Ignite Creation Date:
2024-05-06 @ 8:17 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06325189
Status:
COMPLETED
Last Update Posted:
2024-03-22
First Post:
2024-03-17
Brief Title:
Effects of Aerobic Interval Training on Fatigue Level and Functional Performance in Post Angioplasty Patients
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Effects of Aerobic Interval Training on Fatigue Level and Functional Performance in Post Angioplasty Patients
Status:
COMPLETED
Status Verified Date:
2024-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
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
Detailed 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
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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None