Actively Recruiting
Adaptation of the ECCCLORE Program for Patients With Addictive and Traumatic Problems: Feasibility and Acceptability
Led by Centre Hospitalier Universitaire de Nīmes · Updated on 2026-01-28
30
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the feasibility and acceptability of a 12-week adaptation of the ECCCLORE program for patients facing both addiction and trauma-related problems, including complex posttraumatic stress disorder (cPTSD). This condition involves ongoing difficulties with emotion regulation, identity, and relationships after prolonged trauma exposure and is often linked to more severe addiction and behaviors like impulsivity and hostility. The study aims to address these intertwined issues to improve patient quality of life. The intervention being tested is the ECCCLORE program, a cognitive behavioral therapy originally developed for borderline personality disorder, now shortened to 12 weeks for this study. It involves weekly 2-hour group sessions with up to 10 participants, combined with 30-minute individual sessions after each group meeting. Sessions include discussions of the previous week, explanations of key concepts, and practices, plus support for home practice implementation. The program incorporates elements from Acceptance and Commitment Therapy and focuses on emotional regulation, distress tolerance, and interpersonal skills. Participants will be assessed at baseline and after 12 and 24 weeks for trauma, addiction, impulsivity, hostile attribution bias, aggressivity, flexibility, and depression through patient-reported measures. Primary outcomes focus on program feasibility, dropout rates, and acceptability of home practice by week 12. The study excludes certain psychiatric conditions and requires participants to be able to read and write French, with informed consent and health insurance coverage. Participation involves regular therapy sessions and follow-up assessments over the study period.
CONDITIONS
Brief Title
Adaptation of the ECCCLORE Program for Patients With Addictive and Traumatic Problems
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with one or more addictions
- ASSIST questionnaire score ≥ 11 for alcohol and ≥ 4 for other substances
- Diagnosis of PTSD and/or complex PTSD assessed by ITQ scale
- Ability to understand, read, and write French
- Given free and informed consent
- Member or beneficiary of a health insurance plan
You will not qualify if you...
- Participating in another interventional drug or device study or Category 1 study within 3 months
- Under safeguard of justice or state guardianship
- Diagnosis of psychotic disorder
- Severe cognitive impairment (MoCA score < 10)
- Experiencing manic or hypomanic episode
- Experiencing major depressive episode
- Pregnant, parturient, or breastfeeding woman
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 12 weeks
Participants attend weekly group sessions and individual sessions as part of the ECCCLORE program designed to support patients with addiction and trauma issues.
Weekly visits (2-hour group session plus 30-minute individual session)
Trial Site Locations
Total: 1 location
1
CHU de Nîmes
Nîmes, Nîmes, France, 30029
Actively Recruiting
Research Team
L
Laure Thebault
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1