Investigation of the Effects of the Technology-based Cardiac Rehabilitation Program in Coronary Artery Patients
NCT ID: NCT05264701
Last Updated: 2024-06-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
52 participants
INTERVENTIONAL
2022-04-07
2024-05-01
Brief Summary
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Detailed Description
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This study was planned to investigate the effectiveness of technology-based and traditional cardiac rehabilitation programs in individuals with coronary artery disease.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Physiotherapist Supervised Exercise Training Group
Physiotherapist supervised exercise training in patients with coronary artery disease
Physiotherapist supervised exercise training
Exercise training for 12 weeks will be given by video talk accompanied by a physiotherapist.
Exercise Training Tracking from Phone-app Group
Exercise training tracking from phone app in patients with coronary artery disease
Exercise training via phone app
Exercise training for 12 weeks will be given over the developed phone application.
Control Group
General physical activity recommendations for home
Physical activity recommendations
The program will be consist of 12 weeks of physical activity recommendations.
Interventions
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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.
Eligibility Criteria
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Inclusion Criteria
* Access to the online program
* Volunteering to participate in the research
* Having an iOS or Android operating system compatible phone
Exclusion Criteria
* 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
40 Years
70 Years
ALL
No
Sponsors
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Hacettepe University
OTHER
Responsible Party
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Dilara Saklica
Principal Investigator
Principal Investigators
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Naciye Vardar-Yagli, PhD
Role: STUDY_DIRECTOR
Hacettepe University
Hikmet Yorgun, PhD
Role: STUDY_DIRECTOR
Hacettepe University
Ahmet Hakan Ates, PhD
Role: STUDY_CHAIR
Hacettepe University
Deniz Yuce, PhD
Role: STUDY_CHAIR
Hacettepe University
Dilara Saklica, MSc
Role: PRINCIPAL_INVESTIGATOR
Hacettepe University
Locations
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Hacettepe University
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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KA-20105
Identifier Type: -
Identifier Source: org_study_id
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