EMDR

EMDR
  • 文章类型: Case Reports
    目的:提出灼口综合征(BMS)的替代治疗方法。
    背景:BMS是一种严重的疾病,对老年人的身体和情绪健康产生负面影响。药物干预在该人群中并不总是合适的,并且可能具有明显的副作用。
    方法:我们介绍了一名86岁的女性,她患有BMS30年,生活质量下降,尤其是睡眠障碍。因为标准的药物未能缓解患者的疼痛,我们提出EMDR作为替代治疗方法.基线测量包括抑郁症状,焦虑症状,白天和夜间疼痛和睡眠质量。为了预测与疼痛相关的焦虑想法,进行了7次45分钟的EMDR课程.
    结果:治疗导致焦虑症状减少(-30%),改善疼痛控制(-10%白天,-60%夜间)和改善睡眠质量(50%)。这种积极的效果持续了4个月,没有观察到严重的负面影响。
    结论:EMDR治疗可以帮助患有BMS的老年人改善疼痛和心理管理。
    OBJECTIVE: To propose an alternative treatment for burning mouth syndrome (BMS).
    BACKGROUND: BMS is a serious condition that negatively affects the physical and emotional health of the elderly. Pharmacological interventions are not always appropriate in this population and may have significant side effects.
    METHODS: We present the case of an 86-year-old woman who has been suffering from BMS for 30 years and has been experiencing impaired quality of life, particularly sleep disturbances. Because standard pharmaceutical medications failed to alleviate the patient\'s pain, we proposed EMDR as an alternative therapeutic approach. Baseline measures included depressive symptoms, anxiety symptoms, daytime and nighttime pain and sleep quality. To anticipate anxious thoughts associated with pain, seven 45-min EMDR sessions were conducted.
    RESULTS: Therapy resulted in reduced anxiety symptoms (-30%), improved pain control (-10% daytime, -60% nighttime) and improved sleep quality (+50%). This positive effect lasted for 4 months, and no serious negative effects were observed.
    CONCLUSIONS: EMDR therapy may help older adults with BMS improve their pain and psychological management.
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  • 文章类型: Journal Article
    创伤后应激障碍(PTSD)是一种以创伤记忆为核心的精神疾病。治疗后的睡眠可以提供独特的时间窗口,以通过巩固治疗修饰的创伤记忆来提高治疗功效。目标记忆再激活(TMR)通过呈现提醒提示(例如,与记忆相关的声音)。这里,我们在PTSD患者中应用了TMR,以在一次眼动脱敏和再处理(EMDR)治疗后增强睡眠期间的治疗记忆.PTSD患者接受慢振荡(SO)相位靶向TMR,使用基于建模的闭环神经刺激(M-CLNS)与EMDR点击作为再激活提示(n=17),或假刺激(n=16)。通过高密度多导睡眠图评估TMR对睡眠的影响。对治疗结果的影响通过主观评估,自主性,和fMRI对目标创伤记忆和整体PTSD症状水平的脚本驱动图像(SDI)的反应。与假刺激相比,TMR导致SO和主轴动态的刺激锁定增加,与TMR组PTSD症状减轻呈正相关。鉴于SO和主轴在内存整合中的作用,这些研究结果表明,TMR可能增强了EMDR治疗记忆的巩固.临床上,TMRvs.假刺激导致SDI期间回避水平的较大降低。TMR不会打扰睡眠或引发噩梦。一起,这些数据首次证明了TMR可能是创伤后应激障碍安全可行的未来治疗增强策略.所需的随访研究可能会在REM睡眠期间实施多夜TMR或TMR,以进一步确定TMR对创伤性记忆的临床效果。
    Post-traumatic stress disorder (PTSD) is a psychiatric disorder with traumatic memories at its core. Post-treatment sleep may offer a unique time window to increase therapeutic efficacy through consolidation of therapeutically modified traumatic memories. Targeted memory reactivation (TMR) enhances memory consolidation by presenting reminder cues (e.g., sounds associated with a memory) during sleep. Here, we applied TMR in PTSD patients to strengthen therapeutic memories during sleep after one treatment session with eye movement desensitization and reprocessing (EMDR). PTSD patients received either slow oscillation (SO) phase-targeted TMR, using modeling-based closed-loop neurostimulation (M-CLNS) with EMDR clicks as a reactivation cue (n = 17), or sham stimulation (n = 16). Effects of TMR on sleep were assessed through high-density polysomnography. Effects on treatment outcome were assessed through subjective, autonomic, and fMRI responses to script-driven imagery (SDI) of the targeted traumatic memory and overall PTSD symptom level. Compared to sham stimulation, TMR led to stimulus-locked increases in SO and spindle dynamics, which correlated positively with PTSD symptom reduction in the TMR group. Given the role of SOs and spindles in memory consolidation, these findings suggest that TMR may have strengthened the consolidation of the EMDR-treatment memory. Clinically, TMR vs. sham stimulation resulted in a larger reduction of avoidance level during SDI. TMR did not disturb sleep or trigger nightmares. Together, these data provide first proof of principle that TMR may be a safe and viable future treatment augmentation strategy for PTSD. The required follow-up studies may implement multi-night TMR or TMR during REM sleep to further establish the clinical effect of TMR for traumatic memories.
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  • 文章类型: Journal Article
    这项研究研究了与标准心理治疗(SP)相比,眼球运动脱敏和再处理(EMDR)疗法在治疗早期儿科肿瘤学患者及其家人的创伤后应激障碍(PTSD)中的疗效癌症治疗。这项研究的次要目的是评估与SP相比,EMDR治疗对创伤后生长的影响是否不同。
    40例患者被随机分配到EMDR或SP组。事件量表-修订(IES-R)和不适温度计(DT)的影响用于评估治疗前(癌症诊断)和治疗后阶段(8个疗程后)的PTSD症状。在治疗后阶段进行创伤后生长量表-PTGI,以评估积极的变化。
    EMDR和SP都能有效减少创伤后应激障碍,但EMDR在降低IES-R评分方面明显比SP更有效,特别是关于侵入性症状分量表。此外,EMDR组的PTGI评分高于标准组.
    EMDR因此代表了儿科心理肿瘤学背景下的一种有希望的治疗方法。
    UNASSIGNED: This study examined the efficacy of eye movement desensitisation and reprocessing (EMDR) therapy compared with standard psychotherapy (SP) in treating post-traumatic stress disorder (PTSD) in paediatric oncology patients and their families in the early stage of cancer treatment. The secondary aim of this study was to assess whether EMDR therapy has a different impact on post-traumatic growth compared to SP.
    UNASSIGNED: Forty patients were randomly assigned to EMDR or SP groups. The Impact of Event Scale - Revised (IES-R) and the Distress Thermometer (DT) were used to assess PTSD symptoms at pre-treatment (at cancer diagnosis) and in the post-treatment stages (after 8 sessions). The Post-traumatic Growth Inventory-PTGI was administered in the post-treatment stage in order to evaluate positive changes.
    UNASSIGNED: Both EMDR and SP are effective in reducing PTSD, but EMDR was significantly more effective than the SP in reducing scores on the IES-R, especially regarding the intrusive symptom subscale. Also, in the EMDR group there were higher scores of PTGI than in the standard group.
    UNASSIGNED: EMDR thus represents a promising treatment in the paediatric psycho-oncology setting.
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  • 文章类型: Journal Article
    有人认为COVID-19大流行是一种潜在的创伤性事件,可能会引起广泛性焦虑和不适,特别是在患有精神疾病的易感人群中。称为眼球运动脱敏和再处理(EMDR)的治疗方法已被证明可以成功地帮助患者处理创伤事件并恢复健康。然而,关于EMDR促进症状恢复的确切过程知之甚少。
    为了解决这些问题,我们进行了一项随机对照试验(ClinicalTrials.govIdentifierNCT06110702),纳入了来自大学医院的107名参与者作为研究样本.对参与者进行随机分配,以将他们分配给实验组和对照组。实验组,但不是对照组,接受了为期8周的EMDR干预.身体感知,厌恶,内疚和羞耻的情绪,以及精神污染和创伤后强迫症状,在EMDR干预前后进行了调查。
    EMDR干预能够改善所研究的所有变量。路径分析表明,身体感知能够预测厌恶和内疚和羞耻的情绪。厌恶能够预测精神污染和强迫症状,而内疚和羞愧能够预测创伤后的症状。
    EMDR是治疗创伤后和强迫性症状的有效疗法,通过促进内/羞耻和厌恶情绪的改善起作用,分别。检查了对临床实践的影响。
    https://www.clinicaltrials.gov,标识符NCT06110702。
    UNASSIGNED: It has been suggested that the COVID-19 pandemic was a potentially traumatic occurrence that may have induced generalized anxiety and discomfort, particularly in susceptible populations like individuals with mental illnesses. The therapeutic approach known as eye movement desensitization and reprocessing (EMDR) has been shown to be successful in helping patients process traumatic events and restore wellbeing. Nevertheless, little is known about the precise processes through which EMDR fosters symptom recovery.
    UNASSIGNED: In order to disentangle these issues, we conducted a randomized controlled trial (ClinicalTrials.gov Identifier NCT06110702) with 107 participants who were selected from university hospitals as a sample of investigation. Random assignments were applied to the participants in order to assign them to the experimental and control groups. The experimental group, but not the control group, underwent an 8-week EMDR intervention. Body perception, disgust, and emotions of guilt and shame, as well as mental contamination and posttraumatic and obsessive-compulsive symptoms, were investigated before and after the EMDR intervention.
    UNASSIGNED: The EMDR intervention was able to improve all of the variables investigated. Path analysis showed that body perception was able to predict both disgust and emotions of guilt and shame. Disgust was able to predict both mental contamination and obsessive-compulsive symptoms, while guilt and shame were able to predict post-traumatic symptoms.
    UNASSIGNED: EMDR is an effective therapy for the treatment of post-traumatic and obsessive symptoms that acts through the promotion of improvement of the emotions of guilt/shame and disgust, respectively. Implications for clinical practice are examined.
    UNASSIGNED: https://www.clinicaltrials.gov, identifier NCT06110702.
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  • 文章类型: Journal Article
    政策制定者,健康保险公司,在选择可能的治疗替代方案时,医疗保健提供者对成本效益分析(CEA)越来越感兴趣,近年来,精神卫生保健的费用一直在增加。
    当前的研究比较了分阶段治疗方法的成本效益和成本效用,该方法包括创伤后应激障碍患者的准备稳定阶段和直接创伤集中治疗和童年虐待史。
    根据一项随机对照试验的数据,对121名因童年虐待而患有PTSD的患者进行了成本-效果分析。将基于阶段的治疗(眼动脱敏和再处理[EMDR]治疗,然后进行情感和人际关系调节技能培训[STAIR];n=57)与直接创伤集中治疗(仅EMDR治疗;n=64)进行了比较。成本-效果的主要结果是缓解PTSD的患者比例。质量调整生命年(QALY)用作成本效用分析的主要结果指标。
    尽管成本效益分析的结果在两组之间没有统计学上的显着差异,每位患者的平均社会成本在STAIR-EMDR和EMDR治疗组之间存在显着差异(19.599欧元与13.501欧元;M成本差异=6.098欧元,CI(95%)=[117欧元;12.644欧元])。
    与仅EMDR治疗相比,STAIR-EMDR不具成本效益。由于以创伤为中心的治疗耗时较少,非创伤集中的相位,由于儿童不良事件,治疗似乎不是治疗PTSD的可行替代方案.临床试验注册:https://onderzoekmetmensen。nl/nl/试用版/22074,标识符NL5836。
    UNASSIGNED: Policymakers, health insurers, and health care providers are becoming increasingly interested in cost-effectiveness analyses (CEA\'s) when choosing between possible treatment alternatives, as costs for mental health care have been increasing in recent years.
    UNASSIGNED: The current study compared the cost-effectiveness and cost-utility of a phased-based treatment approach that included a preparatory stabilization phase with direct trauma-focused treatment in patients with PTSD and a history of childhood abuse.
    UNASSIGNED: A cost-effectiveness analysis was conducted based on data from a randomized controlled trial of 121 patients with PTSD due to childhood abuse. A phase-based treatment (Eye Movement Desensitization and Reprocessing [EMDR] therapy preceded by Skills Training in Affect and Interpersonal Regulation [STAIR]; n = 57) was compared with a direct trauma-focused treatment (EMDR therapy only; n = 64). The primary outcome of cost-effectiveness was the proportion of patients with remitted PTSD. Quality-adjusted life years (QALY) were used as the primary outcome measure for cost-utility analysis.
    UNASSIGNED: Although the results of the cost-effectiveness analyses yielded no statistically significant differences between the two groups, the mean societal costs per patient differed significantly between the STAIR-EMDR and EMDR therapy groups (€19.599 vs. €13.501; M cost differences = €6.098, CI (95%) = [€117; €12.644]).
    UNASSIGNED: STAIR-EMDR is not cost-effective compared with EMDR-only therapy. Since trauma-focused treatment is less time-consuming, non-trauma-focused phase-based, treatment does not seem to be a viable alternative for the treatment of PTSD due to adverse childhood events.Clinical trial registration: https://onderzoekmetmensen.nl/nl/trial/22074, identifier NL5836.
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  • 文章类型: Journal Article
    双侧刺激是眼动脱敏和后处理疗法的核心要素,用于治疗创伤后应激障碍(PTSD)的心理治疗干预。有希望的先前发现表明,在健康个体中,双侧刺激可测量的生理效应,但是在PTSD患者中重复这些发现的研究很少。
    23名PTSD患者和30名健康对照者面对情感标准脚本(愉快,中性,不愉快),同时施加双侧触觉刺激。单外侧和无刺激作为对照条件。噪声引起的惊吓反射反应(效价测量)和皮肤电反应(唤醒测量)用于生理反应,而自我评估人体模型的效价和唤醒量表用于主观反应。
    两组在双侧刺激下表现出令人不快的脚本的主观痛苦减少和积极脚本的主观注意力增加。在健康的个体中,这也是为了生理测量,发现在没有情感刺激的情况下,双侧刺激具有一般的减轻惊吓的作用。在PTSD患者中,然而,效果在主观层面上受到限制,并且没有观察到伴随的生理效应。
    研究结果表明,将BLS在健康个体中的作用推广到PTSD患者可能是有问题的。本文报道的组差异可以通过情感处理和认知处理风格中的PTSD特异性来解释。
    UNASSIGNED: Bilateral stimulation is a core element of Eye Movement Desensitization and Reprocessing Therapy, a psychotherapeutic intervention for the treatment of Posttraumatic Stress Disorder (PTSD). Promising previous findings showed measurable physiological effects of bilateral stimulation in healthy individuals, but studies that replicated these findings in PTSD patients are sparse.
    UNASSIGNED: 23 patients with PTSD and 30 healthy controls were confronted with affective standard scripts (pleasant, neutral, unpleasant) while bilateral tactile stimulation was applied. Monolateral and no stimulation served as control conditions. Noise-induced startle reflex response (valence measure) and galvanic skin response (arousal measure) were used for physiological responses and the valence and arousal scale of the Self-Assessment-Manikin for subjective responses.
    UNASSIGNED: Both groups showed a subjective distress reduction for unpleasant scripts and a subjective attention increase for positive scripts under bilateral stimulation. In healthy individuals, this was also for physiological measures, and a general startle-reducing effect of bilateral stimulation in the absence of affective stimuli was found. In PTSD patients, however, the effects were restricted on the subjective level, and no concomitant physiological effects were observed.
    UNASSIGNED: The findings indicate, that generalizing the effects of BLS in healthy individuals to PTSD patients may be problematic. The herein-reported group differences can be explained by PTSD-specific peculiarities in emotion processing and cognitive processing style.
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  • 文章类型: Journal Article
    叙利亚冲突自2011年以来一直持续。鉴于临床医生的可用性有限,迫切需要实用且可扩展的解决方案来满足对创伤后应激障碍的专业心理支持需求的增加。对具有心理健康背景的被迫流离失所的叙利亚人进行培训,以远程提供专门的干预措施,可以增加基于证据的心理支持。对于被迫流离失所的叙利亚妇女治疗师提供的在线治疗对被迫流离失所的叙利亚妇女的有效性知之甚少。
    为了进行循证创伤治疗,眼动脱敏和再处理(EMDR)由训练有素的被迫流离失所的叙利亚妇女治疗师在线进行,以治疗需要治疗创伤后应激障碍(PTSD)的被迫流离失所的叙利亚妇女。
    83名被迫流离失所的叙利亚妇女,住在图尔基耶或叙利亚境内,有可诊断的创伤后应激障碍,在3个月的时间内提供了多达12次在线EMDR。这是由接受EMDR培训的被迫流离失所的叙利亚妇女治疗师提供的。收集了数据,使用阿拉伯语版本,使用事件影响量表修订后的创伤后应激障碍症状,使用患者健康问卷-9的抑郁症状和使用基线时的广泛性焦虑症评估-7的焦虑症状,中点,治疗结束.
    PTSD得分,在治疗过程中,抑郁评分和焦虑评分均显着降低,中点得分低于基线,治疗结束时得分低于中点。只有一名参与者(1%)超过了创伤后应激障碍的临界点,治疗结束时,13例(16%)超过焦虑和抑郁的临界点.
    在这项初步研究中,多达12次在线EMDR与PTSD的减少有关,受叙利亚冲突影响的叙利亚妇女的焦虑和抑郁症状。培训被迫流离失所的叙利亚精神卫生专业人员提供在线治疗的成本相对较低,可扩展,可持续的解决方案,以确保受冲突影响的人能够获得专门的支持。需要使用对照组进行进一步的研究,以确认观察到的效果是由于EMDR治疗,治疗后随访的研究也是如此,以确定获益是否得到维持。
    UNASSIGNED: The Syrian conflict has been ongoing since 2011. Practical and scalable solutions are urgently needed to meet an increase in need for specialised psychological support for post-traumatic stress disorder given limited availability of clinicians. Training forcibly displaced Syrians with a mental health background to remotely deliver specialised interventions increases the availability of evidence based psychological support. Little is known about the effectiveness of online therapy for forcibly displaced Syrian women provided by forcibly displaced Syrian women therapists.
    UNASSIGNED: To pilot an evidence-based trauma therapy, Eye Movement Desensitisation and Reprocessing (EMDR), carried out online by trained forcibly displaced Syrian women therapists for forcibly displaced Syrian women who require treatment for post-traumatic stress disorder (PTSD).
    UNASSIGNED: 83 forcibly displaced Syrian women, living in Türkiye or inside Syria, with diagnosable PTSD, were offered up to 12 sessions of online EMDR over a period of 3 months. This was delivered by forcibly displaced Syrian women therapists who were trained in EMDR. Data were gathered, using Arabic versions, on PTSD symptoms using the Impact of Events Scale Revised, depression symptoms using the Patient Health Questionnaire-9 and anxiety symptoms using the Generalised Anxiety Disorder Assessment-7 at baseline, mid-point, and end of therapy.
    UNASSIGNED: PTSD scores, depression scores and anxiety scores all significantly reduced over the course of treatment, with lower scores at midpoint than baseline and lower scores at end of treatment than at midpoint. Only one participant (1%) exceeded the cutoff point for PTSD, and 13 (16%) exceeded the cutoff points for anxiety and depression at the end of treatment.
    UNASSIGNED: In this pilot study up to 12 sessions of online EMDR were associated with reductions in PTSD, anxiety and depression symptoms in Syrian women affected by the Syrian conflict. The training of forcibly displaced Syrian mental health professionals to deliver online therapy is a relatively low cost, scalable, sustainable solution to ensure that those who are affected by the conflict can access specialised support. Further research is needed using a control group to confirm that the observed effects are due to EMDR treatment, as is research with post-treatment follow-up to ascertain that benefits are maintained.
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  • 文章类型: Journal Article
    童年时期的性虐待仍然是一种痛苦的社会现实,需要机构和医疗保健专业人员的回应,以预防和解决其对受害者的严重长期后果。这项研究实施了一项干预措施,包括世界卫生组织推荐的两种心理治疗方法和国际临床指南,medium-,和长期创伤后症状学:创伤集中的认知行为治疗(TF-CBT)和眼动脱敏和再处理(EMDR)。两种方法都改编自组格式,以便通过Zoom在小型在线组中实现。
    通过一项比较EMDR心理治疗和创伤聚焦认知行为治疗的随机临床试验,在19名儿童性虐待受害者的样本中评估了两种治疗方法对创伤改善的影响。基线期。使用适合样品的统计学进行内部和内部比较。
    两种治疗方法都显着降低了各种评估变量的症状学,表明它们在改善这些人的生活质量方面的功效。CBT-FT治疗后,患者表现出增强的情绪调节,减少重新体验,和回避。EMDR组,利用G-TEP组协议,显著改善解离,以及其他关键的临床变量和对生活质量的看法。
    尽管由于样本的大小和缺乏长期随访,必须考虑到这项研究的局限性,结果与现有的科学文献一致,强调以创伤为中心的心理治疗的好处。在线小组格式似乎有望增强这些妇女的心理治疗的可及性。此外,每种治疗的不同结局支持了最近的研究,该研究主张将这两种方法纳入创伤相关症状的个体.
    该研究已获得瓦伦西亚国际大学(VIU)伦理委员会的批准(瓦伦西亚,西班牙)(参考文献。CEID2021_07)。结果将提交给同行评审的期刊发表,并分发给科学界。
    https://clinicaltrials.gov/ct2/show/NCT04813224,标识符NCT04813224。
    UNASSIGNED: Childhood sexual abuse persists as a painful societal reality, necessitating responses from institutions and healthcare professionals to prevent and address its severe long-term consequences in victims. This study implements an intervention comprising two psychotherapeutic approaches recommended by the WHO and international clinical guidelines for addressing short-, medium-, and long-term posttraumatic symptomatology: Trauma-Focused Cognitive Behavioral Therapy (TF-CBT) and Eye Movement Desensitization and Reprocessing (EMDR). Both approaches are adapted from group formats for implementation in small online groups via Zoom.
    UNASSIGNED: The impact of both therapeutic approaches on trauma improvement was assessed in a sample of 19 women who were victims of childhood sexual abuse through a Randomized Clinical Trial comparing EMDR Psychotherapy and Trauma-Focused Cognitive Behavioral Therapy after a baseline period. Intra and inter comparison were made using statistics appropriate to the sample.
    UNASSIGNED: Both therapeutic approaches significantly reduced symptomatology across various evaluated variables, suggesting their efficacy in improving the quality of life for these individuals. Following CBT-FT treatment, patients exhibited enhanced emotional regulation, reduced reexperiencing, and avoidance. The EMDR group, utilizing the G-TEP group protocol, significantly improved dissociation, along with other crucial clinical variables and the perception of quality of life.
    UNASSIGNED: Although the limitations of this study must be taken into account due to the size of the sample and the lack of long-term follow-up, the results align with existing scientific literature, underscoring the benefits of trauma-focused psychological treatments. The online group format appears promising for enhancing the accessibility of psychological treatment for these women. Furthermore, the differential outcomes of each treatment support recent research advocating for the inclusion of both approaches for individuals with trauma-related symptomatology.
    UNASSIGNED: The study has been approved by the Ethics Committee of the Valencian International University (VIU) (Valencia, Spain) (Ref. CEID2021_07). The results will be submitted for publication in peer-reviewed journals and disseminated to the scientific community.
    UNASSIGNED: https://clinicaltrials.gov/ct2/show/NCT04813224, identifier NCT04813224.
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  • 文章类型: Journal Article
    强化住院治疗计划在创伤后应激障碍(PTSD)的治疗中显示出良好的效果。患者如何体验这种治疗方案,以及由于治疗而经历的变化,然而,只有很少通过定性研究进行探索。
    本研究旨在探索在强化住院创伤治疗计划中参与者的生活体验。我们的研究问题如下:患者如何经历以创伤为中心的强化治疗?他们如何经历与参与治疗计划相关的可能变化?
    6例诊断为PTSD并伴有明显合并症的患者,最近参加了为期2周(4+4天)的强化住院创伤治疗计划,眼球运动脱敏和后处理(EMDR),和治疗师轮换(TR),接受了半结构化定性访谈。使用主题分析方法分析了成绩单。
    我们的分析得出了五个主要主题:(1)需要感到安全;(2)许多不同的治疗方法的好处;(3)治疗要素的可变经验;(4)强度;(5)经历的变化。我们的结果表明,在治疗计划的框架内感到安全可以促进治疗过程。许多不同的治疗遭遇,通过TR和病房工作人员,促成了经历的变革。所有参与者都将强度描述为促进创伤处理。然而,大多数参与者还描述了经常感到不知所措,无法从治疗计划的所有要素中受益。
    我们的研究结果表明,参与者体验整体治疗方案是有益的,并有助于经历变化。参与者将该计划的强度描述为令人筋疲力尽,但必要的。大多数人都这样做了,然而,报告过于不堪重负,无法从该计划的要素中受益。因此,我们的结果促使我们质疑最佳强度水平。
    ClinicalTrials.gov标识符:NCT05342480。注册日期:2022-04-22。
    UNASSIGNED: Intensive inpatient treatment programs have shown robust results in the treatment of post-traumatic stress disorder (PTSD). How patients experience this treatment program and what changes they experience as a result of the treatment have, however, only scarcely been explored through qualitative studies.
    UNASSIGNED: This study aimed to explore the lived experience of participants in an intensive inpatient trauma treatment program. Our research questions were as follows: how do patients experience intensive trauma-focused treatment? How do they experience possible changes related to participating in the treatment program?
    UNASSIGNED: Six patients diagnosed with PTSD with significant comorbidities, who recently participated in an intensive 2-week (4 + 4 days) inpatient trauma treatment program with prolonged exposure (PE), eye movement desensitization and reprocessing (EMDR), and therapist rotation (TR), were interviewed with a semi-structured qualitative interview. Transcripts were analyzed using a thematic analysis approach.
    UNASSIGNED: Our analysis resulted in five main themes: (1) the need to feel safe; (2) the benefits of many and different therapeutic encounters; (3) variable experience with elements of treatment; (4) intensity; and (5) experienced change. Our results suggest that feeling safe within the framework of the treatment program facilitated the treatment process. Many and different therapeutic encounters, both through TR and with ward staff, contributed to experienced change. All participants described the intensity as facilitative to trauma processing. However, most participants also describe often feeling too overwhelmed to benefit from all elements of the treatment program.
    UNASSIGNED: Our findings suggest that participants experience the overall treatment program as beneficial and contributing to experienced change. Participants described the intensity of the program as exhausting, but necessary. Most did, however, report at times of being too overwhelmed to benefit from elements of the program. Consequently, our results prompt us to question the optimal level of intensity.
    UNASSIGNED: ClinicalTrials.gov identifier: NCT05342480. Date of registration: 2022-04-22.
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  • 文章类型: Journal Article
    除了药物治疗,建议采用心理治疗方法治疗纤维肌痛。有人建议,眼球运动脱敏和后处理(EMDR)治疗可能是有效的。本研究旨在探讨EMDR治疗对纤维肌痛症状的影响,抑郁症,睡眠质量,通过随机对照研究(RCT),纤维肌痛患者的创伤应激。
    本研究的样本包括79名诊断为纤维肌痛的个体。参与者被随机分为两组:“照常治疗”(TAU)组和TAUEMDR组。在研究之前和六个不同的时间点(在开始研究之前,在5号结束的时候,第十,第十五届会议,一个月后,3个月后),参与者完成了评估,包括纤维肌痛影响问卷(FIQ),视觉模拟量表(VAS),纤维肌痛ACR2010诊断标准[广泛疼痛指数(WPI)和症状严重程度量表(SSS)],贝克抑郁量表(BDI),匹兹堡睡眠质量指数(PSQI)和创伤症状清单-40(TSC-40)。
    研究组和实验组之间的社会人口统计学变量没有差异。方差分析显示,对VAS有统计学意义的群体效应(p=0.019),WPI(p=0.018),BDI(p=0.019),和TSC-40(p=0.21)。在应用Bonferroni校正后,发现EMDR对VAS有效,WPI,SSS,BDI,PSQI,和TSC-40(p<0.05)。
    当前研究的结果表明,EMDR疗法是纤维肌痛的可行替代疗法。我们相信这些发现提供了有力的证据支持EMDR疗法治疗纤维肌痛的疗效。特别是在随机对照试验(RCT)的背景下。应用EMDR疗法治疗纤维肌痛患者可能是有益的。
    ClinicalTrials.gov,标识符NCT06265194。
    UNASSIGNED: In addition to pharmacological treatment, psychotherapeutic approaches are recommended for the treatment of fibromyalgia. There is a suggestion that eye movement desensitization and reprocessing (EMDR) therapy may be effective. This study aimed to investigate the impact of EMDR therapy on fibromyalgia symptoms, depression, sleep quality, and traumatic stress in fibromyalgia patients through a randomized controlled study (RCT).
    UNASSIGNED: The sample for this study comprised 79 individuals diagnosed with fibromyalgia. Participants were randomly assigned to two groups: the \"Treatment as Usual\" (TAU) group and the TAU + EMDR group. Prior to the study and at six different time points (before starting the study, at the end of the 5th, 10th, and 15th sessions, 1 month later, and 3 months later), participants completed assessments, including the Fibromyalgia Impact Questionnaire (FIQ), Visual Analog Scale (VAS), Fibromyalgia ACR 2010 Diagnostic Criteria [Widespread Pain Index (WPI) and Symptom Severity Scale (SSS)], Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), and Trauma Symptom Checklist-40 (TSC-40).
    UNASSIGNED: There were no differences in the sociodemographic variables between the study and experimental groups. Analysis of variance revealed a statistically significant group effect on VAS (p = 0.019), WPI (p = 0.018), BDI (p = 0.019), and TSC-40 (p = 0.21). After applying Bonferroni correction, EMDR was found to be effective for VAS, WPI, SSS, BDI, PSQI, and TSC-40 (p <0.05).
    UNASSIGNED: The results of the current study suggest that EMDR therapy is a viable alternative treatment for fibromyalgia. We believe these findings offer robust evidence supporting the efficacy of EMDR therapy in treating fibromyalgia, particularly in the context of a randomized controlled trial (RCT). The application of EMDR therapy for the treatment of patients with fibromyalgia is likely to be beneficial.
    UNASSIGNED: ClinicalTrials.gov, identifier NCT06265194.
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