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临床试验/NCT05370703
NCT05370703已完成不适用

A Prospective, Randomized, Open-label, Clinical Study to Evaluate the Effect of Mobile Applications "My A:Care" and "Smart Coach" on the Lipid-lowering Treatment Adherence of Subjects With Dyslipidemia in Thailand

Abbott1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2022年4月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Abbott
入组人数
150
试验地点
1
主要终点
Impact of mobile applications (My A:Care and Smart Coach) on adherence to the lipid-lowering therapy in subjects with dyslipidemia using MARS-5VA questionnaire

研究概览

简要总结

A prospective, randomized, open-label, clinical study to evaluate the effect of mobile applications "My A:Care" and "Smart Coach" on the lipid-lowering treatment adherence of subjects with dyslipidemia in Thailand

详细描述

This is a prospective, randomized, open-label, clinical study in subjects with dyslipidemia and suboptimal adherence to their current lipid-lowering therapy in Thailand. Suboptimal adherence is defined as having <22 points score on the Part 1 of MARS-5VA questionnaire. This questionnaire comprises 2 parts, Medication Adherence Report Scale (MARS-5) as Part 1 and two Visual Analogue Scales (VAS) as Part 2. The complete MARS-5VA questionnaire (Part 1 and 2) will be used to evaluate subject adherence to lipid-lowering therapy in the study. The Part 1 of MARS-5VA will also be used to confirm subject's eligibility at screening. Subjects who are continuing the stable lipid-lowering therapy for at least 1 month are being considered for this study. Subjects will be randomized to different types of behavior interventions using mobile applications that will be used in addition to their current standard of care (SOC) lipid-lowering therapy.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female subjects aged 18-75 years (inclusive)
  • Subjects who have provided written informed consent
  • Subjects who were diagnosed with dyslipidemia and initiated lipid-lowering therapy based on local treatment guidelines, between 9 months and 1 month prior to the screening visit
  • Subjects who were on a stable lipid-lowering therapy within 1 month prior to the screening visit
  • Subjects who are not compliant with the prescribed lipid-lowering therapy, assessed as having <22 points score on the Part 1 of MARS-5VA questionnaire at the screening visit
  • Subjects for whom lipid profile laboratory data is available from routine care within 14 days prior to the screening visit
  • Subject must have their own Android operating system smart phone and a data package suitable for the installation and running of the mobile application and sending and receiving data
  • Willing and able to operate the mobile devices, including use of all study-related smartphone applications; able to proof regular use of mobile applications in their daily life.
  • Able to read and understand Thai
  • Willing and able to comply with the study requirements.

排除标准

  • Subjects who are diagnosed with myocardial infarction or stroke or unstable angina within 2 months prior to screening, subjects who are hospitalized for their cardio-vascular condition and requiring changes in administration of their lipid-lowering medication
  • Subjects who experienced undesirable effects of their lipid-lowering medication and who might, in the opinion of the investigator, require its modification or discontinuation during the 12 weeks of observation period of the study
  • Subjects receiving injectable lipid-lowering therapy
  • Subjects who are currently using other medication-use-related mobile applications.

结局指标

主要结局

Impact of mobile applications (My A:Care and Smart Coach) on adherence to the lipid-lowering therapy in subjects with dyslipidemia using MARS-5VA questionnaire

时间窗: 12 weeks (± 7 days)

Adherence is measured by change from Baseline in MARS-5VA Scores at 12 Weeks

次要结局

  • Impact of mobile applications (My A:Care and Smart Coach) on level of lipid control in subjects with dyslipidemia by measuring the subject's lipid profile(12 weeks (± 7 days))
  • Impact of mobile applications (My A:Care and Smart Coach) on the subjects' perception to medications in general using BMQ-General-12 and PSM-5 Questionnaires(12 weeks (± 7 days))
  • Impact of mobile applications (My A:Care and Smart Coach) on the subjects' perception to medications specific to lipid-lowering therapy using BMQ-S11-Plural and MAIN Screen Questionnaires(12 weeks (± 7 days))

研究者

发起方
Abbott
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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