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

Assessing the Ability of KardioPAC, a Digital Tool, to Facilitate Lifestyle Change in Participants Enrolled in a Cardiac Rehabilitation Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05643976
Enrollment
43
Registered
2022-12-09
Start date
2023-01-18
Completion date
2024-11-30
Last updated
2025-10-29

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

Conditions

Cardiac Rehabilitation, Exercise, Quality of Life

Brief summary

The purpose of this study is to sustain regular physical activity, improve health-related quality of life, improve resting blood pressure, improve anthropometrics, and improve adherence to prescribed cardiac rehabilitation sessions among individuals referred for cardiac rehabilitation (CR). Numerous studies show that CR improves clinical outcomes in cardiovascular disease (CVD). Exercise as a reliable adjunctive intervention, however, remains limited due to poor short- and long-term adherence. This proposed study will examine the effectiveness of the Kura Care KardioPac digital application plus CR to significantly sustain exercise adherence among CR patients, as compared to standard of care alone.

Interventions

BEHAVIORALKardioPAC Mobile Application

Like those in the SOC CR arm, participants assigned to the CR+KardioPAC arm will receive standard of care and attend CR as prescribed by their physician. Additionally, they will receive access to the digital app, KardioPAC, & a BP device for home use that will record their BP readings in the app. KardioPAC is a remote patient monitoring system that allows providers to monitor patients and send out daily reminders. It integrates with BP monitors and fitness watches to collect patient health information at home. The information is uploaded to the HIPAA-compliant server and presented on the website for providers to read. Its reminder system can be customized to meet diverse clinical needs. Lastly, the Kura Care in-house Registered Nurse will provide 20-30 min of health coaching to intervention arm participants on a weekly or bi-weekly basis via the app. The coaching will include greetings, review of medication adherence, encouragement to exercise, and symptom management, if applicable.

OTHERStandard of Care

During the prescribed cardiac rehabilitation, the SOC CR intervention participants will receive standard of care by attending the 36-72 sessions of CR as prescribed by his/her physician and administered by the University of California San Diego Health Cardiac Rehabilitation Center.

Sponsors

University of California, San Diego
Lead SponsorOTHER
KURA Care
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Referred to the University of California San Diego Health Cardiac Rehabilitation Center for 36-72 sessions of intensive cardiac rehabilitation for one of the following medical conditions: myocardial infarction, coronary artery bypass surgery, stable angina, heart valve repair or replacement, coronary angioplasty or stenting, congestive heart failure, heart transplant, or peripheral arterial disease 2. Able to give informed consent in English 3. Able to perform study assessments as described 4. Resting BP\<180/110 mmHg 5. Able to perform light to moderate exercise 6. Have not had a fall during the previous 6 months resulting in an injury 7. Clinical staff's permission to participate, including their assessment that participant is a good candidate for this research study 8. Ability to complete written or app-based surveys 9. Owns an Apple or Android mobile telephone capable of downloading and running the app

Exclusion criteria

1. Referred to CR following Ventricular Assist Device procedure 2. Angina not adequately managed with nitrates 3. Oxygen-dependent Chronic Obstructive Pulmonary Disease 4. Recent stroke or significant cerebral neurologic impairment that would interfere with participation. 5. Unable to operate a BP device

Design outcomes

Primary

MeasureTime frameDescription
Delta change in minutes per week of moderate physical activity between baseline and end of study between SOC and intervention as measured by actigraphy.~4 MonthsAssess the ability of CR + KardioPAC as compared to standard-of-care CR to change the activity level of participants.

Secondary

MeasureTime frameDescription
Delta change in METs (Metabolic Equivalents of Task), a measure of the amount of oxygen consumed during activity compared to resting oxygen consumption.~4 MonthsAssess the ability of CR + KardioPAC as compared to standard-of-care CR to improve functional capacity (METs) at pre- and post-CR.

Other

MeasureTime frameDescription
Resting Blood Pressure~4 MonthsAssess the ability of CR + KardioPAC as compared to standard-of-care CR to change resting blood pressure at pre- and post-CR.
Body Composition~4 MonthsAssess the ability of CR + KardioPAC as compared to standard-of-care CR to change body composition at pre- and post-CR.

Countries

United States

Outcome results

None listed

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