Depression and Anxiety Trial, Recruiting NCT06936059 Sponsor: Xinhua Hospital, Shanghai Jiao Tong University School of Medicine Condition: Depression and Anxiety
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Depression and Anxiety Trial, Recruiting

NCT06936059
Recruiting Not Applicable

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 aged 18 or older, of any gender
  • People whose pain level has been at least 4 out of 10 (on average) over the past 24 hours
  • People who can speak, read, and write in Chinese
  • People who are willing to follow the study's procedures and rules
  • People who are willing and able to sign a consent form agreeing to take part

Who may not be able to join:

  • People whose shingles affects the eyes, ears, head, face, or hands
  • People who have trigeminal neuralgia (a nerve pain condition affecting the face)
  • People with severe vision problems (those with clear vision when wearing glasses or contact lenses may still be considered)
  • People with severe hearing problems
  • People with a medical condition that makes nausea or dizziness more likely, such as reduced blood supply to the brain, balance disorders, or gallbladder inflammation
  • People with a history of severe motion sickness
  • People with an injury to the eyes, ears, face, or neck that would make wearing a mixed reality headset uncomfortable or difficult
  • People with an injury or condition affecting the hands or arms that would make using a mixed reality device uncomfortable or difficult
  • People diagnosed with cognitive impairment, epilepsy, dementia, migraines, or other neurological conditions that may prevent safe use of mixed reality technology
  • People with a history of mental illness, including depression, generalised anxiety disorder, or schizophrenia
  • People who are currently pregnant
  • People who are currently taking part in, or who completed another interventional clinical trial within the 4 weeks before screening
  • People the trial investigators consider unsuitable for the study for any other reason (confirm with trial site)

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Registry
ClinicalTrials.gov
Start date
12 November 2025
Est. completion
12 November 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Change in pain intensity before and after MR therapy

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov