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NCT05699642CompletedPhase 2

Online Tai Chi Plus Fitbit After ACS

Tai Chi Exercise and Wearable Feedback Technology to Promote Physical Activity in Acute Coronary Syndrome Survivors

Source: ClinicalTrials.gov · Last updated 6 Aug 2026

Brief summary (registry, in English)

This projects studies the role of tai chi exercise and wearable fitness trackers to promote physical activity in acute coronary syndrome (ACS) survivors.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
70 (actual)
First submitted
6 Jan 2023
Start date
Aug 2024
Primary completion date
Jul 2026
Lead sponsor
Beth Israel Deaconess Medical Center
NCT number
NCT05699642

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 70
  • From Aug 2024 to the primary completion date, Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Uncontrolled/untreated atrial or ventricular arrhythmias or 3rd degree AV block;
  • Medical conditions likely to limit lifespan to less than one year;
  • New York Heart Association (NYHA) functional class IV;
  • Severe cognitive impairment (BOMC \>10);139
  • Current enrollment in cardiac rehabilitation;
  • Conditions likely to affect study compliance (i.e., moving out of study area, substance use, ongoing untreated psychosis);
  • Symptoms of unstable cardiovascular disease (e.g., shortness of breath or chest pain at rest and/or Canadian Cardiovascular Society Angina Class III-IV)

Other

  • Inability or unwillingness to give informed consent;
  • Blood pressure \>200/110 or orthostatic systolic blood pressure decrease \>20 mmHg at the baseline visit;
  • Within 3 months of a diagnosis of pericarditis or myocarditis;
  • Orthopedic problems prohibiting TC practice;
  • Ongoing TC or other mind-body training (i.e., meditation, TC, or yoga) at least weekly;
  • Untreated severe depression (PHQ\>=20);

Who the study is looking for

  • History of ACS (unstable angina, NSTEMI, and STEMI, defined per current AHA/ACC criteria);
  • Age ≥ 18;
  • Being physically inactive (i.e., \< 150 min/week of moderate-intensity aerobic PA);
  • Absence of contraindications to physical exercise per the participant's provider evaluation;
  • Access to a digital device with internet connection;
  • Having an active email account and ability to check email at least weekly;
  • Physician clearance to participate in low-moderate intensity exercise (tai chi), including a statement that there is no contraindication to exercise based on post-ACS stress test and other factors, as appropriate;
  • English speaking

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Beth Israel Deaconess Medical Center
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.