Seated tai chi tested as a way to boost heart health in women with limited mobility
NCT ID NCT07675681
First seen Jun 30, 2026 · Last updated Aug 06, 2026 · Updated 7 times
Summary
This study tests whether a seated Tai Chi and Qigong program, done at home via videos, can improve cardiometabolic health, stress, and sleep in women aged 35-64 who use mobility aids. Participants are randomly assigned to either the Tai Chi program or a health education video group for 12 weeks. Researchers measure changes in waist size, heart rate variability, and stress hormones to see if this gentle mind-body practice offers health benefits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- seated Tai Chi/Qigong
- What this could lead to
- If effective, this could provide an accessible, home-based exercise option to improve cardiometabolic health and well-being for women with mobility impairments.
- What could go wrong
- This is a relatively small, early-stage trial focused on behavioral intervention, so results may not be generalizable. The control group receives health education, which may also provide benefits, making it harder to show a clear advantage.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 280 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2030
An estimate. End dates often move.
- 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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35 to 64 years
- Sex
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Female participants only
- 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.
Show the full entry requirements Hide 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: * Self-identify as a woman. * Age 35-64 years. * Mobility impairment lasting at least 1 year. * Regular use of a mobility aid (e.g., wheelchair, scooter, walker, cane, crutches, or other assistive device). * Community dwelling. * Able to demonstrate sufficient upper-extremity mobility to participate in seated Tai Chi/Qigong activities. * Access to a smartphone, tablet, or computer with internet access. * Willing to wear a study-provided wearable device and complete study assessments. * Reside in the United States. * Waist circumference ≥ 33 inches (84 cm). * Perceived Stress Scale (PSS) score ≥ 15. * Insomnia Severity Index (ISI) score ≥ 8. * Emotional eating indicated by a score \< 3 on the Mindful Eating Questionnaire (MEQ) Emotional Response subscale. * Able to understand written and spoken English. * Able to provide informed consent. * Able to provide healthcare provider approval for participation. Exclusion Criteria: * Medical conditions that would make participation unsafe, as determined during screening. * Inability to safely perform seated upper-body movements. * Current participation in a structured Tai Chi, Qigong, or similar meditative movement program. * Pregnancy, lactation, or plans to become pregnant during the study period. * Cognitive, visual, auditory, or other impairments that would preclude completion of study procedures. * Implanted cardiac devices or implanted electronic devices that interfere with physiologic measurements. * Severe arrhythmia, left ventricular assist device (LVAD), or other conditions that interfere with heart rate variability assessment. * Use of sleep medications three or more times per week. * Medical conditions or medications that substantially affect autonomic nervous system activity, sleep, or stress-related outcomes. * Uncontrolled cardiovascular, neurological, psychiatric, or other serious medical conditions that would preclude safe participation.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Arizona State University
RECRUITINGPhoenix, Arizona, 85004, United States
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