A Culturally Tailored Dietary Intervention to Treat Crohn's Disease
Purpose
The goal of the study is to test the efficacy of a dietary intervention in inducing clinical response and remission for patients with Crohn's disease in a randomized controlled trial. The intervention diet: DAIN has been adapted from the Inflammatory Bowel Disease Anti-Inflammatory Diet or IBD-AID™ taking into account the food availability and preferences of Puerto Ricans. DAIN also includes traditional foods commonly consumed in the typical Puerto Rican diet while maintaining the fundamental components of the IBD-AID™.
Condition
- Crohn Disease
Eligibility
- Eligible Ages
- Between 21 Years and 65 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- 21 to 65 years old - Confirmed CD diagnosis with sCDAI <450 (includes values ranging from remission, mild to moderate activity) - Moderate to severe impaired QoL (sIBDQ<60) - Stable doses of medications are screened; thiopurines, natalizumab, methotrexate (12 weeks), anti-tumor necrosis factor (TNF), ustekinumab, vedolizumab (8 weeks), 5-aminosalicylic acid (5-ASA) (2 weeks), steroids (1 week) - Willingness and capacity to significantly change diet (arm 1) - Willing and able to comply with specimen collection and other study procedures, and to complete the study
Exclusion Criteria
- Ostomy - Use of Specific Carbohydrate Diet of IBD-AID™ within 4 weeks of screening - Use of prescribed probiotics within 4 weeks of screening - > 20mg prednisone or equivalent - Recent C. difficile colitis - Pregnancy - Presence of symptomatic or significant structure or history of obstruction in the past 6 months
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- Randomized intervention trial in adults with Crohn's disease.
- Primary Purpose
- Treatment
- Masking
- Double (Investigator, Outcomes Assessor)
- Masking Description
- All staff collecting data (e.g., dietary assessment) or assaying samples (e.g., fecal calprotectin, cytokines, sequencing) including the PI's, will be blinded to diet group assignments.
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Arm1: Crohn's disease patients + DAIN |
Participants will have 10 weeks of DAIN intervention (From week 1 to week 10) |
|
|
No Intervention Arm 2: Crohn's disease patients no intervention |
Participants will continue consuming their usual diet, with no intervention |
|
Recruiting Locations
More Details
- NCT ID
- NCT05627128
- Status
- Active, not recruiting
- Sponsor
- University of Massachusetts, Worcester
Detailed Description
Crohn's disease is a chronic recurrent inflammatory disorder of the gastrointestinal that results from an inappropriate inflammatory response to an altered gut microbiome (i.e., dysbiosis). Diet is the main driver of microbiome composition. Diet also has been increasingly recognized as a cost-effective strategy to induce remission in pediatric and adult patients with Crohn's disease but diets that can substitute traditional and locally available foods among Puerto Ricans have not been explored. DAIN, a newly created dietary program, incorporates an extensive patient curriculum of recipes and menus adapted to the local availability and food preferences of Puerto Rican patients with Crohn's disease. This study aims to address three questions: whether DAIN a diet adapted to Puerto Rican patients with Crohn's disease, can: 1) induce clinical response and remission; 2) change the inflammatory tone, and 3) revert dysbiosis in Crohn's disease patients. Participants will be randomized 1:1 ratio into two arms: - Arm 1 Crohn's disease patients + DAIN (Experimental): this group of patients will participate in ten weeks of DAIN intervention (From week 1 to week 10) - Arm 2 Crohn's disease patients no intervention (Control): this group of patients will not participate in the DAIN dietary intervention and will continue the usual diet. Participation in the study lasts for 15 weeks with four-time points: week 0 (baseline), week 6, week 10, and week 14. At each time point, all subjects will complete a series of questionnaires to assess overall health, Crohn's disease activity, and dietary compliance. Blood and stool samples will be also collected at home at each time point. Samples will be either shipped or brought to the Research Unit at the Inflammatory Bowel Disease Clinic at the University of Puerto Rico. The primary outcome is Improvement of health-related quality of life. Secondary outcomes are: (i) reduction of inflammation, (ii) changes in the gut microbiome, (iii) clinical response and remission,and (iii) dietary compliance.