The ADDapt Diet in Reducing Crohn's Disease Inflammation

King's College London

Status: Active, not recruiting

Conditions: Inflammatory Bowel Diseases; Crohn Disease

Treatments: Behavioral: Dietary education

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04046913

IRAS 260196

Details and patient eligibility

About

Crohn's disease (CD) results in chronic intestinal inflammation, is of increasing incidence both in the developed and developing world and has a marked impact on patient quality of life. The prevalence of CD is 10.6 per 100,000 people in the UK and represents a significant annual financial burden of around €16.7 billion in Europe.

A wide range of nutrients and food components have been investigated for their role in the pathogenesis and course of CD. A common theme suggests that CD risk is associated with a "Western diet", including high fat, high sugar and processed foods. However, intervention studies that exclude specific aspects of the diet such as sugar or that compare low and high fat diets have failed to show effectiveness in practice. Observational human and experimental animal studies suggest that certain food additives used extensively by the food industry play a role in the pathogenesis and natural history of CD. However, to date no evidence exists for the effectiveness of a diet low in these food additives in CD.

Therefore, the aim of this study is to investigate the effects of a diet low in certain food additives compared to a normal UK diet on CD activity, health-related quality of life, gut bacteria, gut permeability, gut inflammation and dietary intake, in patients with mildly active, stable CD. We will recruit patients with mildly active CD and will randomise them to receive either the diet low in the food additives of interest, or the diet representative of a normal UK diet. Patients will follow their allocation diet for 8 weeks and will attend study visits at the start and end of the trial, at which points questionnaires will be completed and samples will be collected.

Enrollment: 154 patients

Sex: All

Ages: 16+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adults aged ≥16 years

• CD diagnosis (defined by standard clinical, histological and radiological criteria) of at least 3 months

• Mildly active disease as defined by:

  • Defined by physician assessment that no change in medication is required
  • Faecal calprotectin >150 µg/g OR endoscopic evidence of active luminal disease OR radiological evidence of active luminal disease (by magnetic resonance enterography, or ultrasound) within the last 8 weeks.
  • CDAI between 150-250

• Current body weight of ≥50 kg

• Individuals able to give informed consent and willingness to participate

Exclusion criteria

• Changes in dose to azathioprine, 6-mercaptopurine, methotrexate or anti-TNF-α agents or other biologics during the preceding 8 weeks, oral 5-ASA during the preceding four weeks. Currently receiving oral prednisolone/budesonide or discontinued within the last 4 weeks, unless they are on a stable dose of 10 mg/day or less prednisolone (3 mg or less budesonide) for at least 4 weeks with the intention to continue this long term.

• Used rectal 5-ASA or rectal steroids in the preceding 4 weeks

• Previous extensive bowel resection, defined as having had >2 intestinal resections, a sub-total colectomy or documented short bowel syndrome

• Poorly controlled bile acid malabsorption

• Current stoma

• Recent use of the following treatments: antibiotics, probiotics, prebiotic or fibre supplements in the preceding four weeks, NSAIDs during the preceding week

• Full bowel preparation for a diagnostic procedure in preceding 4 weeks

• Comorbidities including sepsis/fever, diabetes or coeliac disease, or other concomitant serious comorbidity e.g. significant psychiatric, hepatic, renal, endocrine, respiratory, neurological or cardiovascular disease

• Exclusive enteral nutrition in the past 8 weeks

• Assessed as at nutritional risk, as defined by any of the following:

  • BMI ≤18.5 kg/m2
  • Previous or current eating disorder
  • Currently receiving prescribed oral nutritional supplements

• Following a restrictive diet (e.g. multiple restrictions due to numerous self-reported allergies) as judged by the dietitian

• Reported pregnancy or lactation

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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154 participants in 2 patient groups, including a placebo group

Low food additive diet

Active Comparator group

Description:

Dietary advice, given by a dietitian, will be discussed at trial baseline.

Treatment:

Behavioral: Dietary education

Habitual food additive diet

Placebo Comparator group

Description:

Dietary advice, given by a dietitian, will be discussed at trial baseline.

Treatment:

Behavioral: Dietary education