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首页> 外文期刊>JMIR Research Protocols >A Web-Based Decision Tool to Improve Contraceptive Counseling for Women With Chronic Medical Conditions: Protocol For a Mixed Methods Implementation Study
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A Web-Based Decision Tool to Improve Contraceptive Counseling for Women With Chronic Medical Conditions: Protocol For a Mixed Methods Implementation Study

机译:基于Web的决策工具,可改善患有慢性病的女性的避孕咨询:混合方法实施方案的协议

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摘要

Background Women with chronic medical conditions, such as diabetes and hypertension, have a higher risk of pregnancy-related complications compared with women without medical conditions and should be offered contraception if desired. Although evidence based guidelines for contraceptive selection in the presence of medical conditions are available via the United States Medical Eligibility Criteria (US MEC), these guidelines are underutilized. Research also supports the use of decision tools to promote shared decision making between patients and providers during contraceptive counseling. Objective The overall goal of the MiHealth, MiChoice project is to design and implement a theory-driven, Web-based tool that incorporates the US MEC (provider-level intervention) within the vehicle of a contraceptive decision tool for women with chronic medical conditions (patient-level intervention) in community-based primary care settings (practice-level intervention). This will be a 3-phase study that includes a predesign phase, a design phase, and a testing phase in a randomized controlled trial. This study protocol describes phase 1 and aim 1, which is to determine patient-, provider-, and practice-level factors that are relevant to the design and implementation of the contraceptive decision tool. Methods This is a mixed methods implementation study. To customize the delivery of the US MEC in the decision tool, we selected high-priority constructs from the Consolidated Framework for Implementation Research and the Theoretical Domains Framework to drive data collection and analysis at the practice and provider level, respectively. A conceptual model that incorporates constructs from the transtheoretical model and the health beliefs model undergirds patient-level data collection and analysis and will inform customization of the decision tool for this population. We will recruit 6 community-based primary care practices and conduct quantitative surveys and semistructured qualitative interviews with women who have chronic medical conditions, their primary care providers (PCPs), and clinic staff, as well as field observations of practice activities. Quantitative survey data will be summarized with simple descriptive statistics and relationships between participant characteristics and contraceptive recommendations (for PCPs), and current contraceptive use (for patients) will be examined using Fisher exact test. We will conduct thematic analysis of qualitative data from interviews and field observations. The integration of data will occur by comparing, contrasting, and synthesizing qualitative and quantitative findings to inform the future development and implementation of the intervention. Results We are currently enrolling practices and anticipate study completion in 15 months. Conclusions This protocol describes the first phase of a multiphase mixed methods study to develop and implement a Web-based decision tool that is customized to meet the needs of women with chronic medical conditions in primary care settings. Study findings will promote contraceptive counseling via shared decision making and reflect evidence-based guidelines for contraceptive selection. Trial Registration ClinicalTrials.gov {"type":"clinical-trial","attrs":{"text":"NCT03153644","term_id":"NCT03153644"}} NCT03153644 ; https://clinicaltrials.gov/ct2/show/ {"type":"clinical-trial","attrs":{"text":"NCT03153644","term_id":"NCT03153644"}} NCT03153644 (Archived by WebCite at http://www.webcitation.org/6yUkA5lK8).
机译:背景技术与没有医疗状况的女性相比,患有慢性医疗状况的女性(例如糖尿病和高血压)与妊娠相关并发症的风险更高,因此,如果需要,应给予避孕措施。尽管可以通过美国医疗资格标准(US MEC)获得存在医疗条件下避孕选择的循证指南,但这些指南的使用率较低。研究还支持在避孕咨询过程中使用决策工具来促进患者和提供者之间的共同决策。目标MiHealth,MiChoice项目的总体目标是设计和实施一种基于理论的基于Web的工具,该工具将US MEC(提供者级干预)纳入针对慢性病患者的避孕决策工具的工具(基于社区的初级保健环境中的患者级别干预(实践级别干预)。这将是一个分为三个阶段的研究,包括随机对照试验中的预设计阶段,设计阶段和测试阶段。该研究方案描述了阶段1和目标1,即确定与避孕决策工具的设计和实施相关的患者,提供者和实践水平的因素。方法这是一项混合方法实施研究。为了在决策工具中自定义美国MEC的交付方式,我们从实施研究合并框架和理论领域框架中选择了高度优先的结构,以分别在实践和提供者级别推动数据收集和分析。结合了跨理论模型和健康信念模型的构造的概念模型将为患者级别的数据收集和分析提供基础,并将为该人群的决策工具提供定制信息。我们将招募6种基于社区的初级保健实践,并对患有慢性病的女性,其初级保健提供者(PCP)和诊所工作人员进行定量调查和半结构化定性访谈,以及对实践活动进行现场观察。定量调查数据将通过简单的描述性统计数据进行汇总,参与者特征与避孕建议(对于PCP)之间的关系将被汇总,当前的避孕用法(对于患者)将使用Fisher精确检验进行检查。我们将通过访谈和实地观察对定性数据进行主题分析。数据的整合将通过比较,对比和综合定性和定量结果来进行,以为该干预措施的未来发展和实施提供信息。结果我们目前正在招收实习医生,预计在15个月内完成研究。结论本协议描述了多阶段混合方法研究的第一阶段,该研究旨在开发和实施基于Web的决策工具,该工具可定制以满足在初级保健机构中患有慢性病的女性的需求。研究结果将通过共同的决策促进避孕咨询,并反映基于证据的避孕选择指南。试验注册ClinicalTrials.gov {“ type”:“ clinical-trial”,“ attrs”:{“ text”:“ NCT03153644”,“ term_id”:“ NCT03153644”}}} NCT03153644; https://clinicaltrials.gov/ct2/show/ {“ type”:“ clinical-trial”,“ attrs”:{“ text”:“ NCT03153644”,“ term_id”:“ NCT03153644”}} NCT03153644(由WebCite存档在http://www.webcitation.org/6yUkA5lK8)。

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