Investigation of the Effects of the Technology-based Cardiac Rehabilitation Program in Coronary Artery Patients

Coronary Artery Disease Clinical Trial

Official title:

Investigation of the Effects of Artificial Intelligence-supported and Technology-based Cardiac Rehabilitation Programs on Participation and Exercise Capacity in Coronary Artery Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05264701
• Other study ID #: KA-20105
• Status: Completed
• Phase: N/A
• Start date: April 7, 2022
• Est. completion date: May 1, 2024

Study information

• Verified date: June 2024
• Source: Hacettepe University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study was planned to investigate the effectiveness of technology-based and traditional cardiac rehabilitation programs in individuals with coronary artery disease.

Description:

Cardiovascular diseases constitute one of the most critical health problems of today's society due to the loss of workforce, morbidity, mortality, and high hospital expenses. This study was planned to investigate the effectiveness of technology-based and traditional cardiac rehabilitation programs in individuals with coronary artery disease.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: May 1, 2024
• Est. primary completion date: May 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 70 Years

Eligibility

Inclusion Criteria:

• Patients with coronary artery disease
• Access to the online program
• Volunteering to participate in the research
• Having an iOS or Android operating system compatible phone

Exclusion Criteria:

• Having a musculoskeletal problem
• Having uncontrolled hypertension
• Having chronic heart failure (NYHA III-IV)
• A history of acute coronary syndrome or surgical revascularization less than 12 months ago
• More than 50% occlusion on the main coronary artery
• Having arrhythmia

Related Conditions & MeSH terms

• Coronary Artery Disease
• Physical Inactivity

Intervention

Other:
• Physiotherapist supervised exercise training
Exercise training for 12 weeks will be given by video talk accompanied by a physiotherapist.
• Exercise training via phone app
Exercise training for 12 weeks will be given over the developed phone application.
• Physical activity recommendations
The program will be consist of 12 weeks of physical activity recommendations.

Locations

Country	Name	City	State
Turkey	Hacettepe University	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Exercise Capacity	Exercise capacity will be evaluated using the incremental shuttle walk test.	Baseline, after 12 weeks, after 24 weeks
Primary	Participation	Participation will be evaluated using the number of sessions attended.	after 12 weeks
Secondary	Maximal Effort Capacity	Maximal effort capacity will be evaluated using a cardiovascular stress test.	Baseline
Secondary	Peripheral muscle strength	Peripheral muscle strength will be evaluated using the dynamometer.	Baseline, after 12 weeks, after 24 weeks
Secondary	Endothelial function	The endothelial function will be evaluated using echocardiography. After a resting baseline, Brachial artery diameter will be recorded, the cuff used in blood pressure measurement will be inflated 25-50 mmHg above the systolic blood pressure value and maintain that pressure for 5 min. The brachial artery diameter will be measured again after the cuff is deflated.	Baseline, after 12 weeks, after 24 weeks
Secondary	Healthy Living Habit Evaluation	Healthy living habit evaluation will be evaluated using the Healthy Lifestyle Behaviors Scale-II.	Baseline, after 12 weeks, after 24 weeks
Secondary	Health-Related Quality of Life	Health-Related Quality of Life will be evaluated using the Myocardial Infarction Dimensional Assessment Scale (MIDAS).	Baseline, after 12 weeks, after 24 weeks
Secondary	QoL	Quality of life will be evaluated using the SF-36 Short Form.	Baseline, after 12 weeks, after 24 weeks