PTSD Trial, Recruiting

Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

For patients (Part 1):

• Adults aged 18 or older
• People diagnosed with breast, gynaecological, testicular, or digestive cancer within the last 4 months, at the point when their treatment plan was first explained to them
• People whose cancer requires active cancer treatment
• People who are starting their cancer treatment at the Oscar Lambret Center
• People whose cancer has not spread to the brain or central nervous system
• People with a favourable prognosis score (PRONOPALL score of 3 or less) or an expected survival of more than 6 months (confirm with trial site)
• People who have signed consent to participate and are covered by French social security
• People who are able to identify a caregiver — such as a family member, friend, or other person who has helped support them since their diagnosis
• People who have access to a computer or tablet with an internet connection for completing online questionnaires; a webcam is needed if video participation is preferred, or a smartphone capable of video calls if phone-based video is preferred

For caregivers (Part 1):

• Adults aged 18 or older
• People designated by the patient as their primary caregiver (a family member, friend, or other person who has helped care for the patient since diagnosis)
• People who have signed consent to participate
• People who have access to a computer or tablet with an internet connection; a webcam is needed if video participation is preferred, or a smartphone capable of video calls if phone-based video is preferred

For patient focus groups (Part 2):

• Adults who have or have had cancer
• Members of a local patient association or the Oscar Lambret Center's patient partners committee, or people who completed all three steps of Part 1 of this study
• People with access to a computer or tablet with a camera and internet connection
• People who have given consent to participate

For caregiver focus groups (Part 2):

• Adults who are, or have been, a caregiver for a person with cancer
• Members of a local caregivers' association, or people who completed all three steps of Part 1 of this study
• People with access to a computer or tablet with a camera and internet connection
• People who have given consent to participate

For healthcare professional focus groups (Part 2):

• Medical or paramedical staff at the Oscar Lambret Center, or non-hospital professionals involved in the medical or psychological care of patients
• Professionals who are not already involved in running this study
• People with access to a computer or tablet with a camera and internet connection
• People who have given consent to participate

Who may not be able to join:

For patients (Part 1):

• People whose cancer has spread to the brain or the membranes surrounding the brain
• People whose cancer has come back after a previous illness (recurrence)
• People living with a psychiatric or neurological condition that may affect their ability to reason or make judgements — such as a psychotic disorder, autism spectrum disorder, or intellectual disability
• People who, as confirmed by medical staff, are unable to complete questionnaires due to psychological or physical reasons
• People who are under a custodial sentence, guardianship, or legal protection for vulnerable adults

For caregivers (Part 1):

• People living with, or suspected of having, a psychiatric or neurological condition that may affect their ability to reason or make judgements — such as a psychotic disorder, autism spectrum disorder, or intellectual disability (this criterion is self-reported; no additional tests are required)
• People who are unable to complete questionnaires due to psychological or physical reasons, or where there is a suspicion of this (self-reported; no additional tests are required)
• People who are under a custodial sentence, guardianship, or legal protection for vulnerable adults

For focus group participants from Part 1:

• People who did not complete all three required measurement points during Part 1 of the study

Important: Always verify eligibility with the trial site directly before applying.