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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05264701
Enrollment
52
Registered
2022-03-03
Start date
2022-04-07
Completion date
2024-05-01
Last updated
2024-06-18

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

Conditions

Coronary Artery Disease, Physical Inactivity

Keywords

Cardiac Rehabilitation, Exercise Training

Brief summary

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

Detailed 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.

Interventions

OTHERPhysiotherapist supervised exercise training

Exercise training for 12 weeks will be given by video talk accompanied by a physiotherapist.

OTHERExercise training via phone app

Exercise training for 12 weeks will be given over the developed phone application.

The program will be consist of 12 weeks of physical activity recommendations.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Exercise CapacityBaseline, after 12 weeks, after 24 weeksExercise capacity will be evaluated using the incremental shuttle walk test.
Participationafter 12 weeksParticipation will be evaluated using the number of sessions attended.

Secondary

MeasureTime frameDescription
Endothelial functionBaseline, after 12 weeks, after 24 weeksThe 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.
Healthy Living Habit EvaluationBaseline, after 12 weeks, after 24 weeksHealthy living habit evaluation will be evaluated using the Healthy Lifestyle Behaviors Scale-II.
Maximal Effort CapacityBaselineMaximal effort capacity will be evaluated using a cardiovascular stress test.
QoLBaseline, after 12 weeks, after 24 weeksQuality of life will be evaluated using the SF-36 Short Form.
Health-Related Quality of LifeBaseline, after 12 weeks, after 24 weeksHealth-Related Quality of Life will be evaluated using the Myocardial Infarction Dimensional Assessment Scale (MIDAS).
Peripheral muscle strengthBaseline, after 12 weeks, after 24 weeksPeripheral muscle strength will be evaluated using the dynamometer.

Countries

Turkey (Türkiye)

Outcome results

None listed

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