CTRI/2023/12/060515尚未招募Unknown
A real-world evidence study to examine the effect of individualized follow-up of Smart Phone Application (SPA) based standard of care versus standard of care among the patients with Heart Failure (HF) - HF Study
upin Digital Health0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Subjects aged more than 18 years or older
- •Subjects who have a documented diagnosis of New York Heart Association NYHA class II and class III Heart Failure
- •Patients willing to comply with the follow up plan set as per real world scenario
- •Patient should have a smartphone and should be able to operate it
- •Patient who has read the informed consent form has understood the relevant aspects of the study and grants his or her authorization to participate by signing the informed consent form before the inclusion in the study
- •Patients with basic reading skills English Hindi Marathi
排除标准
- •Patients unable to participate in self management programs or unable to operate smartphone for purposes of trial due to medical care needs vision hearing cognitive or dexterity impairment
- •Patients who do not have the experience of operating mobiles or smartphones
- •Patients with a history of psychiatric and neurological disorders
- •Patients with impaired bilateral hearing or visual impairment which limits the use of smartphones
- •Patients who are participating in other ongoing clinical trials or prospective cohort studies
- •Female patients who are pregnant or lactating
- •Patients with contraindications or severe physical disabilities that limit patients from participation
- •Patients who are not willing to provide his or her own consent for participation in this study Patients who are unsuitable for any other reason to participate in the study in the opinion of the investigator
研究者
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