Actively Recruiting
Effectiveness of a Cognitive and Behavioral Treatment Program in People With Idiopathic Environmental Intolerance (IEI)
Led by Institut National de la Santé Et de la Recherche Médicale, France · Updated on 2025-08-13
82
Participants Needed
1
Research Sites
245 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Idiopathic Environmental Intolerance (IEI) denotes a functional disorder represented by heterogeneous symptoms that sufferers attribute to specific environmental agents and for which there may be no solid evidence of an underlying physiological cause. We are conducting a randomized controlled trial study to compare patients before and after a newly developed cognitive behavioral therapy treatment program for IEI, with respect to behavioral and psychometric variables. The results of this research project are expected to contribute to advancements in the clinical treatment of IEI, as well as to elaborate on existing theoretical models of IEI.
CONDITIONS
Official Title
Effectiveness of a Cognitive and Behavioral Treatment Program in People With Idiopathic Environmental Intolerance (IEI)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 9 years
- Present a diagnosis of idiopathic environmental intolerance confirmed by the lead physician at the admission
- Be affiliated to a social security regime
- Provide informed consent
You will not qualify if you...
- Severe depression, delusion disorder, or substance use disorder
- No access to internet
- Non-French speakers
- Currently participating in another research study on IEI
- Under an exclusion period for another study
- Benefiting from French state aid known as AME
- Deprivation of liberty by court or administrative order
- Hospitalized without consent
- Under protective measures
- Pregnancy and/or breastfeeding
AI-Screening
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Trial Site Locations
Total: 1 location
1
Unité de pathologies professionnelles et environnementales, Hôtel-Dieu
Paris, Paris, France, 75004
Actively Recruiting
Research Team
V
Victor Pitron, MD, PHD
CONTACT
I
Ingrid Zablith
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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