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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04048057
Enrollment
20
Registered
2019-08-07
Start date
2019-07-15
Completion date
2022-01-01
Last updated
2022-08-22

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

Conditions

Cardiac Rehabilitation, Exercise

Brief 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.

Interventions

OTHERExercise

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.

Sponsors

Kutahya Health Sciences University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
exercise capacity15 minutesCardiopulmonary exercise test

Secondary

MeasureTime frameDescription
MacNew Health Related Quallity of Life Qustionnaire15 minutesThe validity and reliability of the MacNew Heart Disease Health-Related Quality of Life Questionnaire Daşkapan 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
body composition1 minuteTanita
physical activity level15 minutesInternational Physical Activity Questionnaire
fear of movement15 minutesTampa

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026