Smartphone app for heart attack patients- A Clinical Trial
Not Applicable
- Conditions
- Health Condition 1: I259- Chronic ischemic heart disease, unspecified
- Registration Number
- CTRI/2021/12/038617
- Lead Sponsor
- JIPMER Alumni Association of North America
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients with clinically documented stable CAD attending cardiology OPD of JIPMER hospital.
2. 18 years to 64 years
3. Able to use a smart phone with android function
4. Able to read English or Tamil
Exclusion Criteria
1. Recent ACS or PCI within 1 month
2. Patients awaiting revascularization
3. Has visual, auditory, cognitive or motor impairment
4. LVEF <35%
5. COPD, Peripheral Vascular Disease, Post Pacemaker
6. Recent CABG within 6 months.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Medication adherence will be measured by assessing the number of adherence failure events (defined as 1 missed dose during a observation cycle of 30 days) using pill counting method and Medication adherence score. <br/ ><br> <br/ ><br>Improvement of CV risk factor targets (defined before). <br/ ><br>Timepoint: Medication adherence will be measured by assessing the number of adherence failure events (defined as 1 missed dose during a observation cycle of 30 days) using pill counting method. <br/ ><br> <br/ ><br>Improvement of CV risk factor targets (defined before). <br/ ><br>
- Secondary Outcome Measures
Name Time Method Change in Quality of Life, Stress level and Quality of sleep are the secondary outcomes measured at baseline, 12 weeks and 24 weeksTimepoint: 3