CTRI/2023/03/051109尚未招募Unknown
Validation and pilot testing of an android smartphone application for lifestyle modification in patients with hypertension
Google LLC0 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
- •Inclusion Criteria for Expert Group
- •1. Post-graduate degree in Internal Medicine/ Emer-gency Medicine
- •2. Five or more years experience in treating adult hypertensive patients
- •3. Working in JIPMER
- •Inclusion Criteria for Patient Group
- •1.Age > 30 years and Age < 75 years
- •2. Diagnosis of hypertension that is being treated by a physician with stable antihypertensive medication for 6 months. (No changes to BP medication regi-men for 6 months)
- •3. Not part of another ongoing study for hyperten-sion
- •4. Own an android smartphone with mobile data
- •5. Can use smartphone, smartwatch & BP machine
- •6. Fluency in English
- •7. Provide written informed consent
- •8. Participant is able to follow lifestyle changes
排除标准
- •Exclusion Criteria for Expert and patient Groups
- •1. Medical history, clinical signs or laboratory results indicating secondary hypertension, including primary aldosteronism or renal artery stenosis
- •2.Average SBP > 180mmHg in last six months or current SBP of >180mmHg or DBP >100mmHg
- •3. Unable or unwilling to measure BP or follow life-style changes
- •4. Medical conditions that limit study participation such as resistant hypertension, hypertensive urgency or emergency, Ischemic Heart Disease, Valvular Heart Disease, Pulmonary Hypertension, heart failure, peripheral arterial disease, atrial fibrillation, tachy/bradyarrhythmia on any kind of cardiac rhythm management device, aortic stenosis, severe arthritis, renal failure, visual/auditory/ cognitive/motor impairment.
- •5. Pregnancy
- •6. Inability to understand study procedures and/or the informed consent process
- •7. Other medical complications that preclude completion of the study as determined by the principal investigator.
研究者
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