Actively Recruiting
Psychological Factors Influencing Cancer Post-traumatic Growth
Led by Centre Hospitalier de Valenciennes · Updated on 2025-03-24
289
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier de Valenciennes
Lead Sponsor
L
Ligue contre le cancer, France
Collaborating Sponsor
AI-Summary
What this Trial Is About
The study focuses on post-traumatic growth (positive changes linked to appreciation of life, personal strengths, social relationships...) in the context of different types of cancer and with a longitudinal approach to the care pathway. The aim of the study is to better understand whether psychological variables (emotional competence, psychological flexibility, psychological distress) and patients' care satisfaction, assessed at the start of the cancer treatment pathway, can influence their post-traumatic growth at the end of the chemotherapy protocol and 6 months later.
CONDITIONS
Official Title
Psychological Factors Influencing Cancer Post-traumatic Growth
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 18 years of age
- Patients in the initial phase of curative treatment for a first solid cancer
- At the start of neo-adjuvant or adjuvant chemotherapy (first or second course)
- Less than 6 months from the initial cancer diagnosis
- Patient has provided written consent to participate in the study
You will not qualify if you...
- Patients with a previous history of cancer
- Patients with incurable cancer progression, recurrence, or relapse
- Patients with metastatic, brain, hematological, or skin cancer
- Patients who have difficulty understanding written French
- Patients psychologically or physically unable to answer questionnaires
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Centre Hospitalier de Valenciennes
Valenciennes, France, 59300
Actively Recruiting
Research Team
A
Anne-Sophie Baudry
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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