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Effects of Aerobic Interval Training on Fatigue Level and Functional Performance in Post Angioplasty Patients

Coronary Artery Disease Clinical Trial

Official title:
Effects of Aerobic Interval Training on Fatigue Level and Functional Performance in Post Angioplasty Patients

Clinical Trial Summary

The goal of this randomized controlled trial is to determine the effects of aerobic interval training on levels of tiredness and functional performance in post-angioplasty patients. The main question it aims to answer is: Does aerobic interval training reduce fatigue and improve functional performance compared to medication alone in post-angioplasty patients? Participants will: Be randomly assigned to either the control group (medication) or the experimental group (medication + aerobic interval training) Perform aerobic interval training for 30 minutes, three times a week, for six weeks (experimental group only) Complete pre and post-intervention assessments using the fatigue severity scale, the 6-minute walk test, and the one minute sit to stand test Researchers will compare the two groups to see if aerobic interval training leads to significant improvements in fatigue levels and functional performance.

Clinical Trial Description

The study is a randomized controlled trial that aims to evaluate the effects of aerobic interval training (AIT) on fatigue level and functional performance in post-angioplasty patients. The study involves 47 participants who have undergone percutaneous coronary intervention (PCI) for coronary artery disease (CAD) and have completed phase 1 of cardiac rehabilitation. The participants are divided into two groups: Group A receives medication only, and Group B receives medication plus AIT. The AIT consists of four sessions per week for four weeks, with each session lasting 40 minutes and alternating between high and low-intensity intervals. The study hypothesizes that AIT will have a positive effect on fatigue level and functional performance in post-angioplasty patients, compared to medication alone. The study uses descriptive statistics, paired t-tests, and independent t-tests to analyze the data and test the hypotheses. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06325189
Study type Interventional
Source Riphah International University
Contact
Status Completed
Phase N/A
Start date July 20, 2023
Completion date December 10, 2023
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