Skip to content

Evaluating the Impact of a Nurse Led Follow Up Clinic on Health Outcomes of Myocardial Infarction Patients and Their Caregivers in a Hospital setting

A randomized control trial to assess the effectiveness of Nurse led Myocardial infarction follow up clinic on selected outcome variables of patients and caregivers of patients with Myocardial Infarction attending Cardiology OPD in a tertiary care hospital.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078580
Enrollment
110
Registered
2024-12-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I708- Atherosclerosis of other arteries

Interventions

Intervention1: NURSE LED MYOCARDIAL INFARCTION FOLLOW UP CLINIC: If the subject agree to participate in the study, they will be selected according to inclusion and exclusion criteria. After that, acco

Sponsors

Dainy Thomas
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients’ willingness to participate 2. Patients who can read/ understand Hindi/English 3. Patients who are hemodynamically stable at the time of recruitment. 4. MI patients attending Cardiology O.P.D, A.I.I.M.S, Nagpur 5. Patient with New York Heart Association (NYHA) classification I, and II 6. Patients diagnosed with MI and undergone angioplasty. 7. Patients residing in or near Nagpur 8. Having access to a telephone 9. Not suffering from any severe and life-threatening diseases 10.Having the ability to perform daily routine activities.

Exclusion criteria

Exclusion criteria: 1. Patients who have undergone CABG 2. Patients diagnosed with psychiatric disorders. 3. NYHA grade III or IV congestive heart failure (CHF) 4. Patients with any other chronic systemic illness like Cancer and Chronic Kidney Disease • Postoperative angina 5. Significant Left ventricular dysfunction (LVEF) less than 20 percentage 6. History of sustained VT or fibrillation 7. Incapable of self-monitoring 8. Myocardial ischemia with exercise 9. History of sustained life-threatening supraventricular arrhythmia • History of sudden cardiac arrest 10. Initial therapy of patients with automatic implantable cardioverter-defibrillator (AICD) or a rate-adaptive cardiac pacemaker 11. Not answering the telephone for more than three consecutive times

Design outcomes

Primary

MeasureTime frame
The primary outcomes will be medication adherence and adherence to CVD-related lifestyle practices, while the secondary outcomes will be patient satisfaction, changes in biophysiological (ECG, Blood pressure, Ejection fraction and heart rate) and biochemical parameters (Lipid profile, RFT, FBS, HbA1C, and CRP), burden of the caregivers of the patients, and the presence of complications.Timepoint: Time points of outcome assessment are at baseline, 4 weeks, 12 weeks and 24 weeks after angioplasty

Secondary

MeasureTime frame
The secondary outcomes will be patient satisfaction, changes in biophysiological (ECG, Blood pressure, Ejection fraction and heart rate) and biochemical parameters (Lipid profile, RFT, FBS, HbA1C, and CRP), burden of the caregivers of the patients, and the presence of complications.Timepoint: The outcomes will be assessed at baseline (before discharge), after 1 month, 3 months and 6 months after discharge.

Countries

India

Contacts

Public ContactDainy Thomas

College of Nursing All India Institute of Medical Sciences Nagpur

dainyelby@gmail.com9810785066

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026