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Evaluating Increasing Physical Activity After Acute Coronary Syndrome

Primary Purpose

Physical Activity, Acute Coronary Syndrome

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Financial incentive
Daily feedback
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Physical Activity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Age ≥18 years;
  2. ability to read and provide informed consent to participate in the study;
  3. History of a) acute coronary syndrome (unstable angina, non-ST segment elevation myocardial infarction or ST segment elevation myocardial infarction); or b) patients having undergone coronary catheterization for suspected coronary artery disease.

Exclusion Criteria:

  1. Inability to provide informed consent;
  2. does not have daily access to a smartphone compatible with the wearable device;
  3. unable or unwilling to complete the baseline 6-minute walk test and return to perform the 6-minute walk test at 10 and 18 weeks;
  4. already enrolled in an exercise cardiac rehabilitation program prior to hospital admission;
  5. hemodynamic instability or New York Heart Association III-IV heart failure;
  6. any other medical conditions that would prohibit participation in an 18-week physical activity program;
  7. not being discharged to home if recently admitted.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Control

    Intervention

    Arm Description

    Participants will be given standard exercise recommendations that are given to all patients based on the federal guidelines. They will monitor their step counts using a wearable device and receive daily feedback.

    Participants will be given a wearable device to monitor daily step counts with automated daily feedback on goal attainment via text message or email. A baseline step count will be calculated for each participant (weeks 1-2) and then they will be given a daily step goal with an increase of 15 percentage point each week during the 8-week ramp-up period (weeks 3-10) with a maximum goal of 10,000 steps. Then they'll be asked to maintain that step count (maintenance period). During the ramp-up and maintenance period they'll have a financial incentive of $14 allocated each week and $2 taken away each day the goal is not achieved. They'll be followed up for 8 weeks without incentives

    Outcomes

    Primary Outcome Measures

    Change in Mean Daily Steps
    The primary outcome variable is the change in mean daily step count from the baseline period to the maintenance period (weeks 9-16).

    Secondary Outcome Measures

    Change in Mean Daily Steps From Baseline to Follow-up Period
    Secondary outcomes include change in mean daily steps from the baseline period to the follow-up period (weeks 17-24).

    Full Information

    First Posted
    August 19, 2015
    Last Updated
    July 10, 2019
    Sponsor
    University of Pennsylvania
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02531022
    Brief Title
    Evaluating Increasing Physical Activity After Acute Coronary Syndrome
    Official Title
    A Randomized, Controlled Trial Evaluating Methods to Use Physical Activity to Improve Outcomes After Acute Coronary Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2016 (Actual)
    Primary Completion Date
    February 2017 (Actual)
    Study Completion Date
    April 3, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Pennsylvania

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study will use a randomized, controlled trial to test the effectiveness of a home-based physical activity program using wearable devices and financial incentives. All participants in will establish a baseline step count during the first two weeks and then proceed to a 16-week intervention period and 8-week follow-up period.
    Detailed Description
    Cardiovascular disease is the leading cause of mortality in the United States. Among patients that survive an acute myocardial infarction (AMI), cardiac rehabilitation (CR) has been demonstrated to effectively reduce risk of re-infarction, cardiac mortality, and all-cause mortality. However, despite cardiac rehabilitation being a Class I (standard of care) recommendation in multiple American Heart Association acute myocardial infarction guidelines, more than 80% of eligible patients do not receive appropriate cardiac rehabilitation and much of this is due to challenges in access to these programs. Recent innovations in technology allow us to passively monitor an individual's physical activity using wearable devices. Incentives designed using insights from behavioral economics have been demonstrated to motivate device engagement and behavior change. A remotely-monitored cardiac rehabilitation program could improve access for many individuals and potentially be more cost-effective because it is less resource- and personnel-intensive. The objective of this study is to use a randomized, controlled trial to test the effectiveness of a home-based physical activity program using wearable devices and financial incentives.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Physical Activity, Acute Coronary Syndrome

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    105 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Control
    Arm Type
    Active Comparator
    Arm Description
    Participants will be given standard exercise recommendations that are given to all patients based on the federal guidelines. They will monitor their step counts using a wearable device and receive daily feedback.
    Arm Title
    Intervention
    Arm Type
    Experimental
    Arm Description
    Participants will be given a wearable device to monitor daily step counts with automated daily feedback on goal attainment via text message or email. A baseline step count will be calculated for each participant (weeks 1-2) and then they will be given a daily step goal with an increase of 15 percentage point each week during the 8-week ramp-up period (weeks 3-10) with a maximum goal of 10,000 steps. Then they'll be asked to maintain that step count (maintenance period). During the ramp-up and maintenance period they'll have a financial incentive of $14 allocated each week and $2 taken away each day the goal is not achieved. They'll be followed up for 8 weeks without incentives
    Intervention Type
    Behavioral
    Intervention Name(s)
    Financial incentive
    Intervention Description
    A daily financial incentive framed as a loss of $2 each day goal is not acheived
    Intervention Type
    Behavioral
    Intervention Name(s)
    Daily feedback
    Intervention Description
    Daily feedback from an activity tracking device worn on the wrist to track step counts and sleep patterns
    Primary Outcome Measure Information:
    Title
    Change in Mean Daily Steps
    Description
    The primary outcome variable is the change in mean daily step count from the baseline period to the maintenance period (weeks 9-16).
    Time Frame
    Baseline and end of Maintenance Period at Week 16
    Secondary Outcome Measure Information:
    Title
    Change in Mean Daily Steps From Baseline to Follow-up Period
    Description
    Secondary outcomes include change in mean daily steps from the baseline period to the follow-up period (weeks 17-24).
    Time Frame
    Baseline and end of Follow Up Period at week 24

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Age ≥18 years; ability to read and provide informed consent to participate in the study; History of a) acute coronary syndrome (unstable angina, non-ST segment elevation myocardial infarction or ST segment elevation myocardial infarction); or b) patients having undergone coronary catheterization for suspected coronary artery disease. Exclusion Criteria: Inability to provide informed consent; does not have daily access to a smartphone compatible with the wearable device; unable or unwilling to complete the baseline 6-minute walk test and return to perform the 6-minute walk test at 10 and 18 weeks; already enrolled in an exercise cardiac rehabilitation program prior to hospital admission; hemodynamic instability or New York Heart Association III-IV heart failure; any other medical conditions that would prohibit participation in an 18-week physical activity program; not being discharged to home if recently admitted.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mitesh Patel, MD, MBA, MS
    Organizational Affiliation
    University of Pennsylvania
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    32254044
    Citation
    Fortunato M, Adusumalli S, Chokshi N, Harrison J, Rareshide C, Patel M. Usability of Wearable Devices to Remotely Monitor Sleep Patterns Among Patients With Ischemic Heart Disease: Observational Study. JMIR Form Res. 2020 Apr 7;4(4):e14508. doi: 10.2196/14508.
    Results Reference
    derived
    PubMed Identifier
    29899015
    Citation
    Chokshi NP, Adusumalli S, Small DS, Morris A, Feingold J, Ha YP, Lynch MD, Rareshide CAL, Hilbert V, Patel MS. Loss-Framed Financial Incentives and Personalized Goal-Setting to Increase Physical Activity Among Ischemic Heart Disease Patients Using Wearable Devices: The ACTIVE REWARD Randomized Trial. J Am Heart Assoc. 2018 Jun 13;7(12):e009173. doi: 10.1161/JAHA.118.009173.
    Results Reference
    derived

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    Evaluating Increasing Physical Activity After Acute Coronary Syndrome

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