PTSD 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:
For Phases 1 and 2 of the study:
- Women aged 18 to 45 who are currently pregnant (at any stage of pregnancy) and are willing and able to give informed consent.
- Women aged 18 to 45 who have given birth within the past 1 to 12 months and are willing and able to give informed consent.
- Women aged 18 to 45 who are not currently pregnant and have not given birth in the past 12 months, and are willing and able to give informed consent.
For Phase 3 of the study:
- Women aged 18 to 45 who are in early pregnancy (before 20 weeks) at the time of joining, are not planning to move away during the study, are willing and able to give informed consent, and are willing to attend four planned visits.
- Women aged 18 to 45 who are not currently pregnant and have not given birth in the last 12 months, are not planning to move away during the study, are willing and able to give informed consent, and are willing to attend four planned visits.
Who may not be able to join:
- People with a severe and acute psychiatric illness that affects their ability to take part in the study.
- People who are not willing or able to give informed consent.
The trial notes that having a current or past physical, psychological, or psychiatric condition does not automatically prevent participation, as long as the ability to take part and give informed consent is not affected (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.
Contact this trial
Principal Investigator: Gracia Fellmeth, DPhil, University of Oxford
Phone: 00441865289745
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
Phase 1: Codes and themes relating to acceptability of screening for perinatal mental disorders; Phase 2: Psychometric properties of screening tools for common mental disorders; Phase 3: Point prevalence, period prevalence and incidence (with 95% confidence intervals) of common mental disorders among perinatal and non-perinatal women; Phase 3: Odds ratios (with 95% confidence intervals) for factors associated with common mental disorders among perinatal and non-perinatal women
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.