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N/A Completed N=105 Randomized Health Services Research

Evaluating Increasing Physical Activity After Acute Coronary Syndrome

Physical Activity · Coronary Artery Disease
Source: ClinicalTrials.gov NCT02531022 ↗
Enrolled (actual)
105
Serious AEs
0.0%
Results posted
Jul 2019
Primary outcomePrimary: Change in Mean Daily Steps — 264; 1501 Steps

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.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Mean Daily Steps
264; 1501
SECONDARY
Change in Mean Daily Steps From Baseline to Follow-up Period
92; 1066

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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02531022). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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