Pub Date : 2026-01-31DOI: 10.1186/s13643-026-03078-0
Buddheera W M B Kumburegama, Andreas T Kristensen, Goran Bjelakovic, Dimitrinka Nikolova, Mark A Asante, Milica Bjelakovic, Ronald L Koretz, Mithuna M Balakumar, Martin E Michelsen, Sarah L Klingenberg, Christian Gluud
Background: Chronic hepatitis C virus infection presents a substantial global health burden, frequently resulting in severe liver conditions. Hepatitis C virus (HCV) therapy requires complex decision-making. Direct-acting antivirals (DAAs) offer a potential solution by targeting viral proteins to inhibit replication. Understanding DAAs real-world effectiveness and how they impact long-term outcomes beyond clinical trials is essential. We aim to comprehensively evaluate the benefits and harms of DAAs in individuals with chronic HCV infection, reported in observational studies.
Methods: We will consider for inclusion prospective and retrospective observational studies with quasi-randomised, cohort, case-control, controlled before-and-after, and cross-sectional designs. Our experimental interventions will be any class of DAAs available on the market or in development. DAAs could have been administered alone, in combination, or with other medical co-interventions. Our control interventions will be untreated chronic HCV conditions, with or without placebo. Participants will be adults, regardless of demographics, treatment history, or healthcare setting. Our primary outcomes will be participants experiencing hepatitis C-related morbidity or all-cause mortality, serious adverse events, and health-related quality of life. Secondary outcomes will include all-cause mortality, cirrhosis, variceal bleeding, hepato-renal syndrome, hepatocellular carcinoma, hepatic encephalopathy, non-serious adverse events, liver transplantation, lack of sustained virological response, histological improvement, and decreases in alanine aminotransferase and aspartate aminotransferase levels. We will apply search strategies to search MEDLINE, Embase, Web of Science, grey literature, and trial registers. We will use Covidence® to screen the result, including citations. Individual double-data extraction will include study details and outcomes, with independent review authors resolving discrepancies. We will assess bias using the ROBINS-I tool. Meta-analyses will employ random-effects models for both dichotomous and continuous outcomes, assessing heterogeneity. Subgroup and sensitivity analyses will explore effect modifications and address missing data. Trial Sequential Analysis will control type I and type II errors. We will evaluate publication bias using funnel plots and Egger's regression test and assess certainty of evidence using GRADE.
Discussion: The findings will inform clinical decisions and benefit those affected by HCV, healthcare professionals, and policymakers.
背景:慢性丙型肝炎病毒感染是一个重大的全球健康负担,经常导致严重的肝脏疾病。丙型肝炎病毒(HCV)治疗需要复杂的决策。直接作用抗病毒药物(DAAs)通过靶向病毒蛋白抑制复制提供了一种潜在的解决方案。了解daa的实际有效性以及它们如何影响临床试验之外的长期结果是至关重要的。我们的目的是全面评估观察性研究中报道的DAAs对慢性HCV感染患者的益处和危害。方法:我们将考虑纳入准随机、队列、病例对照、前后对照和横断面设计的前瞻性和回顾性观察性研究。我们的实验性干预措施将是市场上可用或正在开发的任何类别的daa。DAAs可以单独使用,也可以联合使用,也可以与其他医疗联合干预措施一起使用。我们的对照干预措施将是未经治疗的慢性HCV疾病,使用或不使用安慰剂。参与者将是成年人,无论人口统计学、治疗史或医疗环境如何。我们的主要结局是参与者的丙型肝炎相关发病率或全因死亡率、严重不良事件和与健康相关的生活质量。次要结局包括全因死亡率、肝硬化、静脉曲张出血、肝肾综合征、肝细胞癌、肝性脑病、非严重不良事件、肝移植、缺乏持续病毒学反应、组织学改善、谷丙转氨酶和天冬氨酸转氨酶水平降低。我们将应用搜索策略来搜索MEDLINE, Embase, Web of Science,灰色文献和试验注册。我们将使用covid®筛选结果,包括引文。单独的双数据提取将包括研究细节和结果,由独立的综述作者解决差异。我们将使用ROBINS-I工具评估偏倚。荟萃分析将采用随机效应模型来评估二分类和连续结果的异质性。分组和敏感性分析将探讨效果修改和解决缺失数据。试验序贯分析将控制第一类和第二类错误。我们将使用漏斗图和Egger回归检验评估发表偏倚,并使用GRADE评估证据的确定性。讨论:研究结果将为临床决策提供信息,并使HCV患者、卫生保健专业人员和政策制定者受益。系统评价注册:PROSPERO: CRD42023494844。
{"title":"Direct-acting antivirals for chronic hepatitis C infection: a protocol for a systematic review of observational studies.","authors":"Buddheera W M B Kumburegama, Andreas T Kristensen, Goran Bjelakovic, Dimitrinka Nikolova, Mark A Asante, Milica Bjelakovic, Ronald L Koretz, Mithuna M Balakumar, Martin E Michelsen, Sarah L Klingenberg, Christian Gluud","doi":"10.1186/s13643-026-03078-0","DOIUrl":"https://doi.org/10.1186/s13643-026-03078-0","url":null,"abstract":"<p><strong>Background: </strong>Chronic hepatitis C virus infection presents a substantial global health burden, frequently resulting in severe liver conditions. Hepatitis C virus (HCV) therapy requires complex decision-making. Direct-acting antivirals (DAAs) offer a potential solution by targeting viral proteins to inhibit replication. Understanding DAAs real-world effectiveness and how they impact long-term outcomes beyond clinical trials is essential. We aim to comprehensively evaluate the benefits and harms of DAAs in individuals with chronic HCV infection, reported in observational studies.</p><p><strong>Methods: </strong>We will consider for inclusion prospective and retrospective observational studies with quasi-randomised, cohort, case-control, controlled before-and-after, and cross-sectional designs. Our experimental interventions will be any class of DAAs available on the market or in development. DAAs could have been administered alone, in combination, or with other medical co-interventions. Our control interventions will be untreated chronic HCV conditions, with or without placebo. Participants will be adults, regardless of demographics, treatment history, or healthcare setting. Our primary outcomes will be participants experiencing hepatitis C-related morbidity or all-cause mortality, serious adverse events, and health-related quality of life. Secondary outcomes will include all-cause mortality, cirrhosis, variceal bleeding, hepato-renal syndrome, hepatocellular carcinoma, hepatic encephalopathy, non-serious adverse events, liver transplantation, lack of sustained virological response, histological improvement, and decreases in alanine aminotransferase and aspartate aminotransferase levels. We will apply search strategies to search MEDLINE, Embase, Web of Science, grey literature, and trial registers. We will use Covidence® to screen the result, including citations. Individual double-data extraction will include study details and outcomes, with independent review authors resolving discrepancies. We will assess bias using the ROBINS-I tool. Meta-analyses will employ random-effects models for both dichotomous and continuous outcomes, assessing heterogeneity. Subgroup and sensitivity analyses will explore effect modifications and address missing data. Trial Sequential Analysis will control type I and type II errors. We will evaluate publication bias using funnel plots and Egger's regression test and assess certainty of evidence using GRADE.</p><p><strong>Discussion: </strong>The findings will inform clinical decisions and benefit those affected by HCV, healthcare professionals, and policymakers.</p><p><strong>Systematic review registration: </strong>PROSPERO: CRD42023494844.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146094055","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Depression and anxiety are among the most common mental health problems affecting children and adolescents worldwide. Exercise is a widely used and potentially cost-effective non-pharmacological approach that may improve mood and mental health. However, the optimal exercise modalities and doses for alleviating depressive and anxiety symptoms in children and adolescents remain uncertain. Previous evidence has primarily relied on pairwise meta-analyses or conventional network meta-analyses: the former are unable to compare multiple exercise formats simultaneously, while the latter, although capable of integrating different interventions, have not quantified dose characteristics such as intensity, frequency, and duration. Consequently, systematic dose-response evidence regarding depressive and anxiety symptoms in children and adolescents is lacking. This study aims to examine the quantitative relationship between exercise dose and changes in depressive and anxiety symptoms.
Methods: This protocol outlines a systematic review and Bayesian model-based dose-response network meta-analysis. A systematic search will be conducted of PubMed, Embase, Web of Science, the Cochrane Library, Scopus, PsycINFO, SPORTDiscus, and the China National Knowledge Infrastructure databases through May 2026. Randomized controlled trials enrolling children and adolescents aged 6-18 years with depressive or anxiety symptoms and comparing different types and doses of exercise training will be eligible for inclusion. Study quality will be appraised using the Cochrane Risk of Bias 2.0 tool. Exercise interventions will be categorized by type (e.g., aerobic, resistance, mind-body, and combined exercise-only) prior to dose-response modeling. A Bayesian model-based dose-response network meta-analysis will be performed, with exercise dose quantified as weekly metabolic equivalent of task (MET) minutes (MET-min/week) by integrating intensity, session duration, and frequency. Nonlinear dose-response curves will be fitted for distinct exercise modalities. Meta-classification and regression tree (meta-CART) analysis will be employed to identify potential effect modifiers.
Discussion: This study will systematically evaluate the nonlinear dose-response relationships between exercise dose and changes in depressive and anxiety symptoms in children and adolescents, and estimate dose ranges associated with symptom change across exercise modalities. The findings may help inform future evidence-based recommendations and provide methodological guidance for dose-response research in child and adolescent mental health.
Systematic review registration: This protocol has been registered with the International Prospective Register of Systematic Reviews (PROSPERO), registration number CRD420251174947.
背景:抑郁和焦虑是影响全世界儿童和青少年的最常见的心理健康问题。运动是一种广泛使用且具有潜在成本效益的非药物方法,可以改善情绪和心理健康。然而,缓解儿童和青少年抑郁和焦虑症状的最佳运动方式和剂量仍然不确定。以前的证据主要依赖于两两荟萃分析或传统的网络荟萃分析:前者无法同时比较多种运动形式,而后者虽然能够整合不同的干预措施,但没有量化剂量特征,如强度、频率和持续时间。因此,缺乏关于儿童和青少年抑郁和焦虑症状的系统剂量反应证据。本研究旨在探讨运动剂量与抑郁和焦虑症状变化之间的定量关系。方法:本方案概述了系统综述和基于贝叶斯模型的剂量-反应网络荟萃分析。到2026年5月,将对PubMed、Embase、Web of Science、Cochrane Library、Scopus、PsycINFO、SPORTDiscus和中国国家知识基础设施数据库进行系统检索。纳入有抑郁或焦虑症状的6-18岁儿童和青少年,并比较不同类型和剂量的运动训练的随机对照试验将符合纳入条件。研究质量将使用Cochrane风险偏倚2.0工具进行评价。在剂量-反应建模之前,运动干预将按类型(例如,有氧,阻力,身心和综合运动)进行分类。将进行基于贝叶斯模型的剂量-反应网络荟萃分析,通过整合强度、运动持续时间和频率,将运动剂量量化为每周代谢当量任务(MET)分钟(MET-min/week)。非线性剂量-反应曲线将适合不同的运动模式。Meta-classification and regression tree (meta-CART)分析将用于识别潜在的效果修饰因子。讨论:本研究将系统地评估运动剂量与儿童和青少年抑郁和焦虑症状变化之间的非线性剂量-反应关系,并估计不同运动方式下与症状变化相关的剂量范围。这些发现可能有助于为未来的循证建议提供信息,并为儿童和青少年心理健康的剂量反应研究提供方法学指导。系统评价注册:本方案已在国际前瞻性系统评价注册(PROSPERO)注册,注册号为CRD420251174947。
{"title":"Optimal exercise prescription for depression and anxiety in children and adolescents: a Bayesian dose-response network meta-analysis protocol.","authors":"Wanli Zang, Jiarong Wu, Na Liu, Mingqing Fang, Ningkun Xiao, Jingtao Wu, Jia Liu, Qiuxia Zhang","doi":"10.1186/s13643-026-03075-3","DOIUrl":"https://doi.org/10.1186/s13643-026-03075-3","url":null,"abstract":"<p><strong>Background: </strong>Depression and anxiety are among the most common mental health problems affecting children and adolescents worldwide. Exercise is a widely used and potentially cost-effective non-pharmacological approach that may improve mood and mental health. However, the optimal exercise modalities and doses for alleviating depressive and anxiety symptoms in children and adolescents remain uncertain. Previous evidence has primarily relied on pairwise meta-analyses or conventional network meta-analyses: the former are unable to compare multiple exercise formats simultaneously, while the latter, although capable of integrating different interventions, have not quantified dose characteristics such as intensity, frequency, and duration. Consequently, systematic dose-response evidence regarding depressive and anxiety symptoms in children and adolescents is lacking. This study aims to examine the quantitative relationship between exercise dose and changes in depressive and anxiety symptoms.</p><p><strong>Methods: </strong>This protocol outlines a systematic review and Bayesian model-based dose-response network meta-analysis. A systematic search will be conducted of PubMed, Embase, Web of Science, the Cochrane Library, Scopus, PsycINFO, SPORTDiscus, and the China National Knowledge Infrastructure databases through May 2026. Randomized controlled trials enrolling children and adolescents aged 6-18 years with depressive or anxiety symptoms and comparing different types and doses of exercise training will be eligible for inclusion. Study quality will be appraised using the Cochrane Risk of Bias 2.0 tool. Exercise interventions will be categorized by type (e.g., aerobic, resistance, mind-body, and combined exercise-only) prior to dose-response modeling. A Bayesian model-based dose-response network meta-analysis will be performed, with exercise dose quantified as weekly metabolic equivalent of task (MET) minutes (MET-min/week) by integrating intensity, session duration, and frequency. Nonlinear dose-response curves will be fitted for distinct exercise modalities. Meta-classification and regression tree (meta-CART) analysis will be employed to identify potential effect modifiers.</p><p><strong>Discussion: </strong>This study will systematically evaluate the nonlinear dose-response relationships between exercise dose and changes in depressive and anxiety symptoms in children and adolescents, and estimate dose ranges associated with symptom change across exercise modalities. The findings may help inform future evidence-based recommendations and provide methodological guidance for dose-response research in child and adolescent mental health.</p><p><strong>Systematic review registration: </strong>This protocol has been registered with the International Prospective Register of Systematic Reviews (PROSPERO), registration number CRD420251174947.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146087306","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Acute lymphoblastic leukemia (ALL) is a hematologic malignancy characterized by malignant transformation of lymphoid precursor cells. ALL prognosis differs considerably, especially between pediatric patients and adult patients, with poor response to therapy in adults. MicroRNAs (miRNAs), small non-coding RNAs that regulate the expression of genes, are possible cancer biomarkers that predict cancer prognosis. This systematic review and meta-analysis evaluates miRNAs as prognostic biomarkers in ALL and extends the findings through ceRNA network and single-cell RNA seq analyses of validated target genes.
Material and methods: We systematically searched PubMed, SCOPUS, and Web of Science (WOS) to identify studies that compared miRNA expression with the survival of ALL patients following the PRISMA guidelines. We reviewed these studies for their methodological quality, and hazard ratios (HRs) were extracted to examine miRNA expression and survival endpoints of overall survival (OS), disease-free survival (DFS), and relapse-free survival (RFS). We also applied single-cell RNA sequencing (scRNA-seq) and a competing endogenous RNA (ceRNA) network to study miRNA targets.
Results: miR-335 showed a significant protective role with a pooled HR of 0.29 (95% CI, 0.12-0.68), miR-210 with a pooled HR of 0.22 (95% CI, 0.06-0.84), and miR-125b with a pooled HR of 0.39 (95% CI, 0.16-0.95) based on 22 examined studies involving 1974 patients. These miRNAs were correlated with improved OS, DFS, and RFS. We identified potential targets, whose functions were examined within key biological pathways through a ceRNA network. In various immune cell types, comparisons of B-ALL and T-ALL with normal cells showed that 36 and 98 target genes, respectively, were upregulated, while 21 and 19 genes were downregulated. Additionally, when comparing T-ALL to B-ALL cells, 70 target genes had increased expression, and 13 genes had decreased expression. Among all analyzed lineages, leukemic blast cells exhibited the most consistent and pronounced alterations in the expression of validated miRNA target genes, suggesting that blasts are the primary population influenced by these regulatory interactions in ALL.
Conclusion: These findings support miRNAs as valuable prognostic biomarkers for ALL with potential for personalized therapy. The context-dependent role of these miRNAs highlights the need for confirmation through large, multicenter trials. The constructed ceRNA network provides useful insights into their regulatory mechanisms, opening new directions for therapeutic strategies.
{"title":"MicroRNAs as potential prognostic biomarkers in acute lymphoblastic leukemia: a systematic review, meta-analysis, and bioinformatics study.","authors":"Samaneh Toutounchian, Kiyarash Behboodi, Mona Alinejadfard, Parmida Bagheri, Maedeh Mohaghegh, Kasra Izadpanahi, Fatemeh Mohagheghian, Najmeh Salehi, Zahra Eghbali, Zahra Salehi","doi":"10.1186/s13643-026-03083-3","DOIUrl":"https://doi.org/10.1186/s13643-026-03083-3","url":null,"abstract":"<p><strong>Background: </strong>Acute lymphoblastic leukemia (ALL) is a hematologic malignancy characterized by malignant transformation of lymphoid precursor cells. ALL prognosis differs considerably, especially between pediatric patients and adult patients, with poor response to therapy in adults. MicroRNAs (miRNAs), small non-coding RNAs that regulate the expression of genes, are possible cancer biomarkers that predict cancer prognosis. This systematic review and meta-analysis evaluates miRNAs as prognostic biomarkers in ALL and extends the findings through ceRNA network and single-cell RNA seq analyses of validated target genes.</p><p><strong>Material and methods: </strong>We systematically searched PubMed, SCOPUS, and Web of Science (WOS) to identify studies that compared miRNA expression with the survival of ALL patients following the PRISMA guidelines. We reviewed these studies for their methodological quality, and hazard ratios (HRs) were extracted to examine miRNA expression and survival endpoints of overall survival (OS), disease-free survival (DFS), and relapse-free survival (RFS). We also applied single-cell RNA sequencing (scRNA-seq) and a competing endogenous RNA (ceRNA) network to study miRNA targets.</p><p><strong>Results: </strong>miR-335 showed a significant protective role with a pooled HR of 0.29 (95% CI, 0.12-0.68), miR-210 with a pooled HR of 0.22 (95% CI, 0.06-0.84), and miR-125b with a pooled HR of 0.39 (95% CI, 0.16-0.95) based on 22 examined studies involving 1974 patients. These miRNAs were correlated with improved OS, DFS, and RFS. We identified potential targets, whose functions were examined within key biological pathways through a ceRNA network. In various immune cell types, comparisons of B-ALL and T-ALL with normal cells showed that 36 and 98 target genes, respectively, were upregulated, while 21 and 19 genes were downregulated. Additionally, when comparing T-ALL to B-ALL cells, 70 target genes had increased expression, and 13 genes had decreased expression. Among all analyzed lineages, leukemic blast cells exhibited the most consistent and pronounced alterations in the expression of validated miRNA target genes, suggesting that blasts are the primary population influenced by these regulatory interactions in ALL.</p><p><strong>Conclusion: </strong>These findings support miRNAs as valuable prognostic biomarkers for ALL with potential for personalized therapy. The context-dependent role of these miRNAs highlights the need for confirmation through large, multicenter trials. The constructed ceRNA network provides useful insights into their regulatory mechanisms, opening new directions for therapeutic strategies.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146087285","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1186/s13643-025-03055-z
Matheesha Herath, Scarlotte Kulas, Jessie Martin, Ellie C Treloar, Jesse D Ey, Emma L Bradshaw, Jarrod DeSilva-White, Suzanne Edwards, Martin Bruening, Guy J Maddern
Background: Human behavioural research is often clouded with the risk that study results may be contaminated by the participant's awareness that they are being observed. Direct observation by a person is associated with this phenomenon, but limited data exists evaluating this Hawthorne Effect when less invasive video recording devices are used. Here we present the first quantitative analysis to identify the extent to which this occurs, based on self-reported behavioural change when cameras are used.
Methods: Searches of MEDLINE, Embase, Emcare, PsycINFO, CINAHL, and Google Scholar were performed on 01/12/2022. No limitations were set. The primary outcome was the proportion of participants who changed their behaviour due to awareness of being recorded. Two blinded reviewers performed screening in accordance with PRISMA guidelines. I2 statistic was used to assess for heterogeneity and a random effects model was subsequently applied for the meta-analysis.
Results: Preliminary searches identified 1728 publications. After screening, twenty-eight studies were included in the final analysis involving 2586 participants. Nine publications were suitable for quantitative analysis of the primary outcome. Pooled analysis using a random-effects model demonstrated the proportion of participants who reported behavioural change because of the camera was 15% (95% CI 0.08, 0.23) [I2 = 96.16%].
Conclusion: The presence of a video camera may cause behavioural change in a small proportion of study participants. Cameras may cause a much lower rate of reactivity compared to a direct human observer. The heterogeneity and high risk of bias of the publications highlight the need for further high-quality research into this subject area.
背景:人类行为研究常常被这样一种风险所笼罩,即研究结果可能因参与者意识到自己正在被观察而受到污染。一个人的直接观察与这种现象有关,但是当使用侵入性较小的视频记录设备时,评估这种霍桑效应的数据有限。在这里,我们提出了第一个定量分析,以确定这种情况发生的程度,基于使用相机时自我报告的行为变化。方法:于2022年12月1日检索MEDLINE、Embase、Emcare、PsycINFO、CINAHL和谷歌Scholar。没有设定任何限制。主要结果是由于意识到被记录而改变行为的参与者的比例。两名盲法审稿人按照PRISMA指南进行筛选。采用I2统计量评估异质性,随后采用随机效应模型进行meta分析。结果:初步检索确定了1728份出版物。筛选后,28项研究纳入最终分析,涉及2586名参与者。9篇出版物适合用于主要结局的定量分析。使用随机效应模型的汇总分析显示,由于照相机而报告行为改变的参与者比例为15% (95% CI 0.08, 0.23) [I2 = 96.16%]。结论:摄像机的存在可能会导致一小部分研究参与者的行为改变。与直接的人类观察者相比,相机可能会引起更低的反应率。出版物的异质性和高偏倚风险突出了对该主题领域进行进一步高质量研究的必要性。系统评价注册:PROSPERO CRD42022370498。
{"title":"Evaluating the impact of video cameras on participant behaviour in research: a systematic review and meta-analysis.","authors":"Matheesha Herath, Scarlotte Kulas, Jessie Martin, Ellie C Treloar, Jesse D Ey, Emma L Bradshaw, Jarrod DeSilva-White, Suzanne Edwards, Martin Bruening, Guy J Maddern","doi":"10.1186/s13643-025-03055-z","DOIUrl":"https://doi.org/10.1186/s13643-025-03055-z","url":null,"abstract":"<p><strong>Background: </strong>Human behavioural research is often clouded with the risk that study results may be contaminated by the participant's awareness that they are being observed. Direct observation by a person is associated with this phenomenon, but limited data exists evaluating this Hawthorne Effect when less invasive video recording devices are used. Here we present the first quantitative analysis to identify the extent to which this occurs, based on self-reported behavioural change when cameras are used.</p><p><strong>Methods: </strong>Searches of MEDLINE, Embase, Emcare, PsycINFO, CINAHL, and Google Scholar were performed on 01/12/2022. No limitations were set. The primary outcome was the proportion of participants who changed their behaviour due to awareness of being recorded. Two blinded reviewers performed screening in accordance with PRISMA guidelines. I<sup>2</sup> statistic was used to assess for heterogeneity and a random effects model was subsequently applied for the meta-analysis.</p><p><strong>Results: </strong>Preliminary searches identified 1728 publications. After screening, twenty-eight studies were included in the final analysis involving 2586 participants. Nine publications were suitable for quantitative analysis of the primary outcome. Pooled analysis using a random-effects model demonstrated the proportion of participants who reported behavioural change because of the camera was 15% (95% CI 0.08, 0.23) [I<sup>2</sup> = 96.16%].</p><p><strong>Conclusion: </strong>The presence of a video camera may cause behavioural change in a small proportion of study participants. Cameras may cause a much lower rate of reactivity compared to a direct human observer. The heterogeneity and high risk of bias of the publications highlight the need for further high-quality research into this subject area.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD42022370498.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146041782","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1186/s13643-026-03072-6
Carole Délétroz, Marina Canepa Allen, Achille R Yameogo, Maxime Sasseville, Florian Naye, Alexandra Rouquette, Patrick Bodenmann, Marie-Pierre Gagnon
Background: This study aimed to systematically identify, synthesize, and evaluate measurement properties of patient-reported outcome measures (PROMs) of eHL in adult populations.
Method: A systematic review was conducted, considering studies reporting the development or validation of eHL instruments for adult populations. Four databases and grey literature were searched from January 2000 to 2024, with additional website searches up to 2022. Quality assessment, data analysis and synthesis followed the COSMIN methodology and findings were reported according to PRISMA 2020 guidelines. The GRADE framework was used to assess evidence quality.
Results: A total of 8558 citations were identified. Seven instruments, 89 articles and 3 reports were included in this review. The HL19-DIGI, DHLI, TeHLI, eHLQ, eHLA, and Lisane demonstrated sufficient ratings for aspects of content validity, albeit with varying levels of evidence, ranging from very low to high. Five instruments showed sufficient ratings for structural validity and internal consistency, but evidence on their reliability was insufficient. No information on responsiveness was mentioned in articles. The HL19-DIGI, DHLI, eHEALS, and eHLQ were the most frequently investigated instruments.
Conclusion: This review identified 17 eHL instruments, of which seven demonstrated adequate content validity. However, insufficient evidence exists regarding psychometric properties for widespread implementation. It is strongly recommended that the content of these instruments be updated to reflect patients' evolving use of eHealth services, and that further psychometrics evaluations be conducted systematically.
{"title":"Systematic review of the measurement properties of patient-reported outcome measures (PROMs) of eHealth literacy in adult populations.","authors":"Carole Délétroz, Marina Canepa Allen, Achille R Yameogo, Maxime Sasseville, Florian Naye, Alexandra Rouquette, Patrick Bodenmann, Marie-Pierre Gagnon","doi":"10.1186/s13643-026-03072-6","DOIUrl":"https://doi.org/10.1186/s13643-026-03072-6","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to systematically identify, synthesize, and evaluate measurement properties of patient-reported outcome measures (PROMs) of eHL in adult populations.</p><p><strong>Method: </strong>A systematic review was conducted, considering studies reporting the development or validation of eHL instruments for adult populations. Four databases and grey literature were searched from January 2000 to 2024, with additional website searches up to 2022. Quality assessment, data analysis and synthesis followed the COSMIN methodology and findings were reported according to PRISMA 2020 guidelines. The GRADE framework was used to assess evidence quality.</p><p><strong>Results: </strong>A total of 8558 citations were identified. Seven instruments, 89 articles and 3 reports were included in this review. The HL<sub>19</sub>-DIGI, DHLI, TeHLI, eHLQ, eHLA, and Lisane demonstrated sufficient ratings for aspects of content validity, albeit with varying levels of evidence, ranging from very low to high. Five instruments showed sufficient ratings for structural validity and internal consistency, but evidence on their reliability was insufficient. No information on responsiveness was mentioned in articles. The HL19-DIGI, DHLI, eHEALS, and eHLQ were the most frequently investigated instruments.</p><p><strong>Conclusion: </strong>This review identified 17 eHL instruments, of which seven demonstrated adequate content validity. However, insufficient evidence exists regarding psychometric properties for widespread implementation. It is strongly recommended that the content of these instruments be updated to reflect patients' evolving use of eHealth services, and that further psychometrics evaluations be conducted systematically.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD42021232765.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146043799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Technology-assisted cognitive interventions are increasingly used for post-stroke cognitive impairment (PSCI), but their comparative effectiveness across modalities remains unclear.
Methods: This systematic review and network meta-analysis followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidance. The Population, Intervention, Comparator, Outcome (PICO) framework was used to define the review question. PubMed, EMBASE, Web of Science, and the Cochrane Library were searched from inception to 26 April 2025 for randomized controlled trials (RCTs) in adults with PSCI. Global cognition was assessed using the Montreal Cognitive Assessment (MoCA) and/or the Mini-Mental State Examination (MMSE). We estimated mean differences (MDs) with 95% confidence intervals (CIs) and ranked interventions using the surface under the cumulative ranking curve (SUCRA). Risk of bias was assessed using Risk of Bias 2 (RoB 2).
Results: Fourteen trials (673 participants) were included. For MoCA (9 trials; 535 participants), basic treatment plus conventional cognitive training (CT) plus virtual reality (VR) improved MoCA compared with basic treatment alone (MD = 5.70; 95% CI: 0.12 to 11.27). SUCRA suggested that basic treatment plus computerized cognitive training (CCT) plus repetitive transcranial magnetic stimulation (rTMS) ranked highest for MoCA (84.1%), followed by basic treatment plus conventional CT plus VR (74.8%). For MMSE (8 trials; 265 participants), basic treatment plus rTMS was superior to basic treatment alone (MD = 4.60; 95% CI: 0.45 to 8.75), and basic treatment plus exergaming was also superior to basic treatment alone (MD = 1.47; 95% CI: 0.04 to 2.90). SUCRA ranked basic treatment plus rTMS highest for MMSE (96.3%), followed by basic treatment plus exergaming (76.3%).
Conclusions: Technology-assisted cognitive interventions added to basic treatment may improve global cognitive function after stroke, although the current evidence remains preliminary and varies across modalities. Larger, rigorously designed RCTs are needed to confirm comparative effectiveness and guide optimal implementation in post-stroke rehabilitation.
{"title":"Effectiveness of technology-assisted cognitive interventions for post-stroke cognitive impairment: a systematic review and meta-analysis.","authors":"Ying Wang, Hui Liu, Jin-Ying Zhao, Xia Yuan, Wan-Qi Zhang, Yu-Wei Guo, Fu-Chun Wang, Bing Yan","doi":"10.1186/s13643-026-03076-2","DOIUrl":"https://doi.org/10.1186/s13643-026-03076-2","url":null,"abstract":"<p><strong>Background: </strong>Technology-assisted cognitive interventions are increasingly used for post-stroke cognitive impairment (PSCI), but their comparative effectiveness across modalities remains unclear.</p><p><strong>Methods: </strong>This systematic review and network meta-analysis followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidance. The Population, Intervention, Comparator, Outcome (PICO) framework was used to define the review question. PubMed, EMBASE, Web of Science, and the Cochrane Library were searched from inception to 26 April 2025 for randomized controlled trials (RCTs) in adults with PSCI. Global cognition was assessed using the Montreal Cognitive Assessment (MoCA) and/or the Mini-Mental State Examination (MMSE). We estimated mean differences (MDs) with 95% confidence intervals (CIs) and ranked interventions using the surface under the cumulative ranking curve (SUCRA). Risk of bias was assessed using Risk of Bias 2 (RoB 2).</p><p><strong>Results: </strong>Fourteen trials (673 participants) were included. For MoCA (9 trials; 535 participants), basic treatment plus conventional cognitive training (CT) plus virtual reality (VR) improved MoCA compared with basic treatment alone (MD = 5.70; 95% CI: 0.12 to 11.27). SUCRA suggested that basic treatment plus computerized cognitive training (CCT) plus repetitive transcranial magnetic stimulation (rTMS) ranked highest for MoCA (84.1%), followed by basic treatment plus conventional CT plus VR (74.8%). For MMSE (8 trials; 265 participants), basic treatment plus rTMS was superior to basic treatment alone (MD = 4.60; 95% CI: 0.45 to 8.75), and basic treatment plus exergaming was also superior to basic treatment alone (MD = 1.47; 95% CI: 0.04 to 2.90). SUCRA ranked basic treatment plus rTMS highest for MMSE (96.3%), followed by basic treatment plus exergaming (76.3%).</p><p><strong>Conclusions: </strong>Technology-assisted cognitive interventions added to basic treatment may improve global cognitive function after stroke, although the current evidence remains preliminary and varies across modalities. Larger, rigorously designed RCTs are needed to confirm comparative effectiveness and guide optimal implementation in post-stroke rehabilitation.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD420251066176.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146041788","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-22DOI: 10.1186/s13643-026-03073-5
Augusto Cezar Rodrigues Rocha, Matias Noll, Carlos Alexandre Vieira, Filipe Manuel Clemente, Marcelo Couto Jorge Rodrigues, José Carlos Pontes Corrêa, Claudio Andre Barbosa de Lira, Katja Weiss, Thomas Rosemann, Beat Knechte, Mário Hebling Campos, Alberto Souza Sá Filho, Gustavo De Conti Teixeira Costa
Background: Mental disorders, particularly anxiety and mood disorders, significantly impair individuals' ability to perform daily activities, potentially leading to sedentary behavior and increasing the risk of non-communicable diseases such as diabetes, cancer, and obesity. Physical activity plays a crucial role in supporting mental health, and team sports represent a promising intervention strategy. Therefore, the aim of this systematic review is to evaluate the impact of team sports practice on anxiety and mood disorders. Furthermore, it will analyze how different modalities of team sports contribute to mental health improvements and identify gaps in the current literature to guide future research directions.
Methods: This systematic review will be reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) guidelines and is registered in PROSPERO (CRD420251121611). A comprehensive search will be carried out across four electronic databases (PubMed, Embase, Web of Science, and Scopus) with no restrictions on language or publication date. Two independent reviewers will screen titles and abstracts using predefined eligibility criteria and extract data with standardized tables. A third independent reviewer will resolve any disagreements. Extracted data will include publication title, authors, year, assessment tools for anxiety and mood disorders, type of intervention, and primary outcomes related to the effects of team sports on these disorders. Risk of bias will be assessed using the Cochrane Risk of Bias tool (RoB 2.0). Data will be synthesized using a random-effects meta-analysis (DerSimonian-Laird) when at least two sufficiently homogeneous studies report the same outcome. Continuous outcomes will be pooled as mean differences (same scale) or standardized mean differences (different instruments). Statistical heterogeneity will be assessed using Cochran's Q and the I2 statistic. If heterogeneity is high (I2 > 75%) or if pooling is not feasible, findings will be summarized narratively, with planned subgroup and sensitivity analyses. The certainty of evidence will be assessed using GRADE.
Discussion: This systematic review is expected to provide comprehensive evidence on the potential effects of team sports participation on anxiety and mood disorders. By synthesizing findings from randomized controlled trial, the review aims to clarify the extent to which engaging in team sports may contribute to mental health promotion and symptom reduction. The results may inform clinical practice, guide the design of community-based interventions, and support policymakers in developing evidence-based strategies that use team sports as a non-pharmacological approach to improve psychological well-being.
背景:精神障碍,特别是焦虑和情绪障碍,严重损害个人进行日常活动的能力,可能导致久坐行为,增加患糖尿病、癌症和肥胖等非传染性疾病的风险。身体活动在支持心理健康方面起着至关重要的作用,团队运动是一种有希望的干预策略。因此,本系统回顾的目的是评估团队运动练习对焦虑和情绪障碍的影响。此外,本文将分析团队运动的不同模式对心理健康改善的贡献,并找出现有文献中的空白,以指导未来的研究方向。方法:本系统评价将按照系统评价和荟萃分析方案的首选报告项目(PRISMA-P)指南进行报告,并在PROSPERO注册(CRD420251121611)。在四个电子数据库(PubMed、Embase、Web of Science和Scopus)上进行全面检索,不受语言和出版日期的限制。两名独立审稿人将使用预定义的资格标准筛选标题和摘要,并使用标准化表格提取数据。第三位独立审查员将解决任何分歧。提取的数据将包括出版物标题、作者、年份、焦虑和情绪障碍的评估工具、干预类型以及与团队运动对这些障碍的影响相关的主要结果。将使用Cochrane风险偏倚工具(RoB 2.0)评估偏倚风险。当至少有两个充分同质的研究报告相同的结果时,将使用随机效应荟萃分析(dersimonan - laird)综合数据。连续结果将汇总为平均差异(相同量表)或标准化平均差异(不同工具)。采用Cochran’s Q和I2统计量评估统计异质性。如果异质性高(2 ~ 75%)或合并不可行,将对结果进行叙述总结,并计划进行亚组和敏感性分析。证据的确定性将使用GRADE进行评估。讨论:本系统综述旨在为团队运动参与对焦虑和情绪障碍的潜在影响提供全面的证据。通过综合随机对照试验的结果,本综述旨在阐明参与团队运动可能有助于促进心理健康和减轻症状的程度。研究结果可以为临床实践提供信息,指导社区干预措施的设计,并支持决策者制定基于证据的策略,将团队运动作为一种非药物方法来改善心理健康。试验注册:系统评价注册:PROSPERO CRD420251121611。
{"title":"Do team sports have positive effects on anxiety levels and mood disorders? A systematic review protocol.","authors":"Augusto Cezar Rodrigues Rocha, Matias Noll, Carlos Alexandre Vieira, Filipe Manuel Clemente, Marcelo Couto Jorge Rodrigues, José Carlos Pontes Corrêa, Claudio Andre Barbosa de Lira, Katja Weiss, Thomas Rosemann, Beat Knechte, Mário Hebling Campos, Alberto Souza Sá Filho, Gustavo De Conti Teixeira Costa","doi":"10.1186/s13643-026-03073-5","DOIUrl":"https://doi.org/10.1186/s13643-026-03073-5","url":null,"abstract":"<p><strong>Background: </strong>Mental disorders, particularly anxiety and mood disorders, significantly impair individuals' ability to perform daily activities, potentially leading to sedentary behavior and increasing the risk of non-communicable diseases such as diabetes, cancer, and obesity. Physical activity plays a crucial role in supporting mental health, and team sports represent a promising intervention strategy. Therefore, the aim of this systematic review is to evaluate the impact of team sports practice on anxiety and mood disorders. Furthermore, it will analyze how different modalities of team sports contribute to mental health improvements and identify gaps in the current literature to guide future research directions.</p><p><strong>Methods: </strong>This systematic review will be reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) guidelines and is registered in PROSPERO (CRD420251121611). A comprehensive search will be carried out across four electronic databases (PubMed, Embase, Web of Science, and Scopus) with no restrictions on language or publication date. Two independent reviewers will screen titles and abstracts using predefined eligibility criteria and extract data with standardized tables. A third independent reviewer will resolve any disagreements. Extracted data will include publication title, authors, year, assessment tools for anxiety and mood disorders, type of intervention, and primary outcomes related to the effects of team sports on these disorders. Risk of bias will be assessed using the Cochrane Risk of Bias tool (RoB 2.0). Data will be synthesized using a random-effects meta-analysis (DerSimonian-Laird) when at least two sufficiently homogeneous studies report the same outcome. Continuous outcomes will be pooled as mean differences (same scale) or standardized mean differences (different instruments). Statistical heterogeneity will be assessed using Cochran's Q and the I<sup>2</sup> statistic. If heterogeneity is high (I<sup>2</sup> > 75%) or if pooling is not feasible, findings will be summarized narratively, with planned subgroup and sensitivity analyses. The certainty of evidence will be assessed using GRADE.</p><p><strong>Discussion: </strong>This systematic review is expected to provide comprehensive evidence on the potential effects of team sports participation on anxiety and mood disorders. By synthesizing findings from randomized controlled trial, the review aims to clarify the extent to which engaging in team sports may contribute to mental health promotion and symptom reduction. The results may inform clinical practice, guide the design of community-based interventions, and support policymakers in developing evidence-based strategies that use team sports as a non-pharmacological approach to improve psychological well-being.</p><p><strong>Trial registrations: </strong>Systematic review registration: PROSPERO CRD420251121611.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146030898","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background and aims: Intestinal parasitic infections (IPIs) remain a significant public health challenge, particularly among school-aged children in low- and middle-income countries (LMICs). This systematic review and meta-analysis aimed to estimate the pooled prevalence of IPIs and identify associated risk factors in Africa and Asia.
Method: A systematic search of Medline/PubMed, Embase, Scopus, ScienceDirect, Epistemonikos, and additional searches such as Google and Google Scholar was conducted between January 2019 and April 2024. The review followed the PRISMA guidelines. Data extraction was performed using Microsoft Excel, and meta-analyses were conducted using STATA. Methodological quality was assessed using the Newcastle-Ottawa Scale. A random-effects model was used to estimate the pooled prevalence, while heterogeneity was assessed using the I2 statistic. Publication bias was evaluated through funnel plots and Egger's regression test. The study protocol was registered in PROSPERO (CRD42024536604).
Results: 47 studies comprising 20,334 school-aged children were included. The pooled prevalence of at least one intestinal parasitic infection was 39% (95% CI: 33%-45%). Regional analysis showed a higher prevalence in Africa (41%) compared to Asia (35%). Protozoan infections (29%) exceeded those of helminths (19%) and mixed infections (2%). The most common parasites were Blastocystis hominis (16%), Endolimax nana (16%), Entamoeba histolytica (15%), Entamoeba coli (12%), and Ascaris lumbricoides (11%). Infections were primarily single (37%), followed by double (10%), triple (3%), and quadruple (1%). Significant risk factors included school type, socioeconomic status, larger family size, presence of domestic animals, and finger-sucking habits.
Conclusion: Intestinal parasitic infections remain a significant public health challenge among school-aged children in Africa and Asia. The findings underscore the need for sustained, school-based health programs that integrate regular deworming, hygiene education, and targeted sanitation improvements. Strengthening surveillance and addressing behavioral and environmental risk factors are essential to reducing infection burden and promoting child health.
{"title":"Epidemiology of intestinal parasitic infections among school-aged children in low- and middle-income countries of Africa and Asia: a systematic review and meta-analysis.","authors":"Gelila Yitageasu, Tigist Kifle Tsegaw, Eyob Akalewold Alemu, Helen Brhan, Kassaw Chekole Adane, Fetlework Gubena Arega, Amensisa Hailu Tesfaye, Dessie Abebaw, Zemichael Gizaw, Lidetu Demoze","doi":"10.1186/s13643-025-03063-z","DOIUrl":"https://doi.org/10.1186/s13643-025-03063-z","url":null,"abstract":"<p><strong>Background and aims: </strong>Intestinal parasitic infections (IPIs) remain a significant public health challenge, particularly among school-aged children in low- and middle-income countries (LMICs). This systematic review and meta-analysis aimed to estimate the pooled prevalence of IPIs and identify associated risk factors in Africa and Asia.</p><p><strong>Method: </strong>A systematic search of Medline/PubMed, Embase, Scopus, ScienceDirect, Epistemonikos, and additional searches such as Google and Google Scholar was conducted between January 2019 and April 2024. The review followed the PRISMA guidelines. Data extraction was performed using Microsoft Excel, and meta-analyses were conducted using STATA. Methodological quality was assessed using the Newcastle-Ottawa Scale. A random-effects model was used to estimate the pooled prevalence, while heterogeneity was assessed using the I<sup>2</sup> statistic. Publication bias was evaluated through funnel plots and Egger's regression test. The study protocol was registered in PROSPERO (CRD42024536604).</p><p><strong>Results: </strong>47 studies comprising 20,334 school-aged children were included. The pooled prevalence of at least one intestinal parasitic infection was 39% (95% CI: 33%-45%). Regional analysis showed a higher prevalence in Africa (41%) compared to Asia (35%). Protozoan infections (29%) exceeded those of helminths (19%) and mixed infections (2%). The most common parasites were Blastocystis hominis (16%), Endolimax nana (16%), Entamoeba histolytica (15%), Entamoeba coli (12%), and Ascaris lumbricoides (11%). Infections were primarily single (37%), followed by double (10%), triple (3%), and quadruple (1%). Significant risk factors included school type, socioeconomic status, larger family size, presence of domestic animals, and finger-sucking habits.</p><p><strong>Conclusion: </strong>Intestinal parasitic infections remain a significant public health challenge among school-aged children in Africa and Asia. The findings underscore the need for sustained, school-based health programs that integrate regular deworming, hygiene education, and targeted sanitation improvements. Strengthening surveillance and addressing behavioral and environmental risk factors are essential to reducing infection burden and promoting child health.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146012588","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1186/s13643-025-03062-0
Patrick Kaonga, Adam Silumbwe, Isaac Fwemba, Tanyaradzwa Mabwe, Alice Ngoma-Hazemba
Background: Differentiated Service Delivery (DSD) models for HIV are antiretroviral therapy (ART) mechanisms for stable people living with HIV (PLHIV) and are meant to be patient-centered to achieve treatment goals. One key element to achieve treatment goals is clients' satisfaction with DSD models. Despite extensive implementation and scale-up of DSD models in sub-Saharan Africa, satisfaction levels remain unclear. Thus far, no comprehensive systematic review and meta-analysis regarding clients' satisfaction level with DSD models and associated factors has been published. Therefore, we aim to conduct a systematic review and meta-analysis (1) to establish the level of clients' satisfaction with DSD models, (2) to determine which specific DSD models clients are most likely to be satisfied with, and (3) to identify factors associated with clients' satisfaction with DSD models.
Methods: All eligible studies reporting empirical evidence will be identified using a predetermined search strategy in several electronic databases such as EMBASE, PubMed, Scopus, Web of Science, CINAHL, and ProQuest. Observational studies that have been conducted in sub-Saharan African countries regardless of the year of publication will be included in the systematic review and meta-analysis. We will conduct this review and meta-analysis according to the guidelines by Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA). A random effects model will be used to conduct the meta-analysis using Stata 19.5 software. Heterogeneity will be assessed by using Cochran's Q test and the I2 statistic. Bias will be evaluated using Egger's and Begg's tests as well as visually by funnel plot.
Discussion: To the best of our knowledge, this review and meta-analysis will be the first to be conducted in the sub-Saharan Africa region to synthesize empirical evidence regarding clients' satisfaction with DSD models and associated factors, as well as identify common DSD models most clients are likely to be satisfied with. Collection of existing evidence will improve and guide implementation, scale-up, and adoption of different DSD models. Such knowledge can inform program managers and implementers which DSD models are likely to result in desired HIV treatment outcomes.
背景:艾滋病毒差异化服务提供(DSD)模式是针对稳定型艾滋病毒感染者(PLHIV)的抗逆转录病毒治疗(ART)机制,旨在以患者为中心实现治疗目标。实现治疗目标的一个关键因素是客户对DSD模型的满意度。尽管在撒哈拉以南非洲广泛实施和扩大了DSD模式,但满意度仍不清楚。到目前为止,还没有关于客户对DSD模型及其相关因素满意度的综合系统评价和元分析。因此,我们的目标是进行系统回顾和荟萃分析(1)建立客户对DSD模型的满意度水平,(2)确定客户最可能满意的具体DSD模型,以及(3)确定客户对DSD模型满意度的相关因素。方法:所有符合条件的报告经验证据的研究将使用预定的搜索策略在几个电子数据库(如EMBASE, PubMed, Scopus, Web of Science, CINAHL和ProQuest)中识别。无论发表年份如何,在撒哈拉以南非洲国家进行的观察性研究将被纳入系统评价和荟萃分析。我们将根据系统评价和荟萃分析首选报告项目(PRISMA)的指南进行本综述和荟萃分析。采用随机效应模型,采用Stata 19.5软件进行meta分析。异质性将通过Cochran’s Q检验和I2统计量进行评估。偏差将使用Egger's和Begg's检验以及通过漏斗图进行视觉评估。讨论:据我们所知,这篇综述和荟萃分析将是撒哈拉以南非洲地区首次进行的综述和荟萃分析,旨在综合有关客户对DSD模型和相关因素满意度的经验证据,并确定大多数客户可能满意的常见DSD模型。收集现有证据将改进和指导实施、扩大和采用不同的DSD模型。这些知识可以告知项目经理和执行者,哪些DSD模型可能会产生预期的艾滋病毒治疗结果。系统评价注册:PROSPERO CRD420251085833。
{"title":"Clients' satisfaction with HIV differentiated service delivery models and associated factors in sub-Saharan Africa: a protocol for a systematic review and meta-analysis.","authors":"Patrick Kaonga, Adam Silumbwe, Isaac Fwemba, Tanyaradzwa Mabwe, Alice Ngoma-Hazemba","doi":"10.1186/s13643-025-03062-0","DOIUrl":"https://doi.org/10.1186/s13643-025-03062-0","url":null,"abstract":"<p><strong>Background: </strong>Differentiated Service Delivery (DSD) models for HIV are antiretroviral therapy (ART) mechanisms for stable people living with HIV (PLHIV) and are meant to be patient-centered to achieve treatment goals. One key element to achieve treatment goals is clients' satisfaction with DSD models. Despite extensive implementation and scale-up of DSD models in sub-Saharan Africa, satisfaction levels remain unclear. Thus far, no comprehensive systematic review and meta-analysis regarding clients' satisfaction level with DSD models and associated factors has been published. Therefore, we aim to conduct a systematic review and meta-analysis (1) to establish the level of clients' satisfaction with DSD models, (2) to determine which specific DSD models clients are most likely to be satisfied with, and (3) to identify factors associated with clients' satisfaction with DSD models.</p><p><strong>Methods: </strong>All eligible studies reporting empirical evidence will be identified using a predetermined search strategy in several electronic databases such as EMBASE, PubMed, Scopus, Web of Science, CINAHL, and ProQuest. Observational studies that have been conducted in sub-Saharan African countries regardless of the year of publication will be included in the systematic review and meta-analysis. We will conduct this review and meta-analysis according to the guidelines by Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA). A random effects model will be used to conduct the meta-analysis using Stata 19.5 software. Heterogeneity will be assessed by using Cochran's Q test and the I<sup>2</sup> statistic. Bias will be evaluated using Egger's and Begg's tests as well as visually by funnel plot.</p><p><strong>Discussion: </strong>To the best of our knowledge, this review and meta-analysis will be the first to be conducted in the sub-Saharan Africa region to synthesize empirical evidence regarding clients' satisfaction with DSD models and associated factors, as well as identify common DSD models most clients are likely to be satisfied with. Collection of existing evidence will improve and guide implementation, scale-up, and adoption of different DSD models. Such knowledge can inform program managers and implementers which DSD models are likely to result in desired HIV treatment outcomes.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD420251085833.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146019663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-21DOI: 10.1186/s13643-026-03071-7
Shi-Ping Sun, Chen Chen, Han Min
Background: Metabolic dysfunction-associated steatohepatitis (MASH) represents a progressive form of liver disease with rising global prevalence, where sustained weight loss is essential for histological improvement. Current therapies-lifestyle modification, pharmacotherapy, and bariatric surgery-face limitations including variable efficacy, cost, invasiveness, or accessibility. Endoscopic sleeve gastroplasty (ESG) emerges as a minimally invasive alternative for moderate obesity, demonstrating promising weight loss and preliminary metabolic benefits. However, robust evidence regarding its impact on core histological outcomes remains limited and heterogeneous, necessitating a systematic evaluation to establish its therapeutic role in MASH management.
Methods and analysis: Randomized controlled trials (RCTs) and cohort studies that compare endoscopic sleeve gastroplasty and usual care in patients with metabolic dysfunction-associated steatohepatitis will be included. Literature searches will be conducted in PubMed, Web of Science, Embase, and Cochrane Library. Two reviewers will independently perform the processes of literature retrieval, screening, data extraction, and assessment of risk of bias. The primary outcome is total body weight loss (TBWL). Secondary outcomes include resolution of MASH without worsening of fibrosis, improvement in fibrosis without worsening of steatohepatitis, and incidence of adverse events. Risk of bias in included RCTs will be evaluated using Revised Cochrane risk-of-bias tool (ROB 2) for RCTs. Review Manager (RevMan) will be used for data pooling. Effect estimates will be expressed as risk ratios (RR) for dichotomous outcomes and mean differences (MD) for continuous outcomes, with 95% confidence intervals (CI). Subgroup analysis, trial sequential analysis (TSA), and sensitivity analysis will be conducted.
Ethics and dissemination: Ethical approval is not required because this study is a secondary analysis of existing data. We will disseminate the findings through peer- reviewed publications.
背景:代谢功能障碍相关脂肪性肝炎(MASH)是一种全球患病率不断上升的进行性肝病,持续减肥对组织学改善至关重要。目前的治疗方法-生活方式改变,药物治疗和减肥手术-面临着包括不同疗效,成本,侵入性或可及性在内的局限性。内镜下套管胃成形术(ESG)作为一种微创治疗中度肥胖的替代方法,显示出有希望的减肥和初步的代谢益处。然而,关于其对核心组织学结果影响的有力证据仍然有限且异质性,需要系统评估以确定其在MASH管理中的治疗作用。方法和分析:随机对照试验(rct)和队列研究将比较内镜下胃套筒成形术和常规护理对代谢功能障碍相关脂肪性肝炎患者的影响。文献检索将在PubMed、Web of Science、Embase和Cochrane Library进行。两名审稿人将独立完成文献检索、筛选、数据提取和偏倚风险评估的过程。主要结果是总体重减轻(TBWL)。次要结局包括无纤维化恶化的MASH消退、无脂肪性肝炎恶化的纤维化改善和不良事件发生率。纳入的随机对照试验的偏倚风险将使用修订后的Cochrane随机对照试验风险偏倚工具(ROB 2)进行评估。Review Manager (RevMan)将用于数据池。效果估计将表示为二分类结果的风险比(RR)和连续结果的平均差异(MD),具有95%的置信区间(CI)。进行亚组分析、试验序贯分析(TSA)和敏感性分析。伦理和传播:由于本研究是对现有数据的二次分析,因此不需要伦理批准。我们将通过同行评议的出版物传播研究结果。系统评价注册:PROSPERO CRD420251121461。
{"title":"Efficacy and safety of endoscopic sleeve gastroplasty for patients with metabolic dysfunction-associated steatohepatitis: protocol for a systematic review and trial sequential meta-analysis.","authors":"Shi-Ping Sun, Chen Chen, Han Min","doi":"10.1186/s13643-026-03071-7","DOIUrl":"https://doi.org/10.1186/s13643-026-03071-7","url":null,"abstract":"<p><strong>Background: </strong>Metabolic dysfunction-associated steatohepatitis (MASH) represents a progressive form of liver disease with rising global prevalence, where sustained weight loss is essential for histological improvement. Current therapies-lifestyle modification, pharmacotherapy, and bariatric surgery-face limitations including variable efficacy, cost, invasiveness, or accessibility. Endoscopic sleeve gastroplasty (ESG) emerges as a minimally invasive alternative for moderate obesity, demonstrating promising weight loss and preliminary metabolic benefits. However, robust evidence regarding its impact on core histological outcomes remains limited and heterogeneous, necessitating a systematic evaluation to establish its therapeutic role in MASH management.</p><p><strong>Methods and analysis: </strong>Randomized controlled trials (RCTs) and cohort studies that compare endoscopic sleeve gastroplasty and usual care in patients with metabolic dysfunction-associated steatohepatitis will be included. Literature searches will be conducted in PubMed, Web of Science, Embase, and Cochrane Library. Two reviewers will independently perform the processes of literature retrieval, screening, data extraction, and assessment of risk of bias. The primary outcome is total body weight loss (TBWL). Secondary outcomes include resolution of MASH without worsening of fibrosis, improvement in fibrosis without worsening of steatohepatitis, and incidence of adverse events. Risk of bias in included RCTs will be evaluated using Revised Cochrane risk-of-bias tool (ROB 2) for RCTs. Review Manager (RevMan) will be used for data pooling. Effect estimates will be expressed as risk ratios (RR) for dichotomous outcomes and mean differences (MD) for continuous outcomes, with 95% confidence intervals (CI). Subgroup analysis, trial sequential analysis (TSA), and sensitivity analysis will be conducted.</p><p><strong>Ethics and dissemination: </strong>Ethical approval is not required because this study is a secondary analysis of existing data. We will disseminate the findings through peer- reviewed publications.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD420251121461.</p>","PeriodicalId":22162,"journal":{"name":"Systematic Reviews","volume":" ","pages":""},"PeriodicalIF":3.9,"publicationDate":"2026-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146019651","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}