跳至主要内容
临床试验/KCT0006508
KCT0006508尚未招募未知

Integrated pharmaceutical care service model using personalized mobile applications for patients with rheumatoid arthritis

Daegu Catholic University Medical Center0 个研究点目标入组 282 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
282

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
18?(Year) 至 o Limit(—)
性别
All

入选标准

  • 1) Among outpatients 18 years of age or older who visit the Department of Rheumatology at Daegu Catholic University Hospital, those who have been diagnosed with rheumatoid arthritis and have received one or more of the following DMARDs
  • - Conventional DMARDs: Hydroxychloroquine, methotrexate, sulfasalazine, bucillamine, leflunomide, tacrolimus
  • - Biologic DMARDs (subcutaneous): etanercept, adalimumab, golimumab, tocilizumab, abatacept
  • - JAK inhibitor: tofacitinib, baricitinb, upadacitinib
  • 2) Patients who started taking a new drug (DMARD, steroid, or analgesic) at the time of randomization
  • 3) Persons with mobile devices (smartphones, etc.)
  • 4) Patients who agreed to participate in the study

排除标准

  • 1) Patients who have difficulty responding to written or interview questionnaires due to cognitive impairment, etc.
  • 2) Patients with severe systemic or malignant disease
  • 3) Patients who do not agree to install the medication guide tool (an application or app developed in this study) on the mobile device
  • 4) Patients who do not agree to provide medication information using Multimedia Messaging Service (MMS)
  • 5) Patients judged by other researchers as inappropriate to participate in the study

研究者

发起方
Daegu Catholic University Medical Center

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