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Are Supra-Physiological Plant-Based Antioxidants Ready for the Clinic? A Scoping Review of Hormetic Influences Driving Positive Clinical Outcomes. 超生理性植物抗氧化剂是否已准备好应用于临床?对推动积极临床结果的激素影响因素的范围审查。
Pub Date : 2024-02-06 eCollection Date: 2024-01-01 DOI: 10.1177/27536130241231508
Julie Wendt, Benjamin Knudsen, Leigh A Frame

Background: A pro-inflammatory metabolic state is key to the chronic disease epidemic. Clinicians' ability to use nutrients to balance inflammation via oxidant homeostasis depends on the quality of antioxidants research. Understanding the intersection of two prominent theories for how antioxidants quell inflammation-nutritional hormesis and oxidant scavenging-will enable therapeutic antioxidant use in clinical practice. Purpose: We sought to survey the literature to answer the question: has the hormetic response of exogenous antioxidants been studied in humans and if so, what is its effect Research Design: This review investigates the less well-established theory, nutritional hormesis. To understand the state of hormetic response research, we conducted a literature review describing the relationship between exogenous antioxidants, hormesis, and chronic disease. We used an adaptive search strategy (PubMed and Scopus), retrieving 343 articles, of which 218 were unique. Most studies reviewed the hormetic response in plant and cell models (73.6%) while only 2.2% were in humans. Results: Given the limited robust evidence, clinicians lack research-based guidance on the appropriate therapeutic dose of exogenous antioxidants or, more concerning, supra-physiological dosing via supplements. A critical hurdle in searching the literature is the lack of standardized nomenclature describing the hormetic effect, challenging the ability of clinicians to make informed decisions. Conclusion: Non-human research shows a biphasic, hormetic relationship with antioxidants but observational studies have yet to translate this into the complexities of human biochemistry and physiology. Therefore, we cannot accurately translate this into clinical care. To remedy this insufficiency, we suggest: (1) Improved data collection quality: controlled diet, standardized antioxidant measurements, bioavailability assessed via biomarkers; (2) Larger, harmonized datasets: research subject transparency, keyword standardization, consensus on a hormesis definition.

背景:促炎症代谢状态是慢性疾病流行的关键。临床医生利用营养素通过氧化剂平衡来平衡炎症的能力取决于抗氧化剂研究的质量。了解抗氧化剂如何抑制炎症的两个重要理论--营养激素作用和氧化剂清除作用--的交叉点将有助于在临床实践中使用抗氧化剂进行治疗。目的:我们试图通过文献调查来回答以下问题:是否在人体中研究过外源性抗氧化剂的荷尔蒙反应,如果研究过,其效果如何?这篇综述调查了营养荷尔蒙作用这一不太成熟的理论。为了了解激素反应研究的现状,我们对描述外源性抗氧化剂、激素作用和慢性疾病之间关系的文献进行了综述。我们采用了适应性检索策略(PubMed 和 Scopus),检索到 343 篇文章,其中 218 篇为唯一文章。大多数研究(73.6%)回顾了植物和细胞模型中的激素反应,只有 2.2% 的研究涉及人类。研究结果由于有力的证据有限,临床医生在外源性抗氧化剂的适当治疗剂量方面缺乏基于研究的指导,更令人担忧的是通过补充剂进行超生理剂量的治疗。检索文献的一个关键障碍是缺乏描述激素效应的标准化术语,这对临床医生做出明智决定的能力提出了挑战。结论非人类研究表明,抗氧化剂与荷尔蒙有双相关系,但观察性研究尚未将其转化为复杂的人体生物化学和生理学。因此,我们无法准确地将其转化为临床治疗。为弥补这一不足,我们建议:(1) 提高数据收集质量:控制饮食、标准化抗氧化剂测量、通过生物标志物评估生物利用率;(2) 建立更大的、统一的数据集:研究对象透明化、关键词标准化、就激素作用的定义达成共识。
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引用次数: 0
Integrative Health Equity: Definition, Principles, Strategies, and Reflections. 综合健康公平:定义、原则、策略和思考。
Pub Date : 2024-02-06 eCollection Date: 2024-01-01 DOI: 10.1177/27536130241231911
Maria T Chao, Shelley R Adler

In this viewpoint, we define integrative health equity as optimal health for all through a whole-person approach that explicitly recognizes cultural, social, and structural determinants of health. We describe seven guiding principles, along with organizational goals, strategies, and reflections to advance integrative health equity.

在本观点中,我们将 "综合健康公平 "定义为通过全人方法,明确承认健康的文化、社会和结构性决定因素,为所有人提供最佳健康。我们介绍了七项指导原则,以及推进综合健康公平的组织目标、战略和反思。
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引用次数: 0
Integrating a Community Advisory Board Into a Pragmatic Trial of Mindfulness for Chronic Low Back Pain. 将社区咨询委员会纳入 "正念治疗慢性腰痛 "的实用性试验中。
Pub Date : 2024-02-05 eCollection Date: 2024-01-01 DOI: 10.1177/27536130241231736
Natalia E Morone, Elondra D Harr, Jose E Baez, Ruth D Rodriguez, Suzanne M Lawrence, Jessica L Barnhill, Isabel Roth

Background: To improve the implementation of clinical trial interventions, there is a need to facilitate communication between key stakeholders and research teams. Community Advisory Boards (CAB) bring together a range of stakeholders not historically included in the research process to inform and work collaboratively with research teams.

Objective: To describe our procedures and processes for (1) integration of a CAB into a pragmatic clinical trial of a telehealth-delivered group mindfulness program for persons with chronic low back pain (cLBP) within primary care, and (2) for the rapid uptake and implementation of CAB recommendations.

Methods: The CAB we convened includes persons with cLBP who have undergone the mindfulness intervention, health care system leadership, advocacy groups, and mindfulness experts. The CAB members underwent a two hour initial training that introduced the research process and the CAB's role as research partners. The CAB met monthly for 1 hour. We used the Lighting Report method to summarize meetings and share feedback with the research team.

Results: The recommendations of the CAB during the first year they met were divided into recruitment, informed consent, and survey recommendations. The study website also was overhauled based on recommendations, including a more engaging first page with rotating images of nature and testimonials. The language on the website was edited to be more concise and participant-friendly. The CAB recommended talking points to discuss with participants during screening or informed consent about the benefits of participating in research.

Conclusion: We established a CAB that represented diverse perspectives, organizations, and experience with cLBP and mindfulness. The differing perspectives of the CAB resulted in recommendations that the research team itself would not have decided on their own. The Lightning Reports were also an effective way to efficiently communicate the CAB recommendations to the research team.

背景:为改善临床试验干预措施的实施,需要促进主要利益相关者与研究团队之间的沟通。社区咨询委员会(CAB)汇集了一系列历来未被纳入研究过程的利益相关者,为研究团队提供信息并与之合作:描述我们在以下方面的程序和过程:(1)将社区咨询委员会纳入针对初级保健中的慢性腰背痛(cLBP)患者的远程医疗团体正念计划的实用临床试验;(2)快速采纳和实施社区咨询委员会的建议:我们召集的正念咨询委员会成员包括接受过正念干预的慢性腰背痛患者、医疗保健系统领导、倡导团体和正念专家。CAB 成员接受了两小时的初步培训,培训内容包括研究过程和 CAB 作为研究合作伙伴的角色。咨询委员会每月召开一次会议,每次一小时。我们采用照明报告法对会议进行总结,并与研究团队分享反馈意见:CAB 在第一年会议上提出的建议分为招募建议、知情同意建议和调查建议。研究网站也根据建议进行了全面改版,包括一个更吸引人的首页,上面有自然和推荐的旋转图片。网站上的语言经过编辑,更加简洁,对参与者更加友好。CAB 建议在筛选或知情同意时与参与者讨论参与研究的益处:我们成立的心理咨询委员会代表了不同的观点、组织以及在 cLBP 和正念方面的经验。CAB 的不同观点产生了研究团队自己无法决定的建议。闪电报告 "也是向研究团队有效传达咨询委员会建议的有效方式。
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引用次数: 0
Biofield Therapies: Guidelines for Reporting Clinical Trials. 生物场疗法:临床试验报告指南》。
Pub Date : 2024-01-31 eCollection Date: 2024-01-01 DOI: 10.1177/27536130231202501
Richard Hammerschlag, Meredith Sprengel, Ann L Baldwin

A set of guidelines has been developed to help improve reporting of clinical trials of biofield therapies. The need for enhanced transparency when reporting trials of this family of integrative health practices, eg, External Qigong, Healing Touch, Reiki and Therapeutic Touch, has been advocated in systematic reviews of these studies. The guidelines, called Biofield Therapies: Reporting Evidence Guidelines (BiFi REGs), supplement CONsolidated Standards of Reporting Trials (CONSORT) 2010 by including details of the intervention protocols relevant to biofield therapy trials. BiFi REGs evolved through a draft document created by a core group, two rounds of a Delphi process with an international group of subject matter experts and two panels, meeting via Zoom, which included editors of complementary and integrative medicine journals. BiFi REGs comprises a 15-item Intervention checklist. Modifications of two other CONSORT topic areas are also proposed to enhance their relevance to trials of biofield therapies. Included for each item are an explanation, and exemplars of reporting from peer-reviewed published reports of biofield therapy trials. When used in conjunction with all other items from CONSORT 2010, we anticipate that BiFi REGs will expedite the peer review process for biofield therapy trials, facilitate attempts at trial replication and help to inform decision-making in the clinical practice of biofield therapies.

为帮助改进生物场疗法临床试验的报告工作,我们制定了一套指南。在对这一系列综合保健实践(如外气功、抚触疗法、灵气疗法和治疗性抚触疗法)的研究进行系统回顾时,一直提倡在报告这些试验时需要提高透明度。该指南名为《生物场疗法:报告证据指南》(BiFi REGs)是对《2010 年试验报告标准》(CONSORT)的补充,其中包括与生物场疗法试验相关的干预方案细节。BiFi REGs 是由一个核心小组起草文件、与国际主题专家小组进行两轮德尔菲程序以及通过 Zoom 会议的两个专家小组(其中包括补充医学和综合医学期刊的编辑)共同制定的。BiFi REGs 包括一个 15 个项目的干预检查表。此外,还建议对 CONSORT 的其他两个主题领域进行修改,以增强其与生物场疗法试验的相关性。每个项目都包含解释,以及经同行评审的生物场疗法试验报告范例。如果与 CONSORT 2010 中的所有其他项目结合使用,我们预计 BiFi REGs 将加快生物场疗法试验的同行评审过程,促进试验复制的尝试,并有助于为生物场疗法临床实践中的决策提供信息。
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引用次数: 0
Evaluation of a Guided Nature and Forest Therapy Walk for Internal Medical Residents - A Brief Report. 针对内科住院医师的自然与森林疗法徒步旅行指导评估--简要报告。
Pub Date : 2024-01-17 eCollection Date: 2024-01-01 DOI: 10.1177/27536130241228181
Katherine T Morrison, Kristin M Jensen, Angela Keniston, Lauren McBeth, Amber L Vermeesch, Kerry Nellie O'Connor

Background: Medical residents commonly face compassion fatigue, burnout, anxiety, and depression. Studies of nature-based interventions show improved mental and physical health; few focus on healthcare providers.

Objective: To explore potential benefits of forest bathing for medical residents' wellbeing.

Methods: Using the Association of Nature and Forest Therapy's framework, we piloted a forest bathing intervention among medical residents with pre/post-participation surveys assessing perceptions of mindfulness and psychological wellbeing. Responses were analyzed using a Fisher's exact test and Student's t-test for independent samples.

Results: Fourteen of fifteen participants completed both surveys. We observed significantly improved mindfulness scores and expressions of feeling calm, vital, or creative, as well as a decreased sense of anxiety and depression. Nonsignificant trends towards decreased burnout and irritability were seen.

Conclusion: This quality improvement pilot demonstrates trends that forest bathing can improve medical residents' psychological wellbeing and mindfulness. Further exploration of this intervention for healthcare providers is warranted.

背景:医学住院医师普遍面临同情疲劳、职业倦怠、焦虑和抑郁等问题。有关基于自然的干预措施的研究显示,心理和身体健康得到了改善;但很少有研究关注医疗服务提供者:探索森林浴对住院医生健康的潜在益处:利用自然与森林疗法协会的框架,我们在医疗住院医师中试行了森林浴干预措施,并对参与前后的调查进行了评估,以了解他们对正念和心理健康的看法。采用费雪精确检验和学生 t 检验对独立样本进行分析:15 名参与者中有 14 人完成了这两项调查。我们观察到,参与者的正念得分和对平静、活力或创造力的感受明显提高,焦虑感和抑郁感也有所下降。倦怠感和烦躁感的下降趋势并不明显:这项质量改进试点项目表明,森林浴可以改善住院医师的心理健康和正念。有必要进一步探索这种针对医疗服务提供者的干预措施。
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引用次数: 0
Validation of Blood Glucose and Lipid-Lowering Effect of Solvent Fractions of the Crinum Abyssinicum Shoot Tips in Streptozotocin-Induced Diabetic Mice. 验证 Crinum Abyssinicum 射梢溶剂馏分对链脲佐菌素诱导的糖尿病小鼠的降血糖和降血脂作用
Pub Date : 2024-01-13 eCollection Date: 2024-01-01 DOI: 10.1177/27536130231225464
Bantayehu Addis Tegegne, Wubetu Yihunie, Yibeltal Aschale, Habtamu Belew, Melese Getachew

Background: Diabetes mellitus prevalence has reached epidemic levels despite the existence of contemporary treatments. People thus started looking at the possible therapeutic value of natural therapies. Crushed shoot tips of Crinum abyssinicum (Amaryllidaceae) are mixed with water in Ethiopia to treat diabetes, yet this practice is not well supported by science.

Objective: In this experiment, mice models were used to verify the blood sugar and lipid-lowering benefits of solvent fractions of C. abyssinicum shoot tips.

Materials and methods: In a single-dose treated Streptozotocin (STZ)-induced diabetic model, mice were randomly grouped into eleven categories which include diabetic negative control, diabetic positive control, and 9 diabetic treatment groups. In repeated daily doses treated STZ-induced model, Mice were divided into 6 groups which included normal and diabetic negative control (TW80), diabetic positive control (5 mg/kg glibenclamide), and three diabetic treatment groups 100, 200, and 400 mg/kg). Finally, blood glucose, lipid level, and body weight were examined.

Results: In the single-dose treated diabetic model, there was a significant blood glucose reduction at 200 and 400 mg/kg doses of aqueous fraction and glibenclamide starting from the sixth-hour post-administration unlike ethyl acetate and chloroform fraction compared to baseline and negative control. In repeated daily dose-treated diabetic mice, all three doses (100, 200, and 400 mg/kg of aqueous fraction) resulted in a substantial reduction (P < .001) in blood glucose compared to baseline and negative control on the seventh day and 14th day. Besides the AQF shows improvement in lipid levels and body weight parameters.

Conclusion: The results of the study demonstrated that C. abyssinicum shoot tip fractions have the greatest potential to lower blood sugar and lipid levels, supporting conventional claims for the treatment of diabetes.

背景:尽管有现代治疗方法,但糖尿病的发病率已达到流行病的水平。因此,人们开始关注自然疗法的可能治疗价值。在埃塞俄比亚,人们将阿比西尼亚蟋蟀(Amaryllidaceae)的嫩枝梢捣碎后与水混合来治疗糖尿病,但这种做法并没有得到科学的支持:本实验使用小鼠模型来验证 C. abyssinicum 嫩枝尖溶剂馏分的降血糖和降血脂功效:在单剂量治疗链脲佐菌素(STZ)诱导的糖尿病模型中,将小鼠随机分为 11 组,包括糖尿病阴性对照组、糖尿病阳性对照组和 9 个糖尿病治疗组。在每日重复剂量治疗 STZ 诱导的模型中,小鼠被分为 6 组,包括正常和糖尿病阴性对照组(TW80)、糖尿病阳性对照组(5 毫克/千克格列本脲)和 3 个糖尿病治疗组(100、200 和 400 毫克/千克)。最后,对血糖、血脂水平和体重进行了检测:结果:在单剂量治疗的糖尿病模型中,与基线和阴性对照组相比,200 和 400 毫克/千克剂量的水馏分和格列本脲从给药后第六小时开始血糖显著降低,而乙酸乙酯和氯仿馏分则不同。在每天重复给药的糖尿病小鼠中,与基线和阴性对照组相比,所有三种剂量(100、200 和 400 毫克/千克水溶液馏分)在给药后第七天和第 14 天的血糖都有显著降低(P < .001)。此外,AQF 还改善了血脂水平和体重参数:研究结果表明,C. abyssinicum嫩枝尖馏分具有降低血糖和血脂水平的最大潜力,支持治疗糖尿病的传统说法。
{"title":"Validation of Blood Glucose and Lipid-Lowering Effect of Solvent Fractions of the <i>Crinum Abyssinicum</i> Shoot Tips in Streptozotocin-Induced Diabetic Mice.","authors":"Bantayehu Addis Tegegne, Wubetu Yihunie, Yibeltal Aschale, Habtamu Belew, Melese Getachew","doi":"10.1177/27536130231225464","DOIUrl":"10.1177/27536130231225464","url":null,"abstract":"<p><strong>Background: </strong>Diabetes mellitus prevalence has reached epidemic levels despite the existence of contemporary treatments. People thus started looking at the possible therapeutic value of natural therapies. Crushed shoot tips of <i>Crinum abyssinicum</i> (Amaryllidaceae) are mixed with water in Ethiopia to treat diabetes, yet this practice is not well supported by science.</p><p><strong>Objective: </strong>In this experiment, mice models were used to verify the blood sugar and lipid-lowering benefits of solvent fractions of <i>C. abyssinicum</i> shoot tips.</p><p><strong>Materials and methods: </strong>In a single-dose treated Streptozotocin (STZ)-induced diabetic model, mice were randomly grouped into eleven categories which include diabetic negative control, diabetic positive control, and 9 diabetic treatment groups. In repeated daily doses treated STZ-induced model, Mice were divided into 6 groups which included normal and diabetic negative control (TW80), diabetic positive control (5 mg/kg glibenclamide), and three diabetic treatment groups 100, 200, and 400 mg/kg). Finally, blood glucose, lipid level, and body weight were examined.</p><p><strong>Results: </strong>In the single-dose treated diabetic model, there was a significant blood glucose reduction at 200 and 400 mg/kg doses of aqueous fraction and glibenclamide starting from the sixth-hour post-administration unlike ethyl acetate and chloroform fraction compared to baseline and negative control. In repeated daily dose-treated diabetic mice, all three doses (100, 200, and 400 mg/kg of aqueous fraction) resulted in a substantial reduction (<i>P</i> < .001) in blood glucose compared to baseline and negative control on the seventh day and 14<sup>th</sup> day. Besides the AQF shows improvement in lipid levels and body weight parameters.</p><p><strong>Conclusion: </strong>The results of the study demonstrated that <i>C. abyssinicum</i> shoot tip fractions have the greatest potential to lower blood sugar and lipid levels, supporting conventional claims for the treatment of diabetes.</p>","PeriodicalId":73159,"journal":{"name":"Global advances in integrative medicine and health","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10788077/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139473151","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Yoga Plus Mantram Repetition to Reduce Chronic Pain in Veterans With Post-Traumatic Stress Disorder: A Feasibility Trial. 重复练习瑜伽和咒语以减轻患有创伤后应激障碍的退伍军人的慢性疼痛:可行性试验。
Pub Date : 2023-12-26 eCollection Date: 2023-01-01 DOI: 10.1177/27536130231220623
Erik J Groessl, Carol Hafey, Adhana McCarthy, Rahil M Hernandez, Miguel Prado-Nava, Danielle Casteel, Symone McKinnon, Douglas G Chang, Catherine R Ayers, Thomas R Rutledge, Ariel J Lang, Jill E Bormann

Background: Veterans with post-traumatic stress disorder (PTSD) are more likely to report chronic pain than veterans without PTSD. Yoga has been shown to reduce both chronic pain and PTSD symptoms in clinical trials. The goal of our study was to assess the feasibility and acceptability of conducting a randomized controlled trial (RCT) that combined yoga and mantram repetition (Yoga + MR) into one program for military veterans with both chronic pain and PTSD.

Methods: In this feasibility RCT, 27 veterans were randomized to either Yoga + MR or a relaxation intervention. Due to the COVID-19 pandemic, in-person recruitment, assessments, and intervention attendance were re-evaluated. Although remote delivery of aspects of the study were utilized, interventions were delivered in-person. Feasibility benchmarks met included full recruitment in 12 months or less, 75%+ retention at initial follow-up assessment, 50%+ attendance rate, and 75%+ of participants satisfied with the interventions.

Results: The sample was racially and ethnically diverse, and 15% of participants were women. Participant recruitment lasted approximately 11 months. Out of 32 participants initially randomized, two participants asked to be dropped from the study and three did not meet PTSD symptom criteria. For the remaining 27 participants, retention rates were 85% at 12 weeks and 81% at 18 weeks. Participants attended 66% of in-person yoga and 55% of in-person relaxation sessions. Satisfaction was high, with 100% of yoga participants and 75%/88% of relaxation participants agreeing or strongly agreeing they were satisfied with the intervention/instructors. After 12 weeks (end of intervention), Yoga + MR participants reported reduced back-pain related disability (primary outcome), reduced alcohol use, reduced fatigue, and increased quality of life, while relaxation group participants reported reductions in pain severity, PTSD symptoms, and fatigue.

Conclusions: Amidst many research challenges during the pandemic, recruitment, retention, and efficacy results from this feasibility trial support advancement to a larger RCT to study Yoga + MR for chronic pain and PTSD.

背景:与没有创伤后应激障碍(PTSD)的退伍军人相比,患有创伤后应激障碍(PTSD)的退伍军人更有可能报告慢性疼痛。临床试验表明,瑜伽可以减轻慢性疼痛和创伤后应激障碍症状。我们研究的目的是评估开展随机对照试验(RCT)的可行性和可接受性,该试验将瑜伽和曼陀罗重复练习(瑜伽+曼陀罗)结合为一项计划,用于患有慢性疼痛和创伤后应激障碍的退伍军人:在这项可行性 RCT 试验中,27 名退伍军人被随机分配到瑜伽+MR 或放松干预项目中。由于 COVID-19 大流行,对亲自招募、评估和干预出席情况进行了重新评估。虽然研究的某些方面采用了远程交付,但干预仍是面对面进行的。达到的可行性基准包括:在 12 个月或更短时间内完成全部招募工作、在首次随访评估中保留 75% 以上的参与者、50% 以上的出席率以及 75% 以上的参与者对干预措施表示满意:样本具有种族和民族多样性,15% 的参与者为女性。参与者招募持续了约 11 个月。在最初随机抽取的 32 名参与者中,有 2 人要求退出研究,3 人不符合创伤后应激障碍症状标准。剩下的 27 名参与者中,12 周的保留率为 85%,18 周的保留率为 81%。参与者参加了 66% 的现场瑜伽课程和 55% 的现场放松课程。满意度很高,100% 的瑜伽参与者和 75%/88% 的放松参与者同意或非常同意他们对干预措施/指导者感到满意。12 周后(干预结束),"瑜伽+ MR "参与者报告称,与背部疼痛有关的残疾(主要结果)减少了,饮酒减少了,疲劳减少了,生活质量提高了,而放松组参与者报告称,疼痛严重程度、创伤后应激障碍症状和疲劳减少了:结论:在大流行病期间,研究工作面临诸多挑战,但这项可行性试验的招募、保留和疗效结果都支持推进更大规模的 RCT 研究,研究瑜伽 + MR 对慢性疼痛和创伤后应激障碍的治疗效果。
{"title":"Yoga Plus Mantram Repetition to Reduce Chronic Pain in Veterans With Post-Traumatic Stress Disorder: A Feasibility Trial.","authors":"Erik J Groessl, Carol Hafey, Adhana McCarthy, Rahil M Hernandez, Miguel Prado-Nava, Danielle Casteel, Symone McKinnon, Douglas G Chang, Catherine R Ayers, Thomas R Rutledge, Ariel J Lang, Jill E Bormann","doi":"10.1177/27536130231220623","DOIUrl":"10.1177/27536130231220623","url":null,"abstract":"<p><strong>Background: </strong>Veterans with post-traumatic stress disorder (PTSD) are more likely to report chronic pain than veterans without PTSD. Yoga has been shown to reduce both chronic pain and PTSD symptoms in clinical trials. The goal of our study was to assess the feasibility and acceptability of conducting a randomized controlled trial (RCT) that combined yoga and mantram repetition (Yoga + MR) into one program for military veterans with both chronic pain and PTSD.</p><p><strong>Methods: </strong>In this feasibility RCT, 27 veterans were randomized to either Yoga + MR or a relaxation intervention. Due to the COVID-19 pandemic, in-person recruitment, assessments, and intervention attendance were re-evaluated. Although remote delivery of aspects of the study were utilized, interventions were delivered in-person. Feasibility benchmarks met included full recruitment in 12 months or less, 75%+ retention at initial follow-up assessment, 50%+ attendance rate, and 75%+ of participants satisfied with the interventions.</p><p><strong>Results: </strong>The sample was racially and ethnically diverse, and 15% of participants were women. Participant recruitment lasted approximately 11 months. Out of 32 participants initially randomized, two participants asked to be dropped from the study and three did not meet PTSD symptom criteria. For the remaining 27 participants, retention rates were 85% at 12 weeks and 81% at 18 weeks. Participants attended 66% of in-person yoga and 55% of in-person relaxation sessions. Satisfaction was high, with 100% of yoga participants and 75%/88% of relaxation participants agreeing or strongly agreeing they were satisfied with the intervention/instructors. After 12 weeks (end of intervention), Yoga + MR participants reported reduced back-pain related disability (primary outcome), reduced alcohol use, reduced fatigue, and increased quality of life, while relaxation group participants reported reductions in pain severity, PTSD symptoms, and fatigue.</p><p><strong>Conclusions: </strong>Amidst many research challenges during the pandemic, recruitment, retention, and efficacy results from this feasibility trial support advancement to a larger RCT to study Yoga + MR for chronic pain and PTSD.</p>","PeriodicalId":73159,"journal":{"name":"Global advances in integrative medicine and health","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10752061/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139049860","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Healthcare Professionals' Perspectives on Improving Dietary Supplement Documentation in the Electronic Medical Record: Current Challenges and Opportunities to Enhance Quality of Care and Patient Safety. 医疗保健专业人员对改进电子病历中膳食补充剂文档的看法:提高医疗质量和患者安全的当前挑战与机遇》(Current Challenges and Opportunities to Enhance of Quality of Care and Patient Safety.
Pub Date : 2023-12-19 eCollection Date: 2023-01-01 DOI: 10.1177/27536130231215029
Zachary O Kadro, Aisha Chilcoat, Jacob Hill, Stephanie Kenney, Catharine Nguyen, Elana Post, Amanda H Corbett, Gary N Asher, Keturah Faurot

Background: Around half the US population uses dietary supplements (DS), and concomitant use with medications is common. Many DS include bioactive substances that can interact with medications; therefore, accurate tracking is critical for patient safety. Unfortunately, documentation of patients' DS use is often missing or incomplete in the electronic medical record (EMR), leaving patients susceptible to potential adverse events. Novel approaches to assist healthcare professionals (HCPs) in capturing patients' DS use are needed.

Objective: To assess HCPs' perspectives on challenges and facilitators of DS documentation in the EMR and their opinions on a proposed mHealth application (app) to aid in DS capture.

Methods: HCPs, recruited from professional networks, largely in North Carolina, using purposive sampling, took part in semi-structured interviews. We inquired about HCPs' experiences with DS documentation in the EMR and their opinions about our proposed mHealth app. Interviews were recorded, transcribed, and coded. Thematic analysis included deductive codes based on the interview guide, and inductive codes that emerged during transcript review.

Results: HCPs (N = 30) included 60% females, mean age 46 ± 10; 70% White. Pharmacists (20%), nurses (17%), and physicians (17%) were the most represented professions. Years in practice ranged from 3-35 years. Most HCPs were concerned about DS safety and potential supplement-drug interactions, and cited several barriers to accurate EMR DS documentation including time constraints, database inconsistencies, and poor patient-HCP communication about DS. HCPs' views on our proposed mHealth app were generally positive. They expressed that our proposed mHealth app could streamline documentation processes and enhance patient-provider communication. HCPs expressed desire for a high-quality mHealth app that includes access to evidence-based DS information, integrates with the EMR, and does not increase time burdens.

Conclusion: HCPs believe documentation of patients' DS use is important but not accurately captured in the EMR. Support was expressed for our proposed barcode-scanning DS mHealth app.

背景:美国约有一半人口使用膳食补充剂(DS),与药物同时使用的情况很普遍。许多膳食补充剂都含有可与药物发生相互作用的生物活性物质;因此,准确追踪对患者安全至关重要。遗憾的是,电子病历(EMR)中关于患者使用保健品的记录往往缺失或不完整,导致患者很容易发生潜在的不良事件。我们需要新的方法来帮助医护人员(HCPs)记录患者使用 DS 的情况:评估医护人员对在 EMR 中记录 DS 所面临的挑战和促进因素的看法,以及他们对拟议的移动医疗应用程序(App)的意见,以帮助采集 DS。方法:采用目的性抽样,从专业网络(主要在北卡罗来纳州)招募的医护人员参加了半结构化访谈。我们询问了 HCPs 在 EMR 中记录 DS 的经验以及他们对我们提议的移动医疗应用程序的意见。我们对访谈进行了记录、转录和编码。主题分析包括基于访谈指南的演绎编码和在审阅记录誊本时出现的归纳编码:高级保健人员(N = 30)中女性占 60%,平均年龄为 46 ± 10 岁;白人占 70%。药剂师(20%)、护士(17%)和医生(17%)是占比最多的职业。从业年限在 3-35 年之间。大多数保健医生都对 DS 安全性和潜在的补充剂与药物之间的相互作用表示担忧,并列举了准确记录 EMR DS 的几个障碍,包括时间限制、数据库不一致以及患者与保健医生之间关于 DS 的沟通不畅。保健医生对我们建议的移动医疗应用程序的看法普遍积极。他们表示,我们建议的移动医疗应用程序可以简化记录流程,加强患者与医疗服务提供者之间的沟通。医疗保健人员表示希望获得一款高质量的移动医疗应用程序,其中包括获取以证据为基础的 DS 信息、与 EMR 集成以及不增加时间负担:HCPs 认为记录患者使用 DS 的情况非常重要,但 EMR 并未准确记录。他们对我们提出的条形码扫描 DS 移动医疗应用程序表示支持。
{"title":"Healthcare Professionals' Perspectives on Improving Dietary Supplement Documentation in the Electronic Medical Record: Current Challenges and Opportunities to Enhance Quality of Care and Patient Safety.","authors":"Zachary O Kadro, Aisha Chilcoat, Jacob Hill, Stephanie Kenney, Catharine Nguyen, Elana Post, Amanda H Corbett, Gary N Asher, Keturah Faurot","doi":"10.1177/27536130231215029","DOIUrl":"10.1177/27536130231215029","url":null,"abstract":"<p><strong>Background: </strong>Around half the US population uses dietary supplements (DS), and concomitant use with medications is common. Many DS include bioactive substances that can interact with medications; therefore, accurate tracking is critical for patient safety. Unfortunately, documentation of patients' DS use is often missing or incomplete in the electronic medical record (EMR), leaving patients susceptible to potential adverse events. Novel approaches to assist healthcare professionals (HCPs) in capturing patients' DS use are needed.</p><p><strong>Objective: </strong>To assess HCPs' perspectives on challenges and facilitators of DS documentation in the EMR and their opinions on a proposed mHealth application (app) to aid in DS capture.</p><p><strong>Methods: </strong>HCPs, recruited from professional networks, largely in North Carolina, using purposive sampling, took part in semi-structured interviews. We inquired about HCPs' experiences with DS documentation in the EMR and their opinions about our proposed mHealth app. Interviews were recorded, transcribed, and coded. Thematic analysis included deductive codes based on the interview guide, and inductive codes that emerged during transcript review.</p><p><strong>Results: </strong>HCPs (N = 30) included 60% females, mean age 46 ± 10; 70% White. Pharmacists (20%), nurses (17%), and physicians (17%) were the most represented professions. Years in practice ranged from 3-35 years. Most HCPs were concerned about DS safety and potential supplement-drug interactions, and cited several barriers to accurate EMR DS documentation including time constraints, database inconsistencies, and poor patient-HCP communication about DS. HCPs' views on our proposed mHealth app were generally positive. They expressed that our proposed mHealth app could streamline documentation processes and enhance patient-provider communication. HCPs expressed desire for a high-quality mHealth app that includes access to evidence-based DS information, integrates with the EMR, and does not increase time burdens.</p><p><strong>Conclusion: </strong>HCPs believe documentation of patients' DS use is important but not accurately captured in the EMR. Support was expressed for our proposed barcode-scanning DS mHealth app.</p>","PeriodicalId":73159,"journal":{"name":"Global advances in integrative medicine and health","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10734342/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138833354","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Web-Based Mind-Body Intervention (Mindful Steps) for Promoting Walking in Chronic Cardiopulmonary Disease: Insights From a Qualitative Study. 基于网络的身心干预(正念步骤)促进慢性心肺疾病患者步行:来自定性研究的见解。
Pub Date : 2023-12-02 eCollection Date: 2023-01-01 DOI: 10.1177/27536130231212169
Kristen M Kraemer, Karen Kilgore, Daniel Litrownik, Brianna Jean-Laurent, Peter M Wayne, Caroline R Richardson, Marilyn L Moy, Gloria Y Yeh

Background: Given the deleterious effects of physical inactivity in persons with chronic obstructive pulmonary disease (COPD) and/or heart failure (HF), interventions that promote long-term daily physical activity are needed. Mindful Steps, designed to promote walking behaviors in COPD and HF, is a multicomponent intervention that integrates mind-body content with other self-regulatory components. The aim of the current qualitative study was to characterize participants' experiences with Mindful Steps and understand the perceived influence of the intervention on walking and health.

Method: In the context of a pilot randomized controlled feasibility trial comparing the year-long Mindful Steps program to usual care among individuals with COPD and HF, semi-structured qualitative interviews were administered at 6- and 12-months. Interviews were audio recorded and transcribed. The constant comparative method was used to code transcripts, identify categories, and develop interrelated themes.

Results: Nineteen participants (63% female; Mage = 70.2 years, SD = 6.95) who were randomized to the intervention group completed the 6-month interview and 17 completed the 12-month interview. The pedometer with feedback, live group classes, and mind-body videos were described as the most helpful intervention components. Participants learned several strategies that helped their walking (e.g., breathing regulation and awareness, body awareness, mind-body techniques, pacing), described walking as enjoyable, and identified internal reasons for walking (e.g., to feel good). They also reported several physical and mental health benefits of the intervention. Some participants reported limited influence of the intervention on walking or health. Many participants continued to use the strategies they learned in the first half of the intervention at 12-months.

Conclusions: The mind-body content of Mindful Steps appeared to positively influence walking behaviors. Participants' experiences with the intervention helped to identify areas for future intervention refinement. Future quantitative work is needed to corroborate these qualitative findings and assess the efficacy of the intervention on long-term physical activity engagement.

Trial registration: This trial is registered in Clinical Trials.gov, ID number NCT01551953.

背景:考虑到慢性阻塞性肺疾病(COPD)和/或心力衰竭(HF)患者缺乏身体活动的有害影响,促进长期日常身体活动的干预措施是必要的。正念步骤,旨在促进COPD和HF患者的步行行为,是一种多成分干预,将身心内容与其他自我调节成分相结合。当前定性研究的目的是描述参与者的正念步法体验,并了解干预对步行和健康的感知影响。方法:在一项随机对照可行性试验的背景下,对慢性阻塞性肺病和心力衰竭患者进行为期一年的正念步骤计划与常规护理进行比较,在6个月和12个月时进行半结构化定性访谈。采访录音和文字记录。经常比较的方法被用来编码转录本,确定类别,并发展相互关联的主题。结果:19名参与者(63%为女性;年龄= 70.2岁,SD = 6.95),随机分为干预组,完成6个月的随访,17例完成12个月的随访。带反馈的计步器、现场小组课程和身心视频被认为是最有帮助的干预成分。参与者学习了几种有助于步行的策略(例如,呼吸调节和意识,身体意识,身心技巧,节奏),将步行描述为愉快的,并确定步行的内在原因(例如,感觉良好)。他们还报告了这种干预对身体和心理健康的一些好处。一些参与者报告说,干预对步行或健康的影响有限。许多参与者在12个月时继续使用他们在干预的前半段学到的策略。结论:正念步法的身心内容对步行行为有积极影响。参与者在干预方面的经验有助于确定未来干预改进的领域。未来的定量工作需要证实这些定性研究结果,并评估干预对长期体育活动参与的效果。试验注册:该试验已在Clinical Trials.gov注册,ID号NCT01551953。
{"title":"A Web-Based Mind-Body Intervention (Mindful Steps) for Promoting Walking in Chronic Cardiopulmonary Disease: Insights From a Qualitative Study.","authors":"Kristen M Kraemer, Karen Kilgore, Daniel Litrownik, Brianna Jean-Laurent, Peter M Wayne, Caroline R Richardson, Marilyn L Moy, Gloria Y Yeh","doi":"10.1177/27536130231212169","DOIUrl":"10.1177/27536130231212169","url":null,"abstract":"<p><strong>Background: </strong>Given the deleterious effects of physical inactivity in persons with chronic obstructive pulmonary disease (COPD) and/or heart failure (HF), interventions that promote long-term daily physical activity are needed. Mindful Steps, designed to promote walking behaviors in COPD and HF, is a multicomponent intervention that integrates mind-body content with other self-regulatory components. The aim of the current qualitative study was to characterize participants' experiences with Mindful Steps and understand the perceived influence of the intervention on walking and health.</p><p><strong>Method: </strong>In the context of a pilot randomized controlled feasibility trial comparing the year-long Mindful Steps program to usual care among individuals with COPD and HF, semi-structured qualitative interviews were administered at 6- and 12-months. Interviews were audio recorded and transcribed. The constant comparative method was used to code transcripts, identify categories, and develop interrelated themes.</p><p><strong>Results: </strong>Nineteen participants (63% female; <i>M</i><sub><i>age</i></sub> = 70.2 years, <i>SD</i> = 6.95) who were randomized to the intervention group completed the 6-month interview and 17 completed the 12-month interview. The pedometer with feedback, live group classes, and mind-body videos were described as the most helpful intervention components. Participants learned several strategies that helped their walking (e.g., breathing regulation and awareness, body awareness, mind-body techniques, pacing), described walking as enjoyable, and identified internal reasons for walking (e.g., to feel good). They also reported several physical and mental health benefits of the intervention. Some participants reported limited influence of the intervention on walking or health. Many participants continued to use the strategies they learned in the first half of the intervention at 12-months.</p><p><strong>Conclusions: </strong>The mind-body content of Mindful Steps appeared to positively influence walking behaviors. Participants' experiences with the intervention helped to identify areas for future intervention refinement. Future quantitative work is needed to corroborate these qualitative findings and assess the efficacy of the intervention on long-term physical activity engagement.</p><p><strong>Trial registration: </strong>This trial is registered in Clinical Trials.gov, ID number NCT01551953.</p>","PeriodicalId":73159,"journal":{"name":"Global advances in integrative medicine and health","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693791/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138483577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nutrition and Emotional Health Education: The Use of Emotional Intelligence and a Plant-Based Diet to Reduce Cardiometabolic Risk. 营养和情绪健康教育:利用情商和植物性饮食来降低心脏代谢风险。
Pub Date : 2023-11-17 eCollection Date: 2023-01-01 DOI: 10.1177/27536130231215014
Abd Moain Abu Dabrh, Claire B Haga, Jarik Conrad, Adam I Perlman, Megan A Allyse, Monica L Albertie, Maia Martinez-Heath, Colleen T Ball, Floyd B Willis

Background: For individuals living with chronic conditions like diabetes mellitus and obesity, there is a need for sustainable behavioral strategies and physiologic tools. These tools support identifying and addressing barriers to healthy eating, reducing body mass index (BMI), and building increased physical resilience in real time.

Objective: To evaluate whether a 12-week learning management system designed to combine nutritional intervention with education and coaching on improving emotional intelligence (EI) could alter cardiometabolic outcomes.

Methods: This pre-post prospective study enrolled 37 adult volunteers with BMI greater than 25 to participate in a 12-week learning management system. Primary (BMI, systolic blood pressure, diastolic blood pressure, low-density lipoprotein [LDL], high-density lipoprotein, and fasting glucose levels) and secondary self-reported outcomes were assessed at baseline, 12 weeks, and 6 months after enrollment using Short Form-36, Emotional Quotient Inventory (EQi), and Whole Health Index (WHI). Linear mixed-effects regression models with random effect were used to estimate changes in primary and secondary outcomes. We adjusted for multiple testing using Holm step-down method.

Results: BMI and LDL were the only primary endpoints lower at program completion and 6-month follow-up compared to baseline levels (-1.63 and -17.77 mg/dL, respectively; P < .001). Secondary outcomes showing statistically significant improvement from baseline to 6-month follow-up included energy/fatigue (Short Form-36), self-regard (EQi), decision-making (EQi), impulse control (EQi), stress management (EQi), Whole Brain - Form A (WHI), Whole Food - Form C (WHI), and Whole Body - Form D (WHI).

Conclusion: This study provides preliminary evidence that lifestyle programs combining nutritional interventions and EI can have a significant impact on BMI and LDL. Our study highlights the potential importance of both nutrition and EI in programs targeting diet and lifestyle modification.

背景:对于患有糖尿病和肥胖症等慢性疾病的个体,需要可持续的行为策略和生理工具。这些工具支持识别和解决健康饮食的障碍,降低身体质量指数(BMI),并实时增强身体弹性。目的:评价将营养干预与提高情绪智力(EI)的教育和指导相结合的12周学习管理系统是否能改变心脏代谢结果。方法:本前瞻性研究招募了37名BMI大于25的成年志愿者参加为期12周的学习管理系统。主要(BMI、收缩压、舒张压、低密度脂蛋白(LDL)、高密度脂蛋白和空腹血糖水平)和次要自我报告的结果在入组后基线、12周和6个月使用Short -36、情商量表(EQi)和整体健康指数(WHI)进行评估。采用随机效应的线性混合效应回归模型来估计主要和次要结局的变化。我们使用Holm降压法对多重测试进行了调整。结果:在项目完成和6个月随访时,BMI和LDL是唯一低于基线水平的主要终点(分别为-1.63和-17.77 mg/dL;P < 0.001)。从基线到6个月的随访,显示有统计学显著改善的次要结果包括能量/疲劳(Short Form-36)、自我关注(EQi)、决策(EQi)、冲动控制(EQi)、压力管理(EQi)、全脑- A型(WHI)、全食物- C型(WHI)和全身- D型(WHI)。结论:本研究提供了初步证据,表明生活方式计划结合营养干预和EI可以显著影响BMI和LDL。我们的研究强调了营养和情商在饮食和生活方式改变计划中的潜在重要性。
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引用次数: 0
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Global advances in integrative medicine and health
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