Clinical trial Recruiting at 1 site Interventional Ages 19 and up

Mindfulness practice with Tao art to improve well-being

Official title: The Effects of Mindfulness Practice With Tao Art (Love Peace Harmony Calligraphy and Song) on Well-being - Controlled Randomized Study

Run by Sha Research Foundation · NCT06803641 · Data updated 2026-11-12

This study is testing if a special mindfulness practice using Tao art can help adults feel less stressed and more connected to others.

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Quick facts

Study typeInterventional
Ages19 Years and up
SexAll
Enrollment50 (estimated)
SponsorSha Research Foundation
Academic / other
Locations1 site (Buffalo, New York)
StatusRecruiting
StartedApril 5, 2025
Main results expectedJuly 31, 2030
Study endsDecember 31, 2030
Registry record updatedApril 28, 2026
Trial IDNCT06803641 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 19 and over who are willing to engage in daily mindfulness practices for at least 30 minutes.

Probably not a fit

Patients with serious mental disorders or those unable to comply with the practice regimen may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical study aims to evaluate the effects of a unique mindfulness practice involving Tao art, specifically the 'Love Peace Harmony' calligraphy and song, on adult well-being. Participants will be randomized into either a mindfulness practice group or a wait-list control group. The study will measure changes in perceived stress, social connectedness, and peace of mind using standardized questionnaires before and after three months of practice. Statistical analyses will be conducted to determine the significance of any observed changes.

Why it matters

Potential benefit: If successful, this approach could enhance well-being by reducing stress and improving social connections and peace of mind for participants.

How similar studies have gone: While mindfulness practices have been widely studied, the specific use of Tao art in this context is relatively novel and has not been extensively tested in previous studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria

* Age 19 and over
* Willingness and ability to comply with data collection requirements
* Submission of required documentation before entering the study, including informed consent and consent to release of information
* Willingness to allow their data to be used for research purposes and published as deemed fit (while conforming to all applicable privacy laws) by Sha Research Foundation
* Willingness to practice the daily mindfulness practices for at least 30 minutes and follow the study protocol

Exclusion criteria

* Not meeting any of the inclusion criteria
* Unwillingness to participate in data gathering
* Unable to follow the practice regimen, including the daily individual mindfulness practices for at least 30 minutes
* Pregnant or nursing. Participants who become pregnant during the study will be required to end their participation.
* Serious mental disorders (e.g., schizophrenia)
* There is no exclusion criteria placed upon potential subjects related to national origin, culture, ethnicity, race, sex, physical disability, sexual orientation, religion, or spiritual practices.

Where it's running

  • Private practice (Psychology)
    Buffalo, New York, United States
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.