Is a Smartphone Application Effective as an Oral Medication Adherence Aid
试验速览
- 阶段
- 1 期
- 状态
- 终止
- 入组人数
- 68
- 试验地点
- 3
- 主要终点
- Change from baseline in number of pills taken over number of pills prescribed at 4 weeks
研究概览
简要总结
This research will act as a pilot study that will be conducted to determine the effectiveness of a smartphone medication adherence application on adherence to oral hypertensive, diabetic, and dyslipidemic medications using a prospective randomized design. Subjects will be recruited from the University of Arkansas for Medical Sciences (UAMS) Internal Medicine Clinic North, and the study data will be collected using only subject self-reports and subject pharmacy records.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 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
- 否
入选标准
- •Males and females at least 18 years of age
- •Provide informed consent
- •Prescribed an oral medication indicated for hypertension, diabetes, or dyslipidemia during 12 weeks pre-enrollment
- •Own a smartphone (Android or iOS) with unlimited text messaging, email access, and app store access
- •Oral confirmation that the subject has not previously used a medication adherence app
- •Able to consult with a pharmacy or medical student during the recruitment process for purposes of consent, data collection, and/or medication reconciliation, and/or MyMedSchedule registration
排除标准
- •Severely impaired vision
- •Reside in a nursing home
- •Non-ambulatory/bedridden
- •Not fluent in English
研究组 & 干预措施
Standard Care
The control group will not use the medication adherence app
Medication Adherence Smartphone App
The experimental group will receive the medication adherence app on their smartphone and will have their entire outpatient medication list pushed to the application. Text message reminders will be sent to their phones at the appropriate times.
干预措施: Medication Adherence Smartphone App (Other)
结局指标
主要结局
Change from baseline in number of pills taken over number of pills prescribed at 4 weeks
时间窗: Change from baseline to 4 weeks
Change from baseline in number of pills taken over number of pills prescribed at 12 weeks
时间窗: Change from baseline to 12 weeks
次要结局
未报告次要终点