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NCT04002388 Clinical Trial

Objective Measure of Physical Activity and Sedentary Behavior During Cardiac Rehabilitation

Physical Activity Clinical Trial

Official title:
Objective Measure of Physical Activity and Sedentary Behavior During Cardiac Rehabilitation: Are Patients Achieving Recommendations/Guidelines

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04002388
Other study ID # 18-009494
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 2022
Est. completion date March 2022

Study information
Verified date February 2022
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Researchers are trying to assess exercise patterns during and after cardiac rehabilitation participation and to compare changes in blood markers and the microbiome before and after rehabilitation.

Description:

Study participation involves a visit to Mayo Clinic at 6 months and 1 year after you begin cardiac rehabilitation. In addition to the standard of care cardiac rehab program, which consists of 36 full sessions, you would be randomized to an activity monitor group or a usual care group. If randomized to the activity monitor group you will receive a FitBit and will be asked to wear this during cardiac rehabilitation and for one year after you complete the program; complete 4 blood draws (at the start of rehab, at the end of rehab, 6 months after finishing rehab and 1 year after completing rehab) and complete questionnaires about your lifestyle, sleep, mood. The data from the FitBit will be sent to the study team for one year. If randomized to the usual care group you will complete 4 blood draws (at the start of rehab, at the end of rehab, 6 months after rehab, and 1 year after completing rehab); and complete questionnaires about your lifestyle, sleep, mood. If you agree to be in the study, you will be asked to wear monitors with capabilities to detect your heart rate or physical activity for up to 1 year. Data will be acquired from the monitors or remote device accounts. You will also be asked to fill out questionnaires about your current level of physical activity, dietary intake, mood, stress, motivation, and quality of life. You will have a blood draw. You will be asked to complete 2 different stool sample tests, saliva tests, and a fingerstick measure for glycosylated hemoglobin; performed at 4 time points. Information from your medical record will be recorded and used.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date March 2022
Est. primary completion date March 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult 18 years and older - English speaking - Able to provide consent - Has a qualifying indication for cardiac rehabilitation (ie. Acute coronary syndrome, myocardial infarction, percutaneous coronary intervention, coronary artery bypass grafting, and stable angina), owns a smart phone and able to download the fitness monitor app (and willing to have their data downloaded from their fitness monitor after completion of cardiac rehab), and able to participate in cardiac rehabilitation. Exclusion Criteria: - Does not own a smart phone or is unwilling to download the app or is unable to participate in cardiac rehab.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• activity monitor group
will receive a FitBit and will be asked to wear this for one year
• usual care group
will NOT receive a FitBit

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Mayo Clinic

Outcome
Type Measure Description Time frame Safety issue
Primary Physical activity measured by Fitbit (steps) Objective measure of physical activity during cardiac rehabilitation participation and for one year after using a Fitbit and Fitabase. 1 year
Primary Amount of time spent sedentary based on activity counts Objective measure of sedentary time using an accelerometer (activity count levels) 1 year
Primary Change in plasma ceramides Examine the effect of cardiac rehabilitation on plasma ceramide levels 1 year
Secondary Microbiome changes following an exercise program - Cardiac Rehab Examine changes in the microbiome and transcriptome following participation in cardiac based on stool, saliva, and biological markers 15 months
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