The Effect of Different Exercise Programs in Coronary Artery Patients: A Randomized Controlled Study

Exercise Clinical Trial

Official title:

The Effect of Different Exercise Programs in Coronary Artery Patients: A Randomized Controlled Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04048057
• Other study ID #: KMSU-Exercise
• Status: Completed
• Phase: N/A
• Start date: July 15, 2019
• Est. completion date: January 1, 2022

Study information

• Verified date: August 2022
• Source: Kutahya Health Sciences University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There are studies showing the superiority of HIIT protocols in patients with CAD in the literature, however there is no consensus on the use of HIIT protocols in CAD patients. In addition, in these studies, the HIIT protocols differ in severity and duration and there is no optimal HIIT protocol. Therefore, this study was planed to investigate of two different HIIT protocols and one MICT protocols, which are more commonly used in patients with CAD in the literature on exercise capacity, quality of life, body composition, physical activity level and fear of movement.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: January 1, 2022
• Est. primary completion date: March 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 70 Years

Eligibility

Inclusion Criteria:

• Have undergone percutaneous transluminal coronary angioplasty or coronary artery bypass graft surgery,

• Nonobstructive CAD registered by angiography

• Left ventricular ejection fraction above 50%,

• Clinically stable for more than 2 weeks in terms of symptoms and medical treatment.

Exclusion Criteria:

• Ischemia symptoms,

• Being in Class III-IV according to the New York Heart Classification,

• Obtaining significant left ventricular outflow obstruction,

• Ventricular arrhythmia,

• Being marked valvular heart disease,

• Failure to comply with exercise testing and training rules,

• To have significant orthopedic or neurological comorbidity that prevents full participation.

Related Conditions & MeSH terms

• Cardiac Rehabilitation
• Exercise

Intervention

Other:
• Exercise
Modarete Intensity Continous Training: Medium intensity continuous exercise training will be performed. Exercise intensity will be adjusted as 50-70% of maximal power. High Intensity Interval Training I: It will be four cycles consisting of 4 minute high intensity exercise phase and 3 minute active recovery phase. High intensity phase will be adjusted as 85-100% of maximal power and active recovery phase as 50-70% of maximal power. High Intensity Interval Training II: It will be 10 cycles consisting of 1 minute high intensity exercise phase and 1 minute active recovery phase. High intensity phase will be adjusted as 85-100% of maximal power and active recovery phase as 50-70% of maximal power.

Locations

Country	Name	City	State
Turkey	Kutahya Health Sciences University	Kutahya	Center

Sponsors (1)

Lead Sponsor	Collaborator
Kutahya Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	exercise capacity	Cardiopulmonary exercise test	15 minutes
Secondary	MacNew Health Related Quallity of Life Qustionnaire	The validity and reliability of the MacNew Heart Disease Health-Related Quality of Life Questionnaire Daskapan et al. in 2008. It is a scale developed to determine the quality of life in heart diseases consisting of 27 items each containing a 7-point Likert type response. In the evaluation of the scale, 3 sub-dimensions (emotional, physical and social) and total score values are used	15 minutes
Secondary	body composition	Tanita	1 minute
Secondary	physical activity level	International Physical Activity Questionnaire	15 minutes
Secondary	fear of movement	Tampa	15 minutes