Mayo Clinic Proceedings: Digital Health (Sep 2024)

Remote, Smart Device-Based Cardiac Rehabilitation After Myocardial Infarction: A Pilot, Randomized Cross-Over SmartRehab Study

  • Peter Wohlfahrt, MD, PhD,
  • Dominik Jenča, MD,
  • Vojtěch Melenovský, MD, PhD,
  • Jolana Mrázková, Mgr,
  • Marek Šramko, MD, PhD,
  • Martin Kotrč, MD,
  • Michael Želízko, MD,
  • Věra Adámková, MD, PhD,
  • Francisco Lopez-Jimenez, MD, MSc, MBA,
  • Jan Piťha, MD, PhD,
  • Josef Kautzner, MD, PhD

Journal volume & issue
Vol. 2, no. 3
pp. 352 – 360

Abstract

Read online

Objective: To evaluate the effect of smart device-based telerehabilitation on Vo2peak in patients after myocardial infarction. Patients and Methods: This was a pilot, single-center, randomized, cross-over study with a 3-month intervention. One month after myocardial infarction, patients had cardiopulmonary exercise testing and a 6-minute walking test (6MWT) and were randomly assigned 1:1. In the intervention group, patients received a smartwatch to track the recommended number of steps, which was individualized and derived from the 6MWT. A study nurse telemonitored adherence to the recommended number of steps a day. In the control group, 150 minutes a week of moderate-intensity physical activity was recommended. After 3 months study arms were crossed over, and study procedures were repeated after 3 months. Results: Between June 1, 2019, and February 28, 2023, 64 patients were randomized, of which 61 (aged 51±10 years, 10% women) completed the study. Overall, the smart device-based telerehabilitation led to 2.31 mL/kg/min (95% CI, 1.25-3.37; P<.001) Vo2peak increase compared with the control treatment. Furthermore, there was a significant effect on weight (−1.50 kg; 95% CI, −0.39 to −2.70), whereas the effect on the 6MWT distance (4.7 m; 95% CI, −11.8 to 21.1) or Kansas City Quality of Life questionnaire score (0.98; 95% CI, −1.38 to 3.35) was not significant. Conclusion: Smart device-based cardiac rehabilitation may be a promising alternative for patients unable or unwilling to attend in-person cardiac rehabilitation. Trial Registration: clinicaltrials.gov Identifier: NCT03926312