Personalized "Alberta" Diet for Prevention of Relapse in Ulcerative Colitis

Ulcerative Colitis Clinical Trial

Official title:

A Dietary Approach to Reduce the Frequency of Relapse in Ulcerative Colitis Patients: a Randomized Controlled Clinical Trial Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02093780
• Other study ID #: Pro00035413
• Status: Completed
• Phase: N/A
• Start date: March 2014
• Est. completion date: October 2017

Study information

• Verified date: April 2018
• Source: University of Alberta
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In the present study, ulcerative colitis (UC) patients in the remission stage of the disease will be randomized into two groups: Alberta anti-inflammatory diet and Canada's Food Guide diet. The elements of Alberta anti-inflammatory diet have previously been shown to have a role in decreasing the risk of UC development or management of UC-related symptoms or relapse. Since the primary outcome of interest is the relapse rate in two groups, disease status will be assessed monthly using appropriate tools. In order to find out the underlying mechanisms that will relate the proposed diet to decreased flare rate, some laboratory evaluations, which are mainly markers of inflammation or are related to gut microbiome will be conducted. In the present study, the investigators will also perform state-of-the art metabolomics tests, in order to study how the dietary changes will change the end metabolites. In addition, the investigators will be able to explore if metabolomic profile of participants can predict future UC relapse. This study will last for 6 months from baseline wherein all the study subjects will receive appropriate dietary instructions in addition to their stable doses of maintenance drug therapy.

Description:

Recent research suggests that habitual dietary may play an important part in the treatment of inflammatory bowel disease (IBD), but this has not been systematically explored. Habitual intake of a diet that is rich in "anti-inflammatory" nutrients (e.g. n-3 fatty acids, polyphenols), soluble fiber and other prebiotics (e.g. inulin), and probiotics (that improve gut microbiota) may lead to major improvements in IBD disease. Ultimately, the investigators are interested in studying the extent to which habitually eating foods, sources of these important nutrients and dietary components, might help people with IBD living in Alberta. Thus, the information about nutrients and dietary components must be translated to foods and dietary patterns that are acceptable and accessible to people in Alberta. This study will compare the effectiveness of 2 different approaches, either a structured, personalized menu plan constructed with a dietitian (intervention group) vs. general advice to follow Canada's Food Guide by a dietitian (control group), to promoting uptake and adherence to an appropriate diet. The control group will receive the same care as the intervention group as far as access to a registered dietitian. In the intervention group, the nutritional advice offered will be to follow a structured four-week menu plan that includes recipes and nutrition tips. The menu plan emphasizes specific foods that have been shown in the literature to improve IBD symptoms. In the control group, the nutritional advice will be general and will emphasize the principles outlined in Canada's Food Guide. Each control participant will be provided with their daily serving size allowance for each of the four food groups. Each participant will have sole responsibility in deciding which foods are selected from each food group; specific foods will not be highlighted.

Objectives: To evaluate if the proposed Alberta anti-inflammatory diet is effective for the prevention of relapses in ulcerative colitis as well as to determine their protective mechanisms

Study Design: Randomized controlled clinical trial Study Population and Number of Subjects:

70 patients with ulcerative colitis in clinical remission Duration of Treatment: 6 months Primary Endpoint: Patient relapse rate over 6 months Secondary Endpoints: Changes in: 1) Time to relapse; 2) Patients' quality of life during the study period; 3) Mucosal inflammation, measured by fecal calprotectin at baseline, months 1, 3, 6 or at relapse; 4) Partial Mayo score at the baseline and monthly, or at a relapse; 5) Laboratory markers of inflammation

Subject visits:

1. Screening Visit

• Assessment of inclusion of exclusion criteria

• Obtainment of Informed Consent

• Medical History

• Pregnancy Test

• Partial Mayo score

2. Visit Month 0 (baseline), 1, 3, 6 (or at relapse)

• Focused Physical Exam and Medical History

• Partial Mayo score

• Fecal samples for Calprotectin and luminal microflora analysis

• Blood and urine samples for metabolomic analysis, inflammatory markers and other tests specified in the appendix 2.

• Dietary counseling

• Questionnaires specified in the appendix 2.

• Sigmoidoscopy (only at relapse)

3. Visit at Month 2, 4, 5

• Telephone interview by the dietician

• Partial mayo score

• Questionnaires specified in the appendix 2

Studies to Evaluate Mechanisms of Action of the Alberta anti-inflammatory diet:

• Compositional changes of the intestinal microbiota in fecal samples, using pyrosequencing

• Host and microbial metabolomics in serum and urine samples using gas chromatography and nuclear magnetic resonance

• Evaluations of inflammatory markers (fecal calprotectin, serum interleukin (IL) -6, C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and lipopolysaccharide (LPS).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 53
• Est. completion date: October 2017
• Est. primary completion date: October 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Participants must have Ulcerative Colitis in clinical remission (partial Mayo score of less than 2)

• Fecal calprotectin of more than 150 microgram/g

• Patients on oral 5-ASA drugs and/or Azathioprine or 6-mercaptopurine as long as the dose has been stable for 2 weeks (between 2-2.4 gram daily for oral 5-ASA) or 2 months (for azathioprine or 6-mercaptopurine).

• Participants must be generally healthy besides having UC

• Must be able to communicate in English.

• Live in the Edmonton Area.

Exclusion Criteria:

• Use of prednisone (or steroid equivalent) at the time of enrollment.

• Use of anti-TNF drugs within 3 months of enrollment.

• Use of antibiotics (washout period of at least 2 weeks is required).

• Pregnancy or lactation.

• History of colectomy.

• Significant chronic disorders such as severe cardiac disease, significant renal failure, severe pulmonary disease (need for oxygen).

• Active gastrointestinal infection.

• Severe psychiatric disorder.

• Unable or unwilling to consent

Related Conditions & MeSH terms

• Colitis
• Colitis, Ulcerative
• Ulcer
• Ulcerative Colitis

Intervention

Behavioral:
• Alberta Anti-inflammatory diet
Patients randomized to Alberta Anti-inflammatory diet will follow a strict menu plan designed by certified dietitian for 6 months.
• Canada's Food Guide Diet
Patients randomized to Canada's Food Guide diet will receive counseling by certified dietitian for 6 months and will design their own diet following Canada's Food Guide.

Locations

Country	Name	City	State
Canada	University of Alberta	Edmonton	Alberta

Sponsors (1)

Lead Sponsor	Collaborator
University of Alberta

Country where clinical trial is conducted

Canada, 

References & Publications (2)

Olendzki BC, Silverstein TD, Persuitte GM, Ma Y, Baldwin KR, Cave D. An anti-inflammatory diet as treatment for inflammatory bowel disease: a case series report. Nutr J. 2014 Jan 16;13:5. doi: 10.1186/1475-2891-13-5. — View Citation

Richman E, Rhodes JM. Review article: evidence-based dietary advice for patients with inflammatory bowel disease. Aliment Pharmacol Ther. 2013 Nov;38(10):1156-71. doi: 10.1111/apt.12500. Epub 2013 Sep 17. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient relapse rate	Relapse is defined as the total partial Mayo score exceeds 2. Partial Mayo score represents a sum of the subject's symptoms for rectal bleeding and stool frequency, as well as a physician global assessment score, each of them scored from 0 to 3.	6 months
Secondary	Time to relapse	Time from start until clinical relapse (outcome 1)	6 months
Secondary	Quality of Life improvement	Improvement of Quality of Life	6 months
Secondary	change in mucosal inflammation, measured by fecal calprotectin	Mucosal inflammation, measured by fecal calprotectin at baseline, months 1, 3, 6 or at relapse	6 months
Secondary	changes in partial Mayo score from baseline	Partial Mayo disease activity score at the baseline and monthly, and at a relapse	6 months