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Trajectory of severe COVID anxiety and predictors for recovery in an 18-month UK cohort. 英国18个月队列中严重COVID焦虑的轨迹和康复预测因素
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-03 DOI: 10.1192/bjo.2025.10884
Jacob D King, Aisling McQuaid, Kirsten Barnicot, Paul Bassett, Verity C Leeson, Martina Di Simplicio, Peter Tyrer, Helen Tyrer, Richard G Watt, Mike J Crawford

Background: People with severe COVID anxiety have significant fears of contagion, physiological symptoms of anxiety in response to a COVID stimulus and employ often disproportionate safety behaviours at the expense of other life priorities.

Aims: To characterise the long-term trajectory of severe COVID anxiety, and the factors that influence recovery.

Method: This prospective cohort study followed 285 people with severe COVID anxiety in the UK over 18 months. A nested randomised feasibility trial tested an online cognitive-behavioural therapy (CBT)-based intervention (no. ISRCTN14973494). Descriptive statistics and linear regression models identified factors associated with change in COVID anxiety over 18 months.

Results: Most participants experienced major reductions in COVID anxiety over time (69.8% relative cohort mean decrease, P < 0.001), but a quarter of people (23.7%, 95% CI: 17.8-30.1) continued to worry about COVID every day, and for 13% symptoms remained severe even after the ending of all public health restrictions. Increasing age, being from a minority ethnic background that confers greater risk from COVID-19, and the persistence of high levels of health anxiety and depressive symptoms, predicted slower improvements in severe COVID anxiety after adjusting for other clinical and demographic factors. Neither a trial CBT-based intervention, nor contextual factors including daily case rates, vaccination status or having contracted COVID-19, appeared to affect the trajectory of severe COVID anxiety.

Conclusions: For most people severe COVID anxiety improves significantly with time. However, interventions treating depression and health anxiety, and targeting older people and those from greater-risk minority backgrounds, warrant further investigation in future pandemics.

背景:患有严重COVID焦虑的人对感染有明显的恐惧,对COVID刺激有焦虑的生理症状,并且往往以牺牲其他生活优先事项为代价采取不成比例的安全行为。目的:描述严重COVID焦虑的长期轨迹,以及影响康复的因素。方法:这项前瞻性队列研究对英国285名严重COVID焦虑患者进行了为期18个月的随访。一项嵌套随机可行性试验测试了一种基于认知行为疗法(CBT)的在线干预(no。ISRCTN14973494)。描述性统计和线性回归模型确定了与18个月内COVID焦虑变化相关的因素。结果:随着时间的推移,大多数参与者的COVID焦虑显著减少(相对队列平均减少69.8%,P < 0.001),但四分之一的人(23.7%,95% CI: 17.8-30.1)继续每天担心COVID, 13%的人即使在所有公共卫生限制结束后症状仍然严重。随着年龄的增长,来自少数民族背景的人患COVID-19的风险更大,以及持续存在高水平的健康焦虑和抑郁症状,在调整了其他临床和人口因素后,预测严重的COVID-19焦虑的改善速度较慢。基于cbt的干预试验,以及包括每日病例率、疫苗接种状况或感染COVID-19在内的背景因素,似乎都没有影响严重COVID-19焦虑的轨迹。结论:对于大多数人来说,严重的COVID焦虑会随着时间的推移而显著改善。然而,治疗抑郁和健康焦虑的干预措施,以及针对老年人和高风险少数民族背景的干预措施,值得在未来的大流行中进一步调查。
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引用次数: 0
Reporting of side-effects in clinical trials of psilocybin-assisted psychotherapy for psychiatric conditions: systematic review. 报告裸盖菇素辅助心理治疗精神疾病临床试验中的副作用:系统评价。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-03 DOI: 10.1192/bjo.2025.10847
Jonathon Marinis, Sarah T Clarke, Alexandre A Guerin, Adam J Guastella, Gillinder Bedi

Background: Psilocybin-assisted psychotherapy (PAP) has gained attention as a promising intervention for conditions including depression, anxiety and post-traumatic stress disorder, but understanding of its side-effects is limited. This review evaluates the quality of side-effects reporting in PAP trials, to guide treatment, policy and research.

Aims: To assess side-effects reporting quality in PAP trials for psychiatric conditions, comparing published articles and ClinicalTrials.gov records.

Method: A PROSPERO-registered review (no. CRD42023458960) included English-language PAP trials (2005-2024) identified via Embase, CENTRAL, PubMed and reference searches. Reporting quality was assessed using the CONSORT Harms extension, categorised as either high (17-21), moderate (12-16), low (7-11) or very low (0-6). Randomised controlled trials underwent risk of bias analysis, and descriptive statistics compared side-effects across sources.

Results: Twenty-four trials were included. Reporting quality was high in six studies, moderate in four, low in nine and very low in five. All randomised controlled trials (n = 9) showed high risk of bias for side-effects outcomes. Variability in reporting hindered comparisons between articles and ClinicalTrials.gov, underscoring the need for standardisation. Overall, there was no evidence of systematic underreporting of side-effects in published articles compared with trial registers.

Conclusions: Side-effects reporting in PAP trials is inconsistent but is improving over time. Existing evidence has a high risk of bias. Future trials should align with best-practice guidelines for side-effects reporting. Discussions with patients should prioritise findings from high-quality studies and emphasise the current uncertainty regarding PAP side-effects.

背景:裸盖菇素辅助心理治疗(PAP)作为一种有希望的治疗抑郁症、焦虑症和创伤后应激障碍的方法而受到关注,但对其副作用的了解有限。本综述评价PAP试验中副作用报告的质量,以指导治疗、政策和研究。目的:通过比较已发表的文章和ClinicalTrials.gov的记录,评估PAP治疗精神疾病试验的副作用报告质量。方法:普洛斯普洛斯注册评审(no。CRD42023458960)包括通过Embase、CENTRAL、PubMed和参考文献检索确定的英文PAP试验(2005-2024)。使用CONSORT危害扩展评估报告质量,分为高(17-21)、中(12-16)、低(7-11)或极低(0-6)。随机对照试验进行了风险偏倚分析,描述性统计比较了不同来源的副作用。结果:共纳入24项试验。报告质量高的研究有6项,中等的有4项,低的有9项,极低的有5项。所有随机对照试验(n = 9)均显示副作用结果的高偏倚风险。报告的可变性阻碍了文章与ClinicalTrials.gov之间的比较,强调了标准化的必要性。总的来说,与试验登记相比,没有证据表明发表的文章中系统性地少报了副作用。结论:PAP试验的副作用报告不一致,但随着时间的推移正在改善。现有证据有很高的偏倚风险。未来的试验应与副作用报告的最佳实践指南保持一致。与患者的讨论应优先考虑高质量研究的结果,并强调目前PAP副作用的不确定性。
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引用次数: 0
Comparison of suicide rates in the USA and Australia between 1921 and 2020: major shifts in youth and elderly suicide rates over a century. 1921年至2020年间美国和澳大利亚自杀率的比较:一个世纪以来青年和老年人自杀率的重大变化。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-30 DOI: 10.1192/bjo.2025.10863
Sydney Z Ma, Shahid Ullah, Stephen Allison, Stephen R Kisely, Jeffrey C L Looi, Tarun Bastiampillai

Background: Trends in the US and Australian suicide mortality have shifted over the last 100 years, with notable differences between age groups and genders.

Aims: This study compared overall and gender- and age-specific suicide rates from 1921 to 2020 in the USA and Australia to determine long-term variation for each country.

Method: Suicide data (1921-2020, inclusive) were obtained from the US Centers for Disease Control and Prevention and the Australian Institute of Health and Welfare. Poisson regression was used to assess whether suicide rates between groups were significantly different.

Results: Overall suicide rates were higher in the USA compared to Australia, from 1921 to the 1940s, but were similar from the 1950s onwards. While male suicide rates fluctuated, female suicide rates were relatively stable (except for Australian women in the 1960s). In the USA and Australia, suicide rates for young males have significantly increased since the 1950s, while they have decreased for the older male population since the 1940s.

Conclusions: While overall national suicide rates were relatively stable over 100 years apart from during war and economic depression, male suicide rates in the USA and Australia experienced significant age-related changes over the century. These include major declines in males aged over 65 years but also an increase in suicides for those aged between 15 and 44. Suicide rates across age groups have therefore converged, regressing towards the mean for all age groups combined.

背景:在过去的100年里,美国和澳大利亚的自杀死亡率趋势发生了变化,在年龄组和性别之间存在显著差异。目的:本研究比较了美国和澳大利亚从1921年到2020年的总体自杀率和特定性别和年龄的自杀率,以确定每个国家的长期变化。方法:自杀数据(1921-2020年,包括)来自美国疾病控制与预防中心和澳大利亚健康与福利研究所。用泊松回归评估组间自杀率是否有显著差异。结果:从1921年到20世纪40年代,美国的总体自杀率高于澳大利亚,但从20世纪50年代起,两者相似。男性自杀率波动,而女性自杀率相对稳定(20世纪60年代的澳大利亚女性除外)。在美国和澳大利亚,自20世纪50年代以来,年轻男性的自杀率显著上升,而自20世纪40年代以来,老年男性的自杀率有所下降。结论:除了战争和经济萧条期间,美国和澳大利亚的男性自杀率在过去的100年里相对稳定,但在过去的一个世纪里,男性自杀率经历了与年龄相关的重大变化。其中包括65岁以上男性自杀率大幅下降,但15岁至44岁男性自杀率也有所上升。因此,各年龄组的自杀率趋于一致,向所有年龄组的平均值回归。
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引用次数: 0
Psychometric validation of the Italian Gender Preoccupation and Stability Questionnaire in a gender-diverse clinical sample. 意大利性别关注和稳定性问卷在性别多样化临床样本中的心理测量验证。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-28 DOI: 10.1192/bjo.2025.10879
Paolo Meneguzzo, David Dal Brun, Alberto Scala, Marina Bonato, Andrea Garolla, Marina Miscioscia, Elena Tenconi, Angela Favaro

Background: Understanding gender identity in transgender and gender-diverse (TGD) individuals is crucial for effective care. The Gender Preoccupation and Stability Questionnaire (GPSQ) measures the preoccupation and stability of gender identity, but no Italian validation is available.

Aims: This study aimed to translate, culturally adapt and validate the Italian version of the GPSQ in a clinical sample of TGD adults.

Method: The GPSQ was translated with a forward-backward method and completed by 151 TGD adults at a gender clinic. Participants also filled out the Symptom Checklist-58 and Body Uneasiness Test. We assessed structural validity (EFA), internal consistency, test-retest reliability, and examined known-groups and predictive validity.

Results: The EFA supported a four-factor structure - Gender Identity Instability, Cognitive-Affective Salience, Preoccupation, and Distress/Intervention-Oriented Reflection - with good fit (root mean square error of approximation 0.06; Comparative Fit Index 0.95; Tucker-Lewis Index 0.93; standard root mean square residual 0.04). The GPSQ showed solid internal consistency (α = 0.78; ω = 0.73) and excellent test-retest reliability (r = 0.98; intraclass correlation coefficient 0.98). Higher scores correlated with psychological distress (r = 0.55, p < 0.001) and body image concerns (r = 0.48, p < 0.001). Preoccupation was most linked to obsessive-compulsive symptoms, and Cognitive-Affective Salience to body image concerns. Participants not on hormones scored higher (p = 0.010, Cohen's d = 0.36).

Conclusions: The Italian GPSQ is a reliable and valid tool to assess gender-related preoccupation and identity instability in TGD individuals. Its multidimensional structure makes it useful in both clinical practice and research in the Italian context.

背景:了解跨性别和性别多样性(TGD)个体的性别认同对有效护理至关重要。性别关注和稳定性问卷(GPSQ)测量性别认同的关注和稳定性,但没有意大利验证可用。目的:本研究旨在对TGD成人临床样本中意大利语版GPSQ进行翻译、文化适应和验证。方法:在某性别诊所对151名TGD成人进行GPSQ正反译法翻译。参与者还填写了症状表-58和身体不适测试。我们评估了结构效度(EFA)、内部一致性、重测信度,并检查了已知组和预测效度。结果:EFA支持四因素结构——性别认同不稳定性、认知-情感显著性、关注和困扰/干预导向反思——拟合良好(均方根误差近似0.06;比较拟合指数0.95;Tucker-Lewis指数0.93;标准均方根残差0.04)。GPSQ具有良好的内部一致性(α = 0.78, ω = 0.73)和良好的重测信度(r = 0.98,类内相关系数0.98)。较高的分数与心理困扰(r = 0.55, p < 0.001)和身体形象担忧(r = 0.48, p < 0.001)相关。专注与强迫症症状最相关,而认知情感突出与身体形象担忧最相关。未使用激素的参与者得分更高(p = 0.010, Cohen’s d = 0.36)。结论:意大利GPSQ是评估TGD个体性别相关关注和身份不稳定性的可靠有效工具。它的多维结构使其在意大利的临床实践和研究中都很有用。
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引用次数: 0
Reminiscence and grief resolution through online journalling: mixed-methods analysis of the Living Memory Home bereavement cohort. 通过在线日志的回忆和悲伤解决:生活记忆家庭丧亲队列的混合方法分析。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-28 DOI: 10.1192/bjo.2025.10882
Courtney E Lee, Holly G Prigerson, Francesca Falzarano, Madeline Rogers, Francesco Osso, Sosi Korian, Charlotte LaPlante, Madison Pavao, Jin Pyon, Wan Jou She, Hillary Winoker, Alexandra Pitman, Kailey Roberts, Paul K Maciejewski

Background: Prolonged grief disorder (PGD) is a chronic, impairing state of intense grief that is responsive to specialised intervention. Online journalling has the potential to reduce PGD symptoms.

Aims: To assess whether reminiscence via online journalling facilitates bereavement adjustment - specifically, to identify key themes in online grief journals and examine associations between types of reminiscence and changes in PGD symptom severity.

Method: A cohort of 96 bereaved adults completed 7 days of online journalling on the Living Memory Home (LMH) bereavement website. Participants were recruited from clinics, bereavement support groups and a National Institutes of Health-funded, web-based platform. The Prolonged Grief Disorder-Revised scale (PG-13-R) was administered at baseline and at 1-week and 1-month follow-up.

Results: Descriptive analysis revealed a reduction in PG-13-R scores from baseline to 1-week follow-up (mean difference -3.7, 95% CI: -4.9, -2.5, P < 0.001) and 1-month follow-up (mean difference -5.0, 95% CI: -6.4, -3.7. P < 0.001). Mixed-methods analysis revealed significant negative associations between reflection on negative traits of the deceased and PG-13-R score at all three time points, and between reflection on past experiences with the deceased and PG-13-R score at baseline. Expression of regret and guilt was significantly associated with reduction in PG-13-R scores from 1-week to 1-month follow-up.

Conclusions: Engagement in the LMH website demonstrated significant declines in PGD symptom severity after 1 week of online journalling and at 1-month follow-up. Guided reflection on memories of the deceased, and even on negative or emotionally challenging memories, shows potential for reducing symptoms of PGD.

背景:延长悲伤障碍(PGD)是一种慢性的,损害状态的强烈悲伤,是响应专门的干预。在线日志有可能减少PGD症状。目的:评估通过在线日记进行的回忆是否有助于丧亲调整——具体而言,确定在线悲伤日记中的关键主题,并检查回忆类型与PGD症状严重程度变化之间的关联。方法:一组96名丧亲成人在“生活记忆之家”丧亲网站上完成了7天的在线日志。参与者是从诊所、丧亲支持团体和美国国立卫生研究院资助的网络平台招募的。延长悲伤障碍修正量表(PG-13-R)在基线和1周和1个月的随访中进行。结果:描述性分析显示PG-13-R评分从基线到随访1周(平均差值-3.7,95% CI: -4.9, -2.5, P < 0.001)和随访1个月(平均差值-5.0,95% CI: -6.4, -3.7)降低。P < 0.001)。混合方法分析显示,在所有三个时间点上,对死者负面特征的反思与PG-13-R评分之间存在显著的负相关,对死者过去经历的反思与基线时的PG-13-R评分之间存在显著的负相关。从1周到1个月的随访中,后悔和内疚的表达与PG-13-R评分的降低显著相关。结论:在1周的在线日志和1个月的随访后,参与LMH网站显示PGD症状严重程度显着下降。引导反思死者的记忆,甚至是消极的或情感上具有挑战性的记忆,显示出减少PGD症状的潜力。
{"title":"Reminiscence and grief resolution through online journalling: mixed-methods analysis of the Living Memory Home bereavement cohort.","authors":"Courtney E Lee, Holly G Prigerson, Francesca Falzarano, Madeline Rogers, Francesco Osso, Sosi Korian, Charlotte LaPlante, Madison Pavao, Jin Pyon, Wan Jou She, Hillary Winoker, Alexandra Pitman, Kailey Roberts, Paul K Maciejewski","doi":"10.1192/bjo.2025.10882","DOIUrl":"10.1192/bjo.2025.10882","url":null,"abstract":"<p><strong>Background: </strong>Prolonged grief disorder (PGD) is a chronic, impairing state of intense grief that is responsive to specialised intervention. Online journalling has the potential to reduce PGD symptoms.</p><p><strong>Aims: </strong>To assess whether reminiscence via online journalling facilitates bereavement adjustment - specifically, to identify key themes in online grief journals and examine associations between types of reminiscence and changes in PGD symptom severity.</p><p><strong>Method: </strong>A cohort of 96 bereaved adults completed 7 days of online journalling on the Living Memory Home (LMH) bereavement website. Participants were recruited from clinics, bereavement support groups and a National Institutes of Health-funded, web-based platform. The Prolonged Grief Disorder-Revised scale (PG-13-R) was administered at baseline and at 1-week and 1-month follow-up.</p><p><strong>Results: </strong>Descriptive analysis revealed a reduction in PG-13-R scores from baseline to 1-week follow-up (mean difference -3.7, 95% CI: -4.9, -2.5, <i>P</i> < 0.001) and 1-month follow-up (mean difference -5.0, 95% CI: -6.4, -3.7. <i>P</i> < 0.001). Mixed-methods analysis revealed significant negative associations between reflection on negative traits of the deceased and PG-13-R score at all three time points, and between reflection on past experiences with the deceased and PG-13-R score at baseline. Expression of regret and guilt was significantly associated with reduction in PG-13-R scores from 1-week to 1-month follow-up.</p><p><strong>Conclusions: </strong>Engagement in the LMH website demonstrated significant declines in PGD symptom severity after 1 week of online journalling and at 1-month follow-up. Guided reflection on memories of the deceased, and even on negative or emotionally challenging memories, shows potential for reducing symptoms of PGD.</p>","PeriodicalId":9038,"journal":{"name":"BJPsych Open","volume":"11 6","pages":"e259"},"PeriodicalIF":3.5,"publicationDate":"2025-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12569618/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145375809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Behaviours that challenge in children with intellectual disability: systematic review and meta-analysis of pharmacological and non-pharmacological interventions. 智力残疾儿童的行为挑战:药物和非药物干预的系统回顾和荟萃分析。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-27 DOI: 10.1192/bjo.2025.10871
Valerie Lye, Angela Hassiotis, Amanda Timmerman, Sohil Alqazlan, Elizaveta Dimitrova, Borbala Vegh, Vaso Totsika

Background: Behaviours that challenge are highly prevalent in children with an intellectual disability and can be detrimental to their quality of life and opportunities.

Aims: The systematic review aimed to investigate the effectiveness of current interventions in reducing behaviours that challenge in children with an intellectual disability (≤18 years-old).

Method: We searched five databases (PsychINFO, MEDLINE, Embase, Web of Science and CINAHL) on 26 April 2022 and 1 July 2024, and identified 18 randomised controlled trials (1443 participants) eligible for inclusion since 2014 - 11 investigated non-pharmacological and 9 investigated pharmacological interventions. Risk of bias was assessed using the Cochrane Risk of Bias 2 tool.

Results: Non-pharmacological interventions (mostly psychosocial) were significantly effective (Hedges' g = -0.20; 95% CI [-0.35, -0.05]), whereas pharmacological interventions (including a wide range of drug classes and substances) were not (g = 0.03; 95% CI [-0.17, 0.24]). Studies using the Child Behaviour Checklist reported significant reductions (g = -0.18; 95% CI [-0.34, -0.02]), whereas studies using the Aberrant Behaviour Checklist did not (g = 0.04; 95% CI [-0.16, 0.25]). A random-effects meta-analysis indicated no overall significant reduction in behaviours that challenge (g = -0.12; 95% CI [-0.24, 0.00]).

Conclusions: It is important to note that most studies included were conducted in Western countries and had small sample sizes, and findings may be due to the outcome measures used. Findings support current recommendations that non-pharmacological interventions should be first-line treatment for behaviours that challenge in this population. Evidence highlighted the need for better quality, adequately powered randomised controlled trials.

背景:挑战行为在智力残疾儿童中非常普遍,可能对他们的生活质量和机会有害。目的:本系统综述旨在调查当前干预措施在减少智力残疾儿童(≤18岁)挑战行为方面的有效性。方法:我们于2022年4月26日和2024年7月1日检索了5个数据库(PsychINFO、MEDLINE、Embase、Web of Science和CINAHL),并确定了自2014年以来符合纳入条件的18项随机对照试验(1443名受试者),其中11项研究非药物干预,9项研究药物干预。使用Cochrane Risk of bias 2工具评估偏倚风险。结果:非药物干预(主要是心理社会干预)显著有效(Hedges' g = -0.20; 95% CI[-0.35, -0.05]),而药物干预(包括广泛的药物类别和物质)则没有效果(g = 0.03; 95% CI[-0.17, 0.24])。使用儿童行为检查表的研究报告了显著的减少(g = -0.18; 95% CI[-0.34, -0.02]),而使用异常行为检查表的研究没有(g = 0.04; 95% CI[-0.16, 0.25])。随机效应荟萃分析显示,挑战行为总体上没有显著减少(g = -0.12; 95% CI[-0.24, 0.00])。结论:值得注意的是,大多数纳入的研究都是在西方国家进行的,样本量很小,结果可能是由于使用的结果测量。研究结果支持目前的建议,即非药物干预措施应作为对这一人群的行为挑战的一线治疗。证据强调需要更好的质量,充分支持的随机对照试验。
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引用次数: 0
The effect of Withania somnifera (Ashwagandha) on mental health symptoms in individuals with mental disorders: systematic review and meta-analysis. Withania somnifera (Ashwagandha)对精神障碍患者心理健康症状的影响:系统回顾和荟萃分析
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-27 DOI: 10.1192/bjo.2025.10885
Mattia Marchi, Pietro Grenzi, Antonio Travascio, Daniele Uberti, Edoardo De Micheli, Fabio Quartaroli, Giuseppe Laquatra, Luca Pingani, Silvia Ferrari, Gian M Galeazzi

Background: Withania somnifera (WS) is considered an adaptogen agent with reported antistress, cognition facilitating and anti-inflammatory properties, which may be beneficial in the treatment of mental disorders.

Aims: This systematic review investigated the efficacy and tolerability of Withania somnifera for mental health symptoms in individuals with mental disorders.

Method: The protocol of this review was registered with PROSPERO (CRD42023467959). PubMed, Scopus, PsycINFO, CINAHL, Embase and CENTRAL were searched for randomised controlled trials comparing Withania somnifera to any comparator, in people of any age, with any mental disorder. The meta-analyses were based on standardised mean differences (SMDs) and odds ratios with 95% confidence intervals, estimated through frequentist and Bayesian-hierarchical models with random-effects.

Results: Fourteen studies, corresponding to 360 people treated with Withania somnifera and 353 controls were included. Anxiety disorders were the predominant diagnostic category. Thirteen trials administered Withania somnifera orally (median dose 600 mg/day), one with Shirodhara therapy. The median follow-up time was 8 weeks. Although limited by the small number of studies, substantial between-study heterogeneity, and outlier effects, our investigation showed Withania somnifera effectiveness in improving anxiety (outlier-corrected SMD: -1.13 (95% CI: -1.65; -0.60), pooled SMD: -1.962 (95% CI: -2.66; -0.57)), depression (SMD: -1.28 (95% CI: -2.40; -0.16) and stress (SMD: -0.95 (95% CI: -1.46; -0.43) symptoms and sleep quality (SMD: -1.35 (95% CI: -1.79; -0.91). The effect size was confirmed using the Bayesian for anxiety but not for depression. No significant difference between Withania somnifera and the comparators was found for safety and tolerability.

Conclusions: We found evidence supporting the effectiveness of Withania somnifera in treating anxiety symptoms. Future trials should replicate this finding in larger samples and further clarify a possible Withania somnifera role in depression and insomnia treatment.

背景:Withania somnifera (WS)被认为是一种具有抗应激、促进认知和抗炎特性的适应原药物,可能有助于治疗精神障碍。目的:本系统综述探讨了Withania somnifera对精神障碍患者精神健康症状的疗效和耐受性。方法:本综述的方案在PROSPERO注册(CRD42023467959)。PubMed, Scopus, PsycINFO, CINAHL, Embase和CENTRAL检索了在任何年龄,任何精神障碍的人群中比较Withania somnifera与任何比较物的随机对照试验。meta分析基于标准化平均差异(SMDs)和95%置信区间的优势比,通过随机效应的频率模型和贝叶斯分层模型估计。结果:纳入了14项研究,对应于360例用Withania somnifera治疗的患者和353例对照。焦虑障碍是主要的诊断类别。13项试验口服Withania somnifera(中位剂量600mg /天),1项试验采用Shirodhara疗法。中位随访时间为8周。尽管受到研究数量少、研究间异质性和异常值效应的限制,我们的调查显示,草藤在改善焦虑(异常值校正SMD: -1.13 (95% CI: -1.65; -0.60)、综合SMD: -1.962 (95% CI: -2.66; -0.57)、抑郁(SMD: -1.28 (95% CI: -2.40; -0.16)和压力(SMD: -0.95 (95% CI: -1.46; -0.43)症状和睡眠质量(SMD: -1.35 (95% CI: -1.79; -0.91)方面有效。使用贝叶斯方法证实了焦虑的效应量,但对抑郁没有效果。在安全性和耐受性方面,与对照品无显著差异。结论:我们发现的证据支持Withania somnifera治疗焦虑症状的有效性。未来的试验应该在更大的样本中重复这一发现,并进一步阐明睡眠Withania在抑郁症和失眠治疗中的可能作用。
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引用次数: 0
Validation of the 12-item World Health Organization Disability Assessment Schedule (WHODAS 2.0) in adults with attention-deficit hyperactivity disorder. 12项世界卫生组织残疾评估表(WHODAS 2.0)在成人注意缺陷多动障碍中的验证
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-27 DOI: 10.1192/bjo.2025.10873
Silvia Amoretti, Juan Jesús Crespín, Montse Corrales, Carla Torrent, Derek Clougher, Santiago Biel, Carolina Ramos-Sayalero, Pol Ibáñez, Ferran Mestres, Christian Fadeuilhe, Vanesa Richarte, Josep Antoni Ramos-Quiroga

Background: Attention deficit hyperactivity disorder (ADHD) is often associated with psychosocial functioning difficulties and valid measures of disability are needed for this population. The 12-item World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0) is widely used to measure disability but has not been validated in the adult ADHD population.

Aims: This study aims to assess the psychometric properties of the WHODAS 2.0 in adults with ADHD, and to examine differences in disability levels between ADHD subtypes and gender.

Method: A cross-sectional study was conducted with 577 adults with ADHD (mean age: 38.24, s.d = 12.23; 52.3% male). ADHD severity was assessed using the ADHD Rating Scale (ADHD-RS) and Clinical Global Impression-Severity (CGI-S) Scale, while functionality was measured with the WHODAS 2.0 and the Functioning Assessment Short Test (FAST). Analyses included: (a) Cronbach's α for internal consistency, (b) Pearson's correlation for convergent validity, (c) Confirmatory Factor Analysis (CFA) for factor structure and (d) t-tests to compare disability levels across ADHD subtypes and gender.

Results: The WHODAS 2.0 demonstrated good internal consistency (Cronbach's α = 0.89). Scores were significantly correlated with psychosocial functioning (FAST, r = 0.476, p < 0.001) and clinical measures. CFA supported the original six-factor structure (root mean square error of approximation 0.039, Comparative Fit Index 0.998, Tucker-Lewis Index 0.996). When comparing ADHD subtypes, participants with the combined subtype had higher WHODAS 2.0 total scores than those with the inattentive subtype (p = 0.006). Additionally, gender differences were identified, with females displaying higher disability levels (p = 0.005).

Conclusions: The WHODAS 2.0 demonstrates psychometric properties that suggest it is a valid and reliable tool for assessing disability in adults with ADHD.

背景:注意缺陷多动障碍(ADHD)通常与社会心理功能困难有关,需要对这一人群进行有效的残疾测量。世界卫生组织的12项残疾评估表2.0 (WHODAS 2.0)被广泛用于衡量残疾,但尚未在成年ADHD人群中得到验证。目的:本研究旨在评估成人ADHD患者WHODAS 2.0的心理测量特性,并研究ADHD亚型和性别之间残疾水平的差异。方法:对577例成人ADHD患者进行横断面研究,平均年龄38.24岁,s.d = 12.23,男性占52.3%。使用ADHD评定量表(ADHD- rs)和临床总体印象严重程度量表(CGI-S)评估ADHD严重程度,使用WHODAS 2.0和功能评估短测试(FAST)测量功能。分析包括:(a)内部一致性的Cronbach's α, (b)收敛效度的Pearson's相关性,(c)因素结构的验证性因子分析(CFA)和(d)比较不同ADHD亚型和性别的残疾水平的t检验。结果:WHODAS 2.0具有良好的内部一致性(Cronbach’s α = 0.89)。得分与心理社会功能(FAST, r = 0.476, p < 0.001)和临床措施显著相关。CFA支持原始的六因子结构(近似均方根误差0.039,比较拟合指数0.998,Tucker-Lewis指数0.996)。当比较ADHD亚型时,合并亚型的参与者的WHODAS 2.0总分高于注意力不集中亚型(p = 0.006)。此外,性别差异被确定,女性表现出更高的残疾水平(p = 0.005)。结论:WHODAS 2.0显示了心理测量特性,表明它是评估成人ADHD残疾的有效和可靠的工具。
{"title":"Validation of the 12-item World Health Organization Disability Assessment Schedule (WHODAS 2.0) in adults with attention-deficit hyperactivity disorder.","authors":"Silvia Amoretti, Juan Jesús Crespín, Montse Corrales, Carla Torrent, Derek Clougher, Santiago Biel, Carolina Ramos-Sayalero, Pol Ibáñez, Ferran Mestres, Christian Fadeuilhe, Vanesa Richarte, Josep Antoni Ramos-Quiroga","doi":"10.1192/bjo.2025.10873","DOIUrl":"10.1192/bjo.2025.10873","url":null,"abstract":"<p><strong>Background: </strong>Attention deficit hyperactivity disorder (ADHD) is often associated with psychosocial functioning difficulties and valid measures of disability are needed for this population. The 12-item World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0) is widely used to measure disability but has not been validated in the adult ADHD population.</p><p><strong>Aims: </strong>This study aims to assess the psychometric properties of the WHODAS 2.0 in adults with ADHD, and to examine differences in disability levels between ADHD subtypes and gender.</p><p><strong>Method: </strong>A cross-sectional study was conducted with 577 adults with ADHD (mean age: 38.24, s.d = 12.23; 52.3% male). ADHD severity was assessed using the ADHD Rating Scale (ADHD-RS) and Clinical Global Impression-Severity (CGI-S) Scale, while functionality was measured with the WHODAS 2.0 and the Functioning Assessment Short Test (FAST). Analyses included: (a) Cronbach's <i>α</i> for internal consistency, (b) Pearson's correlation for convergent validity, (c) Confirmatory Factor Analysis (CFA) for factor structure and (d) <i>t</i>-tests to compare disability levels across ADHD subtypes and gender.</p><p><strong>Results: </strong>The WHODAS 2.0 demonstrated good internal consistency (Cronbach's <i>α</i> = 0.89). Scores were significantly correlated with psychosocial functioning (FAST, <i>r</i> = 0.476, <i>p</i> < 0.001) and clinical measures. CFA supported the original six-factor structure (root mean square error of approximation 0.039, Comparative Fit Index 0.998, Tucker-Lewis Index 0.996). When comparing ADHD subtypes, participants with the combined subtype had higher WHODAS 2.0 total scores than those with the inattentive subtype (<i>p</i> = 0.006). Additionally, gender differences were identified, with females displaying higher disability levels (<i>p</i> = 0.005).</p><p><strong>Conclusions: </strong>The WHODAS 2.0 demonstrates psychometric properties that suggest it is a valid and reliable tool for assessing disability in adults with ADHD.</p>","PeriodicalId":9038,"journal":{"name":"BJPsych Open","volume":"11 6","pages":"e257"},"PeriodicalIF":3.5,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12569619/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145372127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improving Women's Sexual and Reproductive Health in a Psychiatric Inpatient Setting Quality Improvement Project: Development and Implementation of a Women's Physical Health Clinic in a Psychiatric Hospital in North London - CORRIGENDUM. 在精神病住院环境中改善妇女的性健康和生殖健康质量改进项目:伦敦北部一家精神病医院妇女身体健康诊所的发展和实施-勘误表。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-27 DOI: 10.1192/bjo.2025.10906
Chiara Petrosellini, Pollyanna Cohen, Monika Gorny, Paul Gyimah, Tomilola James, Neil Sarkar, Saira Chowdhary
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引用次数: 0
The association between financial strain, psychological distress and subsequent depression: findings from a Norwegian national study. 经济压力、心理困扰和随后的抑郁之间的联系:来自挪威国家研究的发现。
IF 3.5 3区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-24 DOI: 10.1192/bjo.2025.10878
Børge Sivertsen, Mari Hysing, Tormod Bøe

Background: Financial strain is increasingly recognised as a contributor to psychological distress, which may in turn elevate the risk of developing mental disorder. However, few large-scale longitudinal studies have investigated its predictive role using diagnostic outcomes among higher education students.

Aims: To examine whether financial strain predicts a major depressive episode (MDE) one year later among Norwegian students, and whether associations are explained by sociodemographic factors or baseline psychological distress.

Method: Data were drawn from the national Students' Health and Wellbeing Study 2022 (SHoT2022) survey (N = 53 362), with a diagnostic follow-up one year later (N = 10 460) using the self-administered Composite International Diagnostic Interview version 5.0 (CIDI 5.0). Inverse probability weighted Poisson regression with robust standard errors estimated the risk of 30-day DSM-5-defined MDE for each financial indicator.

Results: Financial strain was widespread: 6% reported frequent financial difficulties, 27% were unable to cover an emergency expense of 5000 Norwegian kroner (NOK; approximately €450/$500, and 35% spent 60% or more of their income on housing. Several indicators significantly predicted later MDE. Students frequently experiencing financial difficulties had a 3.55-fold increased risk (95% CI:2.97-4.22), attenuating to 1.53 (1.28-1.83) after full adjustment. Similar patterns emerged for most indicators. Associations were largely unaffected by sociodemographic adjustment, but were substantially reduced after accounting for baseline psychological distress.

Conclusions: Financial strain was associated with increased risk of MDE one year later, although much of the association was explained by baseline distress. Policies should address both financial and psychological vulnerabilities through strengthened financial support, alignment with living costs and targeted measures such as financial counselling and housing assistance.

背景:越来越多的人认为经济压力是造成心理困扰的一个因素,而心理困扰又可能增加患精神障碍的风险。然而,很少有大规模的纵向研究利用高等教育学生的诊断结果来调查其预测作用。目的:研究经济压力是否可以预测挪威学生一年后的重度抑郁发作(MDE),以及这种关联是否可以用社会人口因素或基线心理困扰来解释。方法:数据来自全国学生健康与幸福研究2022 (SHoT2022)调查(N = 53 362),并在一年后使用自我管理的综合国际诊断访谈5.0版(CIDI 5.0)进行诊断随访(N = 10 460)。具有稳健标准误差的逆概率加权泊松回归估计了dsm -5定义的30天MDE对每个财务指标的风险。结果:资金紧张很普遍:6%的人报告经常出现财务困难,27%的人无法支付5000挪威克朗(挪威克朗;约450欧元/ 500美元)的紧急费用,35%的人将其收入的60%或更多用于住房。有几个指标显著地预测了MDE。经常经历经济困难的学生的风险增加了3.55倍(95% CI:2.97-4.22),在完全调整后降低到1.53(1.28-1.83)。大多数指标也出现了类似的模式。关联在很大程度上不受社会人口调整的影响,但在考虑了基线心理困扰后,关联显著减少。结论:经济压力与一年后MDE风险增加有关,尽管大部分关联可以用基线窘迫来解释。政策应通过加强财政支持、与生活成本保持一致以及财务咨询和住房援助等有针对性的措施,解决经济和心理脆弱性问题。
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引用次数: 0
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BJPsych Open
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