CD-TREAT Diet: a Novel Therapy for Active Luminal Crohn's Disease

Children and adults who are eligible to participate will be identified by medical staff. A member of the clinical team will briefly inform potential participants about the study via the phone, via e-mail, or at the clinic. After the end of the clinical appointment and if the patient and/or the parent/carer are agreeable, a member of the clinical team will introduce the eligible participants to the researcher who will explain the study in full and answer any questions they might have. During this meeting, the researcher will discuss the specific aspects of dietary treatment with CD-TREAT and will inform participants that urine, blood and faecal samples will be collected to try and determine the type of bacteria which may be associated with gut inflammation, and their metabolites, and whether these can predict response to treatment. The researcher will also ask for permission to collect medical information from the participant's medical records. If they are interested in taking part, they will be given detailed written information (including an age-appropriate information leaflet). The information pack will also invite the family to contact the researcher at any time if they require further information.

As there is a very narrow time window between identification of eligible participants and consent to participate to the study, and considering the need for immediate initiation of treatment in patients with active disease, it is anticipated that signed consent to join the study will be obtained on the same day of receiving information about it; however there will be subsequent opportunity to review this decision. Consent will only be taken if participants feel they have had adequate time to make this decision, and no pressure will be applied in any way.

This will also facilitate the completion of a health check questionnaire, baseline clinical review, medication and disease history, quality of life assessment, anthropometry measurements, collection of baseline research bloods (extra volume at the time of routine clinical tests (no additional venepuncture required). At this point the participant will be asked to take a stool and urine sample collection kit at home and a suitable date/time to collect the baseline samples will be arranged. The actual intervention will start approximately 24 hours later in order to allow the participants enough time to consider and discuss the study with their relatives, decide whether they would like to continue or drop out and start the standard induction treatment as deemed necessary by the treating clinical team. Furthermore, this 24 hour time window will enable the researcher to collect baseline samples before the initiation of the CD-TREAT dietary treatment.

Where appropriate, the assent of the child will be sought (usually under age 11 or younger), and in the case of young adults who would be deemed able by a member of the clinical team to consent on their own part (usually age 12 or older), consent from the young person will be accompanied by the parent/carer giving signed assent before they can join the study; to ensure both child and parent/carer are willing and happy to take part. For children unable to give written consent/assent, the parent/carer will be asked to explain the study in terms that the child can understand and the carer will sign consent on their behalf.

It will also be made clear at this stage, on information sheets and throughout the study that participants can withdraw from the study at any time without it affecting their routine care in any way. Continuation of CD-TREAT dietary advice and provision of CD-TREAT foodstuffs is dependent however on continuation in the study. Discontinuation of study participation after commencement of CD-TREAT would therefore involve return to standard induction treatment at the discretion of the treating clinical team.

Throughout the study recruited participants will be asked to provide urine, faecal and blood samples (an additional small tube of blood when they are having routine bloods at clinical appointments) on a maximum of 4 occasions. In addition, these time points will include clinical review, quality of life assessment and anthropometry measurements.

Participants will also provide some dietary information reflecting their compliance to CD-TREAT diet.

CD-TREAT Intervention:

All patients on the CD-TREAT diet will be supplied with an individually tailored, dietitian-devised diet, consisting of ordinary foods, but custom-designed to recreate the nutritional content and ingredients of EEN. The dietary intervention will be overseen by qualified dieticians including a National Health Service (NHS) research dietician. The energy content will be tailored to adult participants' total energy expenditure and physical activity level calculated by the World Health Organisation (WHO) set of equations or will be calculated for each child to meet their estimated average requirement (EAR) for age. Food and instructions for those patients on CD-TREAT will be supplied directly to them by the researchers on the day following recruitment. Foods which need cooking will be prepared by a sub-contracted (food handling and hygiene certified) catering company and will be delivered to the participants' house every 2-3 days. The rest of the foods will be delivered to the participants' house every week. Participants will initially receive the modified diet for a period of 8 weeks, similar to the duration of an EEN course. The researchers will instruct the participants and their carers on how to follow the diet and how to record their dietary intake during the intervention. Research follow-up visits will coincide with the participants' clinical follow-ups (Week 2: phone review; Weeks 4 \& 8: hospital visit). These follow up appointments will include collection of research bloods as an extra aliquot to their routine clinical tests (no additional needle insertion is required), clinical review, quality of life assessment and anthropometry measurements. At these appointments, the researchers will give the participants a stool and urine sample collection kit to take home and will arrange a suitable date/time to collect the faecal and urine sample.

Response to treatment will be assessed according to clinical review, CD activity score and measurements of established biomarkers in faeces and blood (e.g. faecal calprotectin). The primary endpoint will be clinical response (Adults: HBI fall≥3; Children: wPCDAI fall≥17.5) or clinical remission (Adults: HBI<5; Children: wPCDAI<12.5) at 8 weeks; while secondary endpoints include reduction in faecal calprotectin and blood inflammatory markers and changes in anthropometry. All patients will be under close follow-up. No new CD-related medications will be allowed during the pilot study, however if patients' disease activity is deteriorating at any point during the study or there is no response at 4 weeks, patients will be eligible to discontinue CD-TREAT diet and commence medical/surgical treatment as deemed necessary by the treating clinical team. Those participants will still be encouraged to provide stool, blood and urine samples at intervention exit. For those demonstrating response, all background CD-related medication dosages will remain stable unless a subject develops specific drug-related side-effects, blood monitoring abnormalities or blood drug levels requiring alteration. Those patients who experience clinical response but not clinical remission at 8 weeks will be given the opportunity to stay on CD-TREAT for a further 4 weeks. At the end of this period (12 weeks post CD-TREAT initiation) they will be asked to provide the last stool and urine sample and they will have the last follow-up appointment including collection of research bloods, clinical review, quality of life assessment and anthropometry measurements.