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Nutritional Therapy Study in Pediatric Crohn's Disease

Primary Purpose

Crohn's Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Traditional SCD Diet
Modified SCD Diet
Whole foods diet
Sponsored by
Seattle Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn's Disease focused on measuring Specific Carbohydrate Diet, Diet, Nutrition

Eligibility Criteria

12 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Children and adolescents 8 to 21 years old
  2. Diagnosis of Crohn's Disease made by a primary gastroenterologist based upon history, physical exam, laboratory/radiological studies and gastrointestinal histology
  3. Mild or moderate disease activity based upon PCDAI score (10-45)
  4. Parent/guardian and child must be able to comprehend the consent and assent
  5. Parent/guardian and participant must be able to attend study visits at baseline, and weeks +2, +4, +8, +12.
  6. Patient must not have medication changes for his/her inflammatory bowel disease medications for at least 1 months, unless medically necessary.

Exclusion Criteria:

  1. Severe disease with PCDAI >45
  2. Active or history of intra abdominal abscess, intra abdominal fistula, stricturing Crohn's disease
  3. Other serious medical conditions such as neurological, liver, kidney, autoimmune or systemic disease.
  4. Has begun TNF inhibitors within two months prior to study
  5. Has had change of maintenance medication within the last month
  6. Tobacco, alcohol or illicit drug abuse
  7. Pregnant subject recipients will be excluded

Sites / Locations

  • Seattle Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Traditional SCD Diet

Modified SCD Diet

Whole Foods Diet

Arm Description

7 subjects will be randomized to a traditional SCD diet

7 subjects will be randomized to a "modified SCD diet", which includes oatmeal and rice

7 subjects will be randomized to a" Whole foods diet" without added sugars

Outcomes

Primary Outcome Measures

Change in Pediatric Crohn's Disease Activity Index
Activity Index is a validated form of measurement for disease activity

Secondary Outcome Measures

Fecal Microbiome Analysis
Changes in fecal microbiome as defined by species types and percent of total microbiome will be measured using Metagenomic Phylogenetic Analysis (MetaPhlAn)
Change in C-reactive protein at Baseline and 12 weeks
Decrease in C-reactive protein (CRP) by Immunorate by Vitros 4600
Change in Calprotectin at Baseline and 12 weeks
Decrease in fecal calprotectin by ELISA

Full Information

First Posted
November 16, 2015
Last Updated
May 22, 2019
Sponsor
Seattle Children's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02610101
Brief Title
Nutritional Therapy Study in Pediatric Crohn's Disease
Official Title
A Blinded, Nutritional Therapy Study, Using a Modified Specific Carbohydrate Diet in Pediatric Crohn's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seattle Children's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators are doing this research study to answer questions about a nutritional therapy called the Specific Carbohydrate Diet (SCD) for children with active Crohn's Disease (CD). The SCDiet is a diet where all grains such as wheat, barley, corn, rice are restricted. Most dairy products (except certain yogurt) are also restricted. The diet mainly consists of meat, fruits, vegetables, nuts, oils and honey, and is offered to individuals with active Crohn's disease as part of standard of care at Seattle Children's. For this study, the investigators will have three different dietary groups: Traditional SCD diet group Modified SCD to include oatmeal and rice SCD with whole foods without added sugar Specifically, the investigators want to know: Is the SCD well tolerated? Is SCD effective for the treatment for active Crohn's Disease? Will the results from the varied three dietary groups have the same results for each patient?
Detailed Description
21 patients with CD , mild or moderate disease activity as defined by Pediatric Crohn's disease activity index (PCDAI score of 10-45 ) aged 8 -21 years will enroll into this study.Patient's will be randomized to treatment groups. The treatments for this study will be the:(1) Standard SCD as defined by Elaine Gottschall's Breaking the vicious cycle (2) Modified SCD with added oats and rice (3) Whole foods diet without added sugars. Each patient will receive an initial evaluation including a physical exam, medication review, nutritional guidance and post treatment evaluations. Initial evaluation: Study subject recipient will have the following lab tests including CBC with differential & platelets, a c-reactive protein, sedimentation rate, an albumin, vitamin D level,Cholesterol, Vitamin A, Vitamin E, Zinc, Folate, a stool study for c. difficile, for bacterial culture and ova and parasite, stool calprotectin and microbiome. Additionally, the investigators will complete a physical exam and document their current medications. The study nutritionist will complete a thorough diet history. Treatment: Patient's will be randomized to treatment groups. The treatments for this study will be the:(1) Standard SCD as defined by Elaine Gottschall's Breaking the vicious cycle (2) Modified SCD with added oats and rice (3) Whole foods diet without added sugars Families will be given a list of "safe foods" that the patient can eat no matter which group the patient is in. Food will be prepared by a Chef knowledgeable in the SCD and whole food diets. Recipes will be predetermined and families will be able to decide food for patient based upon menus. Patients will receive one-on-one guidance by a Seattle Children's Dietician trained in the SCD during each visit. Prior to each visit patient will fill out a 3 day nutrition log which will be reviewed by the dietician during the clinic visit. Follow-up: Each study subject will have clinical follow-up at 2 weeks, 4 weeks, 8 weeks and 12weeks. Standardized questionnaires, including the Pediatric Crohn's disease activity index (PCDAI) will be completed during each study visit. Information about tabulating the PCDAI scores, is listed in Appendix A. In addition patients will have a physical exam and standard blood work including CBC, sedimentation rate, C-reactive protein, albumin and stool for microbiome analysis at each follow up visit. This stool will be sent to the University of Washington (Dr. Sam Miller's lab) for analysis;additional stool samples will be sent to Katrine Whitson at UC Irvine for protein analysis. Stool calprotectin will additionally be done at week 4 and 12. Vitamin D level will be measured at week 12. Finally, all patients will meet with the nutritionist at each visit who will complete a thorough diet review. Any questions about the SCD will be addressed at each visit. All study related information will be stored in the RedCap database. Participant data for the study will be stored electronically in the REDCap platform. The REDCap platform is managed by the Institute for Clinical and Translational Science at the University of Washington. Only IRB approved research team members will have access to the REDCap data platform. Each team member will be granted access to the REDCap data system through a secure login. The information about each participant will be de-identified using a unique study code. Some personal information such as date of birth will be stored in RedCap. Microbiome: Some stool from the participants at screening, week 2, 4, 8 and 12 will be stored for microbiome analysis. The samples will be stored at Seattle Children's Hospital in the Clinical Research Center lab in the -80 freezer. These samples will be sent to the University of Washington for microbiome analysis and storage on an as necessary basis. Each of these samples will be de-identified and labeled with a unique study code and visit number. Consent for storage will be part of the Informed Consent process.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease
Keywords
Specific Carbohydrate Diet, Diet, Nutrition

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Traditional SCD Diet
Arm Type
Active Comparator
Arm Description
7 subjects will be randomized to a traditional SCD diet
Arm Title
Modified SCD Diet
Arm Type
Active Comparator
Arm Description
7 subjects will be randomized to a "modified SCD diet", which includes oatmeal and rice
Arm Title
Whole Foods Diet
Arm Type
Active Comparator
Arm Description
7 subjects will be randomized to a" Whole foods diet" without added sugars
Intervention Type
Other
Intervention Name(s)
Traditional SCD Diet
Other Intervention Name(s)
SCD
Intervention Description
Traditional SCD includes removal of all processed foods as well as all grains, sweetners except for honey and all diary except for yogurt fermented for over 24hrs and some hard cheeses
Intervention Type
Other
Intervention Name(s)
Modified SCD Diet
Other Intervention Name(s)
Modified SCD
Intervention Description
Food components of the traditional SCD with the addition of rice and oats.
Intervention Type
Other
Intervention Name(s)
Whole foods diet
Intervention Description
A whole foods diet with removal of processed foods. Removal of corn, wheat, sugar and milk are also apart of this dietary regime.
Primary Outcome Measure Information:
Title
Change in Pediatric Crohn's Disease Activity Index
Description
Activity Index is a validated form of measurement for disease activity
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Fecal Microbiome Analysis
Description
Changes in fecal microbiome as defined by species types and percent of total microbiome will be measured using Metagenomic Phylogenetic Analysis (MetaPhlAn)
Time Frame
12 weeks
Title
Change in C-reactive protein at Baseline and 12 weeks
Description
Decrease in C-reactive protein (CRP) by Immunorate by Vitros 4600
Time Frame
12 weeks
Title
Change in Calprotectin at Baseline and 12 weeks
Description
Decrease in fecal calprotectin by ELISA
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children and adolescents 8 to 21 years old Diagnosis of Crohn's Disease made by a primary gastroenterologist based upon history, physical exam, laboratory/radiological studies and gastrointestinal histology Mild or moderate disease activity based upon PCDAI score (10-45) Parent/guardian and child must be able to comprehend the consent and assent Parent/guardian and participant must be able to attend study visits at baseline, and weeks +2, +4, +8, +12. Patient must not have medication changes for his/her inflammatory bowel disease medications for at least 1 months, unless medically necessary. Exclusion Criteria: Severe disease with PCDAI >45 Active or history of intra abdominal abscess, intra abdominal fistula, stricturing Crohn's disease Other serious medical conditions such as neurological, liver, kidney, autoimmune or systemic disease. Has begun TNF inhibitors within two months prior to study Has had change of maintenance medication within the last month Tobacco, alcohol or illicit drug abuse Pregnant subject recipients will be excluded
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David L Suskind, MD
Organizational Affiliation
Seattle Children's Hospital and The University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
Seattle Children's Hospital
City
Seattle
State/Province
Washington
ZIP/Postal Code
98105
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Undecided
Citations:
PubMed Identifier
24048168
Citation
Suskind DL, Wahbeh G, Gregory N, Vendettuoli H, Christie D. Nutritional therapy in pediatric Crohn disease: the specific carbohydrate diet. J Pediatr Gastroenterol Nutr. 2014 Jan;58(1):87-91. doi: 10.1097/MPG.0000000000000103.
Results Reference
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Nutritional Therapy Study in Pediatric Crohn's Disease

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