The purpose of the Effectiveness of blended care on anxiety and discomfort
Not Applicable
- Conditions
- Health Condition 1: I222- Subsequent non-ST elevation (NSTEMI) myocardial infarction
- Registration Number
- CTRI/2023/06/053530
- Lead Sponsor
- KARTHIK M V
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients who are alert and cooperative.
Patients who are hemodynamically stable.
Patients undergoing Percutaneous coronary intervention for the first time.
Patients who are willing to participate in the study.
Patients who speak either Tamil, English ,or Kannada.
Exclusion Criteria
Patient who are critically ill.
Patients who will be undergoing emergency PCI.
Patients having history of using Anxiolytic drug
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the efficacy of blended care on anxiety and discomfortTimepoint: 3 days
- Secondary Outcome Measures
Name Time Method To assess the efficacy of blended care on anxiety and discomfort with the baseline and clinical variablesTimepoint: 3 days