This study aims to evaluate a novel diet for adult Crohn's disease patients (The Crohn's Disease Exclusion Diet - CDED). Some of the patients in this study will receive the CDED combined with partial enteral nutrition (PEN), while the other group will receive the CDED with early introduction of dairy products, that were eliminated from the initial CDED protocol.
Crohn's disease (CD) is a chronic relapsing inflammatory bowel disease that has a significant impact on patients' quality of life and is of increased incidence worldwide. The disease aetiology is complex and not fully understood. Accumulated data indicate that environmental factors, including diet, might play a key role in the pathogenesis and inflammation, through mechanisms involving gut dysbiosis, in genetically susceptible people. Epidemiological data suggest that a Mediterranean dietary pattern is associated with decreased risk for CD, whereas a Western diet, rich in animal fat, processed foods and food additives, seems to be linked with an increased disease risk. Exclusive Enteral Nutrition (EEN) is the only well-established dietary therapy in CD and is used as the first line therapy for the induction of remission in mild to moderate pediatric CD. Evidence according to EEN efficacy in adults is not consistent, which could partly be explained by the compliance difficulty. It is of interest, that feacal inflammation increases rapidly after food re-introduction following EEN in children. Partial enteral nutrition (PEN) has been shown to be beneficial in maintaining remission, but poor compliance due to low formula palatability and patients' fatigue remains an important barrier in the clinical practice. Moreover, PEN is inferior to EEN in inducing remission. Crohn's Disease Exclusion Diet (CDED), which eliminates specific dietary components hypothesized to induce dysbiosis, appears to be effective in inducing and maintaining remission both in pediatric and adult populations. In parallel, patients express a strong interest in ways to manage their disease through diet, so the establishment of a palatable and as flexible as possible dietary pattern, not merely for inducing remission, but also as a feasible maintenance strategy is one of the main priorities in CD research at present. Therefore, the aim of this study is to explore the effectiveness of the CDED and PEN in both inducing and maintaining remission of CD in adults. The investigators also wish to challenge patients with an early exposure to dairy products, to assess tolerability, prospecting for the development of a more flexible dietary approach based on the CDED principles. The investigators aim to assess the intervention effect on CD activity, based on routinely used clinical indices, blood and faecal inflammatory biomarkers (CRP, FC), health-related quality of life, nutritional status and dietary intake, in patients with mildly active CD.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
44
Dietary intervention (Liquid food replacement intervention and specific exclusion diet). Focus on 24 hour diet recalls to asses adherence.
Dietary intervention (Specific exclusion diet plus early dairy introduction). Focus on 24 hour diet recalls to asses adherence.
Evangelismos General Hospital of Athens
Athens, Attica, Greece
Clinical response - Change in Harvey Bradshaw Index (HBI)
Higher HBI scores indicate worse outcomes. Clinical response is defined as baseline HBI score decrease of ≥ 3, and clinical remission is defined as score \<5
Time frame: Baseline, 6 weeks, 12 weeks
Faecal calprotectin
Change in faecal calprotectin level
Time frame: Baseline, 6 weeks, 12 weeks
Change in serum CRP
Abnormal/higher values indicate worse outcomes.
Time frame: Baseline, 6 weeks, 12 weeks
Change in serum Albumin
Abnormal values indicate worse outcomes
Time frame: Baseline, 6 weeks, 12 weeks
Bowel symptoms improvement
Percent of patients who reported improvement in bowel symptoms, assessed by the validated IBDQ (bowel symptoms domain: 10 questions)
Time frame: Baseline, 6 weeks, 12 weeks
Health Related Quality of Life (HR-QoL)
HR-QoL defined by the self-administered Inflammatory Bowel Disease questionnaire (IBDQ) score. Higher IBDQ scores indicate better outcomes. Clinical response defined as increase ≥16 points.
Time frame: Baseline, 6 weeks, 12 weeks
Patient's tolerance to the diet
Intolerance: patient's refusal to continue diet (based on reporting and the 24 hour recalls); Adherence will be assessed based on the modified Medication Adherence Report Scale (MARS) questionnaire; The modified MARS questionnaire rates how closely patients adhere to the diet. A score of 1-5 indicates that the patient is not adherent; a score of 6-9 indicates that the patient is adherent.
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Time frame: Baseline, 6 weeks, 12 weeks
Weight (kg)
Comparison of body weight between the groups.
Time frame: Baseline, 6 weeks, 12 weeks
Body mass index (BMI) (kg/m^2)
Comparison of Body Mass Index (BMI) (kg/m2) between the groups.
Time frame: Baseline, 6 weeks, 12 weeks
Waist circumference (WC) (cm)
Comparison of WC between groups.
Time frame: Baseline, 6 weeks, 12 weeks
Handgrip strength (kg)
Handgrip strength measured with handgrip strength dynamometer
Time frame: Baseline, 6 weeks, 12 weeks
Neck circumference (cm)
Comparison of neck circumference measured with tape measure between the groups
Time frame: Baseline, 6 weeks, 12 weeks
Mid arm circumference (MAC) (cm)
Measured with tape measure to assess Mid-arm muscle circumference (MAMC) (for estimating FFM, when BIA is not feasible)
Time frame: Baseline, 6 weeks, 12 weeks
Triceps Skinfold (TSF) (mm)
Measured with a skinfold caliper to assess Mid-arm muscle circumference (MAMC) for estimating FFM, when BIA in not feasible)
Time frame: Baseline, 6 weeks, 12 weeks