Rationale and design of the Atrial Fibrillation health Literacy Information Technology Trial: (AF-LITT)

被引:9
作者
Guhl, Emily N. [1 ]
Schlusser, Courtney L. [2 ]
Henault, Lori E. [3 ]
Bickmore, Timothy W. [4 ]
Kimani, Everlyne [4 ]
Paasche-Orlow, Michael K. [3 ]
Magnani, Jared W. [2 ]
机构
[1] Univ Pittsburgh, Dept Med, Med Ctr, 200 Lothrop St, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, UPMC Heart & Vasc Inst, Dept Med, Div Cardiol, 200 Lothrop St, Pittsburgh, PA 15213 USA
[3] Boston Univ, Sch Med, Dept Med, Sect Gen Internal Med, 801 Massachusetts Ave, Boston, MA 02118 USA
[4] Northeastern Univ, Coll Comp & Informat Sci, 360 Huntington Ave, Boston, MA 02115 USA
关键词
Randomized clinical trial; Atrial fibrillation; Health-related quality of life; Adherence; Relational agents; ADHERENCE; SEVERITY; VALIDITY; WARFARIN; SYSTEM; RISK;
D O I
10.1016/j.cct.2017.09.005
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Atrial Fibrillation (AF) is a common cardiac arrhythmia that is challenging for patients and adversely impacts health-related quality of life (HRQoL). Long-term management of AF requires that patients adhere to complex therapies, understand difficult terminology, navigate subspecialty care, and have continued symptom monitoring with the goal of preventing adverse outcomes. Continued interventions to ameliorate the patient experience of AF are essential. Design: The Atrial Fibrillation health Literacy Information Technology Trial (AF-LITT; NCT03093558) is an investigator-initiated, 2-arm randomized clinical trial (RCT). This RCT is a pilot in order to implement a novel, smartphone-based intervention to address the patient experience of AF. This pilot RCT will compare a combination of the Embodied Conversational Agent (ECA) and the Alive Cor Kardia Mobile heart rhythm monitor to the current standard of care. The study will enroll 180 adults with non-valvular AF who are receiving anticoagulation for stroke prevention and randomize them to receive a 30-day intervention (smartphone-based ECA/Kardia) or standard of care, which will include a symptom and adherence journal. The primary end-points are improvement in HRQoL and self-reported adherence to anticoagulation. The secondary end-points are the acceptability of the intervention to participants, its use by participants, and acceptability to referring physicians. Conclusions: The AF-LITT pilot aims to evaluate the efficacy of the ECA/Kardia to improve HRQoL and anticoagulant adherence, and to guide its implementation in a larger, multicenter clinical trial. The intervention has potential to improve HRQoL, adherence, and health care utilization in individuals with chronic AF.
引用
收藏
页码:153 / 158
页数:6
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