Investigating KardioPAC Mobile App to Improve Physical Fitness Among Cardiac Rehabilitation Patients

Not Applicable

Active, not recruiting

• Conditions: Cardiac Rehabilitation; Quality of Life; Exercise

• Registration Number: NCT05643976
• Lead Sponsor: University of California, San Diego

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-11-16
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion Criteria:<br><br> 1. Referred to the University of California San Diego Health Cardiac Rehabilitation<br> Center for 36-72 sessions of intensive cardiac rehabilitation for one of the<br> following medical conditions: myocardial infarction, coronary artery bypass surgery,<br> stable angina, heart valve repair or replacement, coronary angioplasty or stenting,<br> congestive heart failure, heart transplant, or peripheral arterial disease<br><br> 2. Able to give informed consent in English<br><br> 3. Able to perform study assessments as described<br><br> 4. Resting BP<180/110 mmHg<br><br> 5. Able to perform light to moderate exercise<br><br> 6. Have not had a fall during the previous 6 months resulting in an injury<br><br> 7. Clinical staff's permission to participate, including their assessment that<br> participant is a good candidate for this research study<br><br> 8. Ability to complete written or app-based surveys<br><br> 9. Owns an Apple or Android mobile telephone capable of downloading and running the app<br><br>Exclusion Criteria:<br><br> 1. Referred to CR following Ventricular Assist Device procedure<br><br> 2. Angina not adequately managed with nitrates<br><br> 3. Oxygen-dependent Chronic Obstructive Pulmonary Disease<br><br> 4. Recent stroke or significant cerebral neurologic impairment that would interfere<br> with participation.<br><br> 5. Unable to operate a BP device

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Delta change in minutes per week of moderate physical activity between baseline and end of study between SOC and intervention as measured by actigraphy.

Secondary Outcome Measures

Name	Time	Method
Health-related quality of life as measured by the 29-item Patient-Reported Outcomes Measurement Information System (PROMIS®-29)