Tai chi and tech team up to get heart patients moving
NCT ID NCT05699642
First seen Jun 27, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This study looks at whether tai chi exercises and wearable fitness trackers can help people who have survived a heart attack (acute coronary syndrome) become more physically active. About 70 adults who are currently inactive will take part. The goal is to see if this approach is enjoyable and helps people stick with exercise.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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70 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. History of ACS (unstable angina, NSTEMI, and STEMI, defined per current AHA/ACC criteria); 2. Age ≥ 18; 3. Being physically inactive (i.e., \< 150 min/week of moderate-intensity aerobic PA); 4. Absence of contraindications to physical exercise per the participant's provider evaluation; 5. Access to a digital device with internet connection; 6. Having an active email account and ability to check email at least weekly; 7. 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; 8. English speaking Exclusion Criteria: 1. Inability or unwillingness to give informed consent; 2. Blood pressure \>200/110 or orthostatic systolic blood pressure decrease \>20 mmHg at the baseline visit; 3. Uncontrolled/untreated atrial or ventricular arrhythmias or 3rd degree AV block; 4. Within 3 months of a diagnosis of pericarditis or myocarditis; 5. Medical conditions likely to limit lifespan to less than one year; 6. New York Heart Association (NYHA) functional class IV; 7. Severe cognitive impairment (BOMC \>10);139 8. Orthopedic problems prohibiting TC practice; 9. Ongoing TC or other mind-body training (i.e., meditation, TC, or yoga) at least weekly; 10. Current enrollment in cardiac rehabilitation; 11. Untreated severe depression (PHQ\>=20); 12. Conditions likely to affect study compliance (i.e., moving out of study area, substance use, ongoing untreated psychosis); 13. Symptoms of unstable cardiovascular disease (e.g., shortness of breath or chest pain at rest and/or Canadian Cardiovascular Society Angina Class III-IV)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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