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:
- You have been diagnosed with cervical cancer and your doctors have recommended a specific type of internal radiation treatment called brachytherapy (high-dose rate or pulse-dose rate)
- Your cervical cancer can be of any cell type, including squamous cell carcinoma or others
- You are generally able to carry out daily activities, with at most some limitations (your doctor will assess this using a standard health scale)
- You are able to read and complete questionnaires written in French
- You are willing to give your consent to take part in the study
- You are 18 years old or older
Who may not be able to join:
- You have difficulty understanding or answering questionnaires because of a cognitive condition, a learning disability, a language barrier, or a mental health condition that affects your judgment
- You are currently under a legal protection order (for example, if someone else is legally responsible for making decisions on your behalf)
- You are currently pregnant or breastfeeding
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: George NOEL, MD, PhD, ICANS, CPS
Phone: 368767223
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
Post-Traumatic Stress Disorder evaluation
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.