.
    本次审查的方案已在PROSPERO:CRD420223384136注册。
    UNASSIGNED: Chronic fatigue is a predominant symptom of post COVID-19 condition, or long COVID. We aimed to evaluate the efficacy and safety of Traditional, Complementary and Integrative Medicine (TCIM) for fatigue post COVID-19 infection.
    UNASSIGNED: Ten English and Chinese language databases and grey literature were searched up to 12 April 2023 for randomized controlled trials (RCTs). Cochrane \"Risk of bias\" (RoB) tool was applied. Evidence certainty was assessed using Grading of Recommendations Assessment, Development, and Evaluation (GRADE). Effect estimates were presented as risk ratio (RR) or mean difference (MD) with 95% confidence interval (CI).
    UNASSIGNED: Thirteen RCTs with 1632 participants were included. One RCT showed that Bufei Huoxue herbal capsules reduced fatigue (n=129, MD -14.90, 95%CI -24.53 to -5.27), one RCT reported that Ludangshen herbal liquid lowered fatigue (n=184, MD -1.90, 95%CI -2.38 to -1.42), and the other one RCT shown that fatigue disappearance rate was higher with Ludangshen herbal liquid (n=184, RR 4.19, 95%CI 2.06 to 8.53). Compared to traditional Chinese medicine rehabilitation (TCM-rahab) alone, one RCT showed that fatigue symptoms were lower following Qingjin Yiqi granules plus TCM-rehab (n=388, MD -0.48, 95%CI -0.50 to -0.46). Due to concerns with RoB and/or imprecision, the certainty in this evidence was low to very low. No serious adverse events was reported.
    UNASSIGNED: Limited evidence suggests that various TCIM interventions might reduce post COVID-19 fatigue. Larger, high quality RCTs of longer duration are required to confirm these preliminary findings.
    UNASSIGNED: The protocol of this review has been registered at PROSPERO: CRD42022384136.
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  • 文章类型: Journal Article
    经皮穴位电刺激(TEAS)治疗为癌症引起的骨痛(CIBP)患者提供了家庭治疗的可能性,患者控制的疼痛管理方法。这项研究的目的是评估患者控制的TEAS(PC-TEAS)在非小细胞肺癌(NSCLC)患者中缓解CIBP的疗效。
    这是一个前瞻性的研究方案,三盲,随机对照试验。我们预计从4个中国医疗中心招募188名NSCLC骨转移患者,他们也在使用有效的阿片类镇痛药。这些参与者将以1:1的比例随机分配到真正的PC-TEAS或假PC-TEAS组。所有参与者将接受标准的肿瘤辅助治疗。真正的小组将根据需要接受患者控制的TEAS干预,而假手术组将遵循相同的治疗方案,但使用非导电凝胶贴片。每个疗程将持续7天,共管理4个课程。将有4个评估时间点:基线,第4、8和12周的结论。该研究的主要结果是治疗后第4周的简短疼痛量表(BPI)量表的平均疼痛缓解率。次要结果包括疼痛相关指标,生活质量量表,情绪量表,以及评估日的血常规.如果发生任何不良事件,将及时处理和报告。我们将使用EDC平台管理试验数据,与数据监测委员会提供定期的质量监督。
    PC-TEAS干预提供了实现家庭针灸治疗的尝试,以及在针灸研究中实现三重致盲的可行性。本研究旨在为针灸辅助治疗癌症相关性疼痛提供更严格的试验证据,并探索一种安全有效的CIBP中西医结合方案。
    ClinicalTrials.govNCT05730972,注册于2023年2月16日。
    UNASSIGNED: Transcutaneous Electrical Acupoint Stimulation (TEAS) therapy opens up the possibility for individuals with Cancer-induced bone pain (CIBP) to receive a home-based, patient-controlled approach to pain management. The aim of this study is designed to evaluate the efficacy of patient-controlled TEAS (PC-TEAS) for relieving CIBP in patients with non-small cell lung cancer (NSCLC).
    UNASSIGNED: This is a study protocol for a prospective, triple-blind, randomized controlled trial. We anticipate enrolling 188 participants with NSCLC bone metastases who are also using potent opioid analgesics from 4 Chinese medical centers. These participants will be randomly assigned in a 1:1 ratio to either the true PC-TEAS or the sham PC-TEAS group. All participants will receive standard adjuvant oncology therapy. The true group will undergo patient-controlled TEAS intervention as needed, while the sham group will follow the same treatment schedule but with non-conductive gel patches. Each treatment course will span 7 days, with a total of 4 courses administered. There will be 4 assessment time points: baseline, the conclusion of weeks 4, 8, and 12. The primary outcome of this investigation is the response rate of the average pain on the Brief Pain Inventory (BPI) scale at week 4 after treatment. Secondary outcomes include pain related indicators, quality of life scale, mood scales, and routine blood counts on the assessment days. Any adverse events will be promptly addressed and reported if they occur. We will manage trial data using the EDC platform, with a data monitoring committee providing regular quality oversight.
    UNASSIGNED: PC-TEAS interventions offer an attempt to achieve home-based acupuncture treatment and the feasibility of achieving triple blinding in acupuncture research. This study is designed to provide more rigorous trial evidence for the adjuvant treatment of cancer-related pain by acupuncture and to explore a safe and effective integrative medicine scheme for CIBP.
    UNASSIGNED: ClinicalTrials.gov NCT05730972, registered February 16, 2023.
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