Depression and Anxiety Trial, Recruiting NCT05703256 Sponsor: Kymberly Young Condition: Depression and Anxiety
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Depression and Anxiety Trial, Recruiting

NCT05703256
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 between 18 and 55 years old
  • People whose primary diagnosis is Major Depressive Disorder (MDD) and who are currently experiencing depression
  • People who are able to provide written consent before taking part
  • People who are either not taking any antidepressant medication, or who have been on a stable antidepressant for at least 4 weeks (existing effective medications would not need to be stopped for this study)

Who may not be able to join:

  • People with significant or unstable heart, lung, hormonal, neurological, or digestive system conditions, or other unstable medical conditions
  • People with a current severe alcohol or substance use disorder (excluding nicotine or caffeine); the trial team would assess mild or moderate alcohol or substance use on a case-by-case basis to decide if it may affect the study (confirm with trial site)
  • People with a history of traumatic brain injury
  • People who are unable to have an MRI scan due to claustrophobia or other MRI-related reasons (such as having metal fragments inside the body)
  • People who are currently pregnant or breastfeeding
  • People who are unable to complete questionnaires written in English
  • People who are currently taking (within 3 weeks of testing) antipsychotics, anticonvulsants, stimulants, benzodiazepines, beta-blockers, or other medications likely to affect blood flow in the brain — not including antidepressants, which would not need to be stopped
  • People diagnosed with a psychotic or organic mental disorder, or with Bipolar I or II disorder
  • People with eye problems or uncorrectable vision difficulties

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.

Contact this trial

Principal Investigator: Kymberly Young, PhD, University of Pittsburgh

Phone: 412-648-6179

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Kymberly Young
Registry
ClinicalTrials.gov
Start date
1 June 2023
Est. completion
30 April 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Beck Depression Inventory (BDI-II)

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