QuitAdvisorDDS: A Point-of-Care Tobacco Cessation Tool for Dental Settings
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 248
- 试验地点
- 2
- 主要终点
- Primary Patient Feasibility A: Rate of Patient Completion of 1-Month Follow-Up Survey
研究概览
简要总结
Using a single-arm trial design, this study will examine the feasibility and acceptability of evaluating QuitAdvisorDDS, a clinical decision support software application designed to facilitate implementation of evidence-based tobacco treatment interventions into the dental setting. The study will examine the feasibility and acceptability of evaluating the impact of the QuitAdvisorDDS tool on patient outcomes related to tobacco use and cessation attempts as well as provider knowledge, attitudes, and practices regarding tobacco treatment. Practitioners (dentists and hygienists) will complete surveys at baseline and follow-up, while patients will complete surveys at baseline and 1-month follow-up. An embedded substudy will also evaluate the feasibility and acceptability of collecting biospecimens (saliva) to serve as biochemical verification of smoking status.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Receives dental care from a participating practitioner;
- •Is age 18 or older;
- •Self-reports tobacco use within the past month;
- •Willing to comply with all study procedures and be available for the duration of the study;
- •Willing to provide verbal informed consent;
- •Has access to a telephone, and agrees to receive text messages, emails, or telephone calls related to the study. (The patient's preferred method of contact will be ascertained).
- •Willing to be contacted on a regular basis by each of these entities: the practice;Regional Coordinators (RC) and/or University of Kentucky (UK) researchers; and
- •Willing to provide contact information of one person living at a different address who will know the patient's whereabouts in the event the patient cannot be reached.
排除标准
- •Psychiatric disability or mental illness judged by the practitioner to be clinically significant so as to preclude informed consent or compliance with procedures of study visits.
- •Cognitive impairment judged by the practitioner to be significant so as to preclude informed consent or compliance with procedures of study visits.
研究组 & 干预措施
QA-DDS
Patients will receive exposure to the QA-DDS tool from their dental care practitioner.
干预措施: QA-DDS (Behavioral)
结局指标
主要结局
Primary Patient Feasibility A: Rate of Patient Completion of 1-Month Follow-Up Survey
时间窗: 1-Month Follow-Up
80% of the enrolled dental care patients must complete the 1-month follow-up survey with the 7-day point prevalence measure of self-reported smoking status.
Primary Patient Acceptability A: Rate of Patient Wanting Provider to Use QA-DDS
时间窗: Immediately Post-Consultation up to 1 week
80% of participating patients must indicate that they would want their dental practitioner to continue to use QA-DDS.
Primary Patient Acceptability B: Rate of Patient Wanting to Use QA-DDS Patient Portal
时间窗: 1-Month Follow-Up
80% of participating patients must indicate that they would want to continue to use the QA-DDS Patient Portal.
次要结局
- Secondary Patient Acceptability A: Average QA-DDS Satisfaction Ratings Among Patients on 0-10 Scale(Immediately Post-Consultation up to 1 week)
- Secondary Patient Feasibility A: Rate of Patient Accrual by Study Practices(4-Month Follow-Up)
研究者
Jamie Studts
Principle investigator
University of Kentucky