Feasibility of cardiac rehabilitation in patients who have undergone stent insertion

Feasibility of implementing a cardiac rehabilitation algorithm in patients following percutaneous coronary intervention

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/07/014713

Enrollment

Registered

2018-07-03

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: null- patients with myocardial infarction who have undergone percutaneous coronary intervention Health Condition 2: I229- Subsequent ST elevation (STEMI) myocardial infarction of unspecified site

Interventions

Intervention1: CARDIAC REHABILITATION: phase I includes patient tolerated exercise comprising of breathing exercise, active movements of upper limb and lower limb, walking and stair climbing. All the

Eligibility

Inclusion criteria

Inclusion criteria: patients who have undergone percutaneous coronary intervention (PCI)

Exclusion criteria

Exclusion criteria: NYHA class IV Haemodynamically unstable Unstable angina Uncompensated heart failure Significant aortic stenosis Orthostatic hypotension Active pericarditis and myocarditis Uncontrolled arrythmias Acute pulmonary embolism Ejection fraction less than 20% Hypertrophic cardiomyopathy Recent stroke or transient ischemic attack (TIA) Palpitation, lethargy and dizziness Severe psychological disturbances

Design outcomes

Primary

Measure	Time frame
Feasibility metrics: 1. Process metrics-Refusal rates, referral rates and recruitment rates 2. Resource metrics-time of treatment, adherence rate, dropout rate, length of hospital stay 3. Management metrics-Adverse effects and clinical emergencies 4. Scientific metrics-response of the study (clinical measures, six-minute walk test, TAMPA heart of kinesophobia, cardiac depression scale, cardiac self-efficacy scale, WHOQOL-BREF)Timepoint: Feasibility metrics: 1. Process metrics- at the beginning and end of the study 2. Resource metrics-at the start and end of the study 3. Management metrics- at the end of the study 4. Scientific metrics-at the start of the study, on the day of discharge and at the end of the study	—

Measure

Time frame

Feasibility metrics: 1. Process metrics-Refusal rates, referral rates and recruitment rates 2. Resource metrics-time of treatment, adherence rate, dropout rate, length of hospital stay 3. Management metrics-Adverse effects and clinical emergencies 4. Scientific metrics-response of the study (clinical measures, six-minute walk test, TAMPA heart of kinesophobia, cardiac depression scale, cardiac self-efficacy scale, WHOQOL-BREF)Timepoint: Feasibility metrics: 1. Process metrics- at the beginning and end of the study 2. Resource metrics-at the start and end of the study 3. Management metrics- at the end of the study 4. Scientific metrics-at the start of the study, on the day of discharge and at the end of the study

—

Secondary

Measure	Time frame
six minute walk test, cardiac depression scale, cardiac self-efficacy scale, TAMPA scale of Kinesophobia Heart, WHOQOL-BREF questionnairresTimepoint: on the day of discharge and the end of the study (after 30 days)	—

Countries

India

Contacts

Public ContactAkhila Satyamurthy

Dept of Physiotherapy, SOAHS, MAHE

nivedita.kamath83@gmail.com8105523279

Outcome results

None listed

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