Depression and Anxiety Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with Generalized Anxiety Disorder (GAD) by a psychiatrist using standard diagnostic guidelines (DSM-V).
- People whose first language is Chinese.
- People who are right-handed.
- People who have normal vision, either naturally or with glasses or contact lenses.
- People who have normal hearing and are able to speak and express themselves verbally.
- People who are able to attend regular medical or psychological check-ins throughout the study period.
Who may not be able to join:
- People who have been diagnosed with other significant neurological or mental health conditions besides GAD.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +886911164386
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in cerebral hemodynamics from functional near-infrared spectroscopy (fNIRS); Change in severity of physiological and psychological anxious symptoms as assessed by Hamilton Anxiety Rating Scale (HARS); Change in temporary and long-term anxiety levels as assessed by State-Trait Anxiety Inventory (STAI); Change in anxiety level as reported in Visual Analog Scale (VAS); Change in physiological anxious symptoms indicated by Heart Rate Variability (HRV)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.