TY -非盟的林德Ditte年代盟——Bakiewicz Aleksandra AU - Normann,安妮·卡特琳AU -汉森,尼娜贝克盟——Lundh Andreas AU -拉希,Vibeke PY - 2020 DA - 2020/12/11 TI -亲密伴侣暴力和电子卫生干预措施:系统回顾和荟萃分析的随机试验乔- J地中海互联网Res SP - e22361六世- 22 - 12 KW -电子健康KW -随机试验KW -亲密伴侣暴力KW -家庭暴力千瓦滥用KW -抑郁KW - PTSD AB -背景:亲密伴侣暴力(IPV)是一个重大的公共卫生问题。电子保健干预措施可减少遭受暴力和健康相关后果的风险，因为该技术为目标人群提供了安全和灵活的空间。然而，证据尚不明确。目的:本综述的目的是研究与标准护理相比，电子健康干预在降低暴露于IPV的妇女的IPV、抑郁和创伤后应激障碍(PTSD)方面的效果。方法:我们检索了EMBASE、MEDLINE、Cochrane对照试验中央登记册、PsycInfo、Scopus、全球健康图书馆、ClinicalTrials.gov和国际临床试验注册平台，以检索从创建到2019年4月已发表和未发表的试验。其中包括针对遭受暴力的妇女的电子健康干预试验。我们使用Cochrane偏倚风险工具评估偏倚风险。报告总体IPV效应估计的试验;身体、性和心理暴力; depression; or posttraumatic stress disorder were included in meta-analyses. Results: A total of 14 trials were included in the review; 8 published trials, 3 unpublished trials and 3 ongoing trials. Of the 8 published trials, 2 were judged as overall low risk of bias trials. The trials reported 23 types of outcomes, and 7 of the trials had outcomes that were eligible for meta-analyses. Our pooled analyses found no effect of eHealth interventions on any of our prespecified outcomes: overall IPV (SMD –0.01; 95% CI –0.11 to 0.08; I2=0%; 5 trials, 1668 women); physical violence (SMD 0.01; 95% CI –0.22 to 0.24; I2=58%; 4 trials, 1128 women); psychological violence (SMD 0.07; 95% CI –0.12 to 0.25; I2=40%; 4 trials, 1129 women); sexual violence (MD 0.36; 95% CI –0.18 to 0.91; I2=0%; 2 trials, 1029 women); depression (SMD –0.13; 95% CI –0.37 to 0.11; I2=78%; 5 trials, 1600 women); and PTSD (MD –0.11; 95% CI –1.04 to 0.82; I2=0%; 5 trials, 1267 women). Conclusions: There is no evidence from randomized trials of a beneficial effect of eHealth interventions on IPV. More high-quality trials are needed, and we recommend harmonizing outcome reporting in IPV trials by establishing core outcome sets. Trial Registration: PROSPERO International Prospective Register of Systematic Reviews CRD42019130124; https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=130124 SN - 1438-8871 UR - //www.mybigtv.com/2020/12/e22361/ UR - https://doi.org/10.2196/22361 UR - http://www.ncbi.nlm.nih.gov/pubmed/33306030 DO - 10.2196/22361 ID - info:doi/10.2196/22361 ER -