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Clinical Trials/NCT05264701
NCT05264701CompletedNot Applicable

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

Hacettepe University1 site in 1 country52 target enrollmentStarted: April 7, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
52
Locations
1
Primary Endpoint
Exercise Capacity

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
40 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts 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

Arms & Interventions

Physiotherapist Supervised Exercise Training Group

Experimental

Physiotherapist supervised exercise training in patients with coronary artery disease

Intervention: Physiotherapist supervised exercise training (Other)

Exercise Training Tracking from Phone-app Group

Experimental

Exercise training tracking from phone app in patients with coronary artery disease

Intervention: Exercise training via phone app (Other)

Control Group

Experimental

General physical activity recommendations for home

Intervention: Physical activity recommendations (Other)

Outcomes

Primary Outcomes

Exercise Capacity

Time Frame: Baseline, after 12 weeks, after 24 weeks

Exercise capacity will be evaluated using the incremental shuttle walk test.

Participation

Time Frame: after 12 weeks

Participation will be evaluated using the number of sessions attended.

Secondary Outcomes

  • Healthy Living Habit Evaluation(Baseline, after 12 weeks, after 24 weeks)
  • Health-Related Quality of Life(Baseline, after 12 weeks, after 24 weeks)
  • Peripheral muscle strength(Baseline, after 12 weeks, after 24 weeks)
  • Maximal Effort Capacity(Baseline)
  • Endothelial function(Baseline, after 12 weeks, after 24 weeks)
  • QoL(Baseline, after 12 weeks, after 24 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dilara Saklica

Principal Investigator

Hacettepe University

Study Sites (1)

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