Actively Recruiting
Behavioral Therapy for Crohn's Disease
Led by Icahn School of Medicine at Mount Sinai · Updated on 2025-11-20
170
Participants Needed
2
Research Sites
195 weeks
Total Duration
On this page
Sponsors
I
Icahn School of Medicine at Mount Sinai
Lead Sponsor
T
The Leona M. and Harry B. Helmsley Charitable Trust
Collaborating Sponsor
AI-Summary
What this Trial Is About
People living with Crohn's disease (CD) experience psychological and emotional symptoms, in addition to known chronic and disabling physical symptoms, which prevent them from living their life to the fullest (flourishing). Depression and anxiety are experienced by 30% of people living with CD and 60% of inflammatory bowel disease (IBD) patients continue to report chronic pain, stress, sleeplessness, and fatigue, even when they are "objectively" in remission. Psychological stress has been endorsed by 70% of patients with IBD as a key trigger for disease activity which is not surprising given the significance of the gut-brain-microbiome axis, the close communication between the enteric and autonomic nervous systems, and the role of the hypothalamic-pituitary axis and its neuroendocrine and immune functions in the expression of GI symptoms. Interestingly, up to 85% of patients with CD also endorse the positive impact of effective coping skills on disease course. The PI's prior work has suggested that early provision of effective coping strategies, offered at the time of diagnosis or more precisely, immediately prior to biologic medication initiation, could potentially result in faster healing and improved well-being, likely through the combination of 1) physiological mitigation of the stress response and optimization of the gut-brain-microbiome axis; and 2) promotion of effective coping and disease self-management behaviors that promote psychological flourishing despite disease. Unfortunately, to date, early effective psychosocial care has been limited by concerns over reimbursement for psychological services, access to qualified IBD mental health professionals, and the lack of a standardized methodology focused on the brain-gut stress response and how to assess, monitor, communicate and maintain tight control over both physical and emotional well-being. CATHARSIS is a rigorous, placebo-controlled, randomized controlled trial of coping strategies plus medication for 170 people living with Crohn's for less than 5 years who are about to start a new biologic medication due to active disease. Outcomes include improvements in emotional well-being as well as clinical and endoscopic remission over a 12-month period. The overall goal of the study is to demonstrate that it is essential to combine biologic therapy and psychosocial care to ensure optimal and long-term positive outcomes in CD.
CONDITIONS
Official Title
Behavioral Therapy for Crohn's Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 to 65 years old of any sex, gender, and racial or ethnic background
- Confirmed Crohn's disease diagnosis by endoscopy and biopsy
- Active Crohn's disease symptoms with Crohn's Disease Activity Index of at least 220
- Active endoscopic inflammation or evidence of active disease by imaging or elevated biomarkers
- Planning to start or have started anti-TNF or anti-IL-23 biologic medication within 2 weeks before or 6 weeks after enrollment
- Must live in one of Dr Keefer's 30+ PSYPACT licensed states
You will not qualify if you...
- Endoscopically inactive Crohn's disease at the start of the study
- Unable to provide consent for participation
- Pregnant or planning pregnancy within the next 12 months
- Severe psychiatric symptoms
- History of surgery for Crohn's disease
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Icahn School of Medicine at Mount Sinai
New York, New York, United States, 10029
Actively Recruiting
2
New York Gastroenterology Associates
New York, New York, United States, 10128
Actively Recruiting
Research Team
L
Laurie Keefer, PhD
CONTACT
C
Candela De Amorrortu
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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