Early Phase 1 Depression and Anxiety Trial, Recruiting NCT07017023 Sponsor: University of Oxford Condition: Depression and Anxiety
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Early Phase 1 Depression and Anxiety Trial, Recruiting

NCT07017023
Recruiting Early Phase 1

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 are willing and able to give their informed consent to take part
  • People aged between 18 and 65 years old
  • People who report experiencing low levels of positive mood
  • People with enough written and spoken English to understand the study procedures
  • People with normal vision and hearing, or vision and hearing that is fully corrected (for example, with glasses or hearing aids)
  • People with access to a computer and a reliable internet connection

Who may not be able to join:

  • People who have taken antidepressant medication in the last three months
  • People who are currently receiving a type of talking therapy called cognitive-behavioural therapy that includes behavioural activation
  • People with a history of psychosis or bipolar disorder
  • People with a history of dependence on alcohol or other substances
  • People who have used illegal drugs in the last three months
  • People who have a parent, sibling, or child with a history of psychosis or bipolar disorder
  • People who have ever been admitted to hospital for mental health reasons
  • People whose score on a standard depression questionnaire (the BDI-II) is above 30, indicating severe depression
  • People who are currently considered to be at clinical risk of suicide
  • People who have previously attempted suicide
  • People who have taken any medication that affects the brain or nervous system in the last six weeks, including as part of another study
  • People who are severely underweight or overweight in a way that the study doctor considers makes them unsuitable for the study
  • People who are currently taking medication for blood pressure or heart conditions
  • People who have been diagnosed with a condition involving low fluid levels or dehydration in the body
  • People with a history of a serious allergic reaction causing swelling (known as angioedema)
  • People who report having impaired kidney function
  • People with consistently very low blood pressure, recorded across at least three separate measurements, where the reading falls below 90/60 mmHg
  • People with a current diagnosis of a developmental condition (such as ADHD, Tourette's syndrome, or a severe learning disability) where the study team believes this would likely affect their ability to complete the study tasks
  • People with a current diagnosis of a neurological condition (such as epilepsy or multiple sclerosis), based on self-report
  • People with a history of serious infection affecting the whole body, or a significant ongoing condition affecting the liver, heart, breathing, kidneys, brain, metabolism, hormones, or lungs, where the study team considers this may affect safety or the ability to take part
  • People who are pregnant, breastfeeding, or planning to become pregnant during the study (a urine pregnancy test is done at the first study visit)
  • People who smoke more than 20 cigarettes per day
  • People with severe lactose intolerance (the study medication contains a small amount of lactose)

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 22 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Principal Investigator: Andrea Reinecke, PhD, University of Oxford

Phone: 01865 618320

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
Early Phase 1
Registry
ClinicalTrials.gov
Start date
8 July 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

Change in reinforcement learning

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: 22 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