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性传播感染的健康信息和监测(SIM 研究):一项旨在提高梅毒治疗和随访依从性的单中心、平行、三臂随机对照试验方案。

Health Information and Monitoring of Sexually Transmitted Infections (SIM study): a single-center, parallel, three-arm randomized controlled trial protocol for enhancing adherence to syphilis treatment and follow-up.

机构信息

Hospital Moinhos de Vento, Porto Alegre, Brazil.

Graduate Program in Health Sciences and Pediatrics, Federal University of Health Sciences of Porto Alegre, Porto Alegre, Brazil.

出版信息

Trials. 2022 May 26;23(1):445. doi: 10.1186/s13063-022-06383-w.

Abstract

BACKGROUND

Syphilis has recently resurfaced as a significant public health problem. Since the 2000s, isolated syphilis outbreaks have increasingly occurred in North America, Europe, and Australia; in Brazil, there have been progressive increases in both congenital and acquired syphilis. There are several possible explanations, such as misdiagnosis of acquired syphilis, which could increase the number of untreated transmitters in the population; failure to initiate or complete treatment; and nontreatment of sexual partners (leading to reinfection). Mobile technologies have been successfully used to promote behavior changes and can positively impact treatment and follow-up adherence in patients with infectious diseases. The purpose of this clinical trial is to evaluate treatment and monitoring methods in patients with syphilis, including follow-up by telephone, via a game in a smartphone app, and at public health centers.

METHODS

The SIM study is a single-center, randomized controlled trial with a 12-month follow-up period. The aim is to identify the most effective method of follow-up regarding patient compliance with treatment. The tests will be performed in a mobile unit in easily accessible locations. The goal is to perform 10,000 rapid tests for syphilis. Patients with a confirmed diagnosis according to VDRL tests will be randomized to one of three arms: telephone, smartphone game, or conventional in-person follow-up. All analyses will follow the intention-to-treat principle.

CONCLUSION

If we find differences in effectiveness, a major change in the conventional approach for this patient population may be needed, potentially affecting current Brazilian health policy strategies.

TRIAL REGISTRATION

NTC04753125 . Version 1 of protocol 1/09/2020.

摘要

背景

梅毒最近再次成为一个重大的公共卫生问题。自 2000 年代以来,北美的孤立梅毒爆发越来越多,欧洲和澳大利亚;在巴西,先天性和后天性梅毒的发病率都在逐步上升。有几种可能的解释,例如后天性梅毒的误诊,这可能会增加人群中未经治疗的传播者数量;未能开始或完成治疗;以及未治疗性伴侣(导致再次感染)。移动技术已成功用于促进行为改变,并能对传染病患者的治疗和随访依从性产生积极影响。本临床试验的目的是评估梅毒患者的治疗和监测方法,包括通过电话、智能手机应用程序中的游戏以及公共卫生中心进行随访。

方法

SIM 研究是一项单中心、随机对照试验,随访期为 12 个月。目的是确定最有效的随访方法,以提高患者对治疗的依从性。测试将在移动单元中在易于到达的地点进行。目标是进行 10000 次梅毒快速检测。根据 VDRL 检测确诊的患者将随机分为三组:电话、智能手机游戏或常规面对面随访。所有分析都将遵循意向治疗原则。

结论

如果我们发现有效性存在差异,可能需要对这一患者群体的常规方法进行重大改变,这可能会影响当前巴西的卫生政策策略。

试验注册

NTC04753125。方案 1 的第 1 版/2020 年 9 月 1 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8f6/9137047/0c2e37b9b1b3/13063_2022_6383_Fig1_HTML.jpg

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