None listed
Conditions
Interventions
Medical Device : 120 patients are randomly assigned to two groups to conduct clinical trials for 6 months of intervention and 3 months of follow-up. Patients assigned to both groups should receive the
s own health information, and provided custom messages for lifestyle improvement 6 times. Control patients will be given the same treatment (standard medical therapy and “Heart Guard” application rele
Sponsors
Koera University Guro Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Of the patients who underwent coronary intervention within 1 month, 1. Those who are 18 years old or older 2. Those who can use the smartphone 3. Those who are not diagnosed with cognitive dysfunction such as stroke or dementia or psychiatric disorders such as anxiety or depression 4. Those who voluntarily agree to participate in the trial.
Exclusion criteria
Exclusion criteria: 1. Patients who did not have a smartphone. 2. Patients who have undergone surgical treatment such as coronary artery bypass surgery 3. Patients with uncontrolled arrhythmia or heart failure 4. Patients with severe chronic obstructive pulmonary disease or uncontrolled asthma 5. Patients with renal failure or on dialysis 6. Patients with terminal cancer 7. Patients who can not communicate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of cardiovascular risk factors in patients ;Improvement of patients' self-management | — |
Secondary
| Measure | Time frame |
|---|---|
| Sustainability and satisfaction in the "Ansim" application;Improvement in health-related quality of life;Economic effect and reducction in medical cost | — |
Countries
Korea, Republic of
Contacts
Public ContactJi Park Kim
Sejong General Hospital
Outcome results
None listed