Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Combined brain stimulation and yoga for improving cognition in psychosis

Official title: Yoga and tDCS to Improve Cognitive Function in Individuals With Psychosis: A Pragmatic Controlled Trial

Run by The Hong Kong Polytechnic University · NCT07747181 · Data updated 2026-11-12

This study tests whether active brain stimulation plus yoga can improve thinking skills and daily function in adults with psychosis.

More Psychosis trials

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment135 (estimated)
SponsorThe Hong Kong Polytechnic University
Academic / other
Locations1 site (Hung Hom, Kowloon)
StatusRecruiting
StartedJanuary 1, 2026
Main results expectedDecember 31, 2027
Study endsJune 30, 2028
Registry record updatedAugust 5, 2026
Trial IDNCT07747181 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18-65 with psychosis who meet SCID criteria and have CGI positive symptoms ≤ 3, are Chinese-speaking, and have minimal recent mind-body intervention exposure.

Probably not a fit

Individuals with significant comorbid physical conditions, certain contraindications to exercise or fNIRS, or those extensively engaged in mind-body practices may not benefit.

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

What this trial studies

This interventional study explores whether anodal tDCS paired with a yoga program can enhance cognitive function, symptoms, and quality of life in people with psychosis. It will compare active tDCS, sham tDCS, and yoga as part of the intervention strategy. Neurophysiological changes will be examined to understand how the combined approach may produce effects. Participants are adults with psychosis who meet specific diagnostic and consent criteria and have limited prior exposure to mind-body practices. The Hong Kong Polytechnic University serves as the lead site for this research.

Why it matters

Potential benefit: If successful, participants may experience improvements in cognitive function and broader quality-of-life benefits.

How similar studies have gone: Prior studies in related domains suggest potential cognitive benefits from brain stimulation and mind-body interventions, though combining them in psychosis is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* (1) aged 18 to 65 years
* (2) diagnosis based on SCID for schizophrenia and related disorders, psychosis, and delusional disorder with the positive symptom measured by CGI ≤ 3
* (3) ability to understand the nature of the study and to give informed consent (The MacArthur Competence Assessment Tool for Clinical Research score ≥ 35)
* (4) Chinese-speaking
* (5) fewer than 10 hours of yoga and other mind-body intervention (e.g., Tai Chi, Qigong, Mindfulness) in the previous 3 months.

Exclusion Criteria:

* (1) Severe physical diseases, such as myocardial infarction, uncontrollable severe hypertension, fracture, severe spinal problems, or contraindication for exercise
* (2) comorbid substance dependence and seizure disorders
* (3) pregnancy or other contraindication to fNIRS
* (4) known history of intellectual disability or special school attendance, brain trauma, or organic brain disease
* (5) Individuals taking Benzodiazepine will still be recruited in the project, and will be excluded from the fNIRS measure.

Where it's running

  • The Hong Kong Polytechnic University
    Hung Hom, Kowloon, Hong Kong
    Recruiting

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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.