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Tai chi and tech team up to get heart patients moving

NCT ID NCT05699642

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

70 people

The number who actually took part.

Started

Aug 2024

Finished

Jul 2026

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

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.

acute coronary syndrome Sedentary Behavior

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02215, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.