Actively Recruiting
Self-Identification Program
Led by University Hospital, Montpellier · Updated on 2025-09-30
86
Participants Needed
1
Research Sites
179 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Conduct a pilot, single-center, randomized controlled 2-arm study aimed to evaluate the impact of an in-depth 3rd wave CBT program targeting correct self-identification (3rd level of 3rd wave CBT), compared to a control group receiving an acceptance and commitment therapy (ACT; (1st level of 3rd wave CBT, a well-known psychotherapy). Main judgment criteria : Therapeutic response (reduction ≥ 50% between pre and immediate post-treatment), and rate of relapse at 6 months post-therapy. Secondary objectives: Evaluate psychological processes involved in the reduction of moral pain, diligence, ruminations, suicidal ideas, self-concept and alterations in functioning (mental and social), psychological skills.
CONDITIONS
Official Title
Self-Identification Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 70 years
- Presenting a current major depressive episode according to DSM 571
- Diagnosis may be part of unipolar or bipolar depressive disorder
You will not qualify if you...
- Patients with a psychotic disorder
- Active suicidal thoughts with intention to act (C-SSRS ideation score 4 in the last week)
- Unable to receive informed information about the study
- Exclusion period due to participation in a previous study
- Adults under legal protection such as guardianship or curatorship
- Not affiliated with or beneficiary of a French social security scheme
- Unable to give informed written consent
- Pregnant or breastfeeding women
- Patients under judicial protection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Montpellier
Montpellier, France
Actively Recruiting
Research Team
D
Déborah Ducasse, MD
CONTACT
V
Véronique Brand Arpon, IDE
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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