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Diet Intervention for Colorectal Cancer Prevention
N/A
Recruiting
Research Sponsored by University of Michigan
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
History of CRC in at least one primary relative or in at least two secondary relatives
Prior resected early-stage CRC (Stage I-IIIA or T1-3, N0-1, M0)
Must not have
Has an infectious disease at the present time.
Has a history of cytotoxic treatment (radiation, chemotherapy) for any type cancer within the last year, except for basal cell or squamous cell tumors of the skin that have been surgically excised and required no further treatment
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change over 12 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing different diets to see which is the most effective in preventing colorectal cancer in people who are overweight or obese.
Who is the study for?
This study is for overweight or obese adults with a history of early-stage colorectal cancer or polyps, or who have a family history of these conditions. Participants should be able to control their diet and not expect major lifestyle changes in the next year. They must also be willing to use an app and receive support calls.
What is being tested?
The MyBestGI study tests three different healthy eating plans over 12 months to see which helps improve diet quality and potentially reduce weight. It includes telephone support, a web-based app, and regular check-ups with body composition measures and blood samples in Ann Arbor.
What are the potential side effects?
There are no direct side effects from participating as this trial involves dietary interventions rather than medication. However, changes in diet can affect individuals differently; some may experience digestive adjustments or need medication dosage changes if they manage other conditions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
One of my close family members or at least two distant relatives had colorectal cancer.
Select...
I had surgery for early-stage colorectal cancer.
Select...
I have a genetic condition that raises my risk for colorectal cancer.
Select...
I agree to possibly follow a special diet plan or continue my usual care.
Select...
I have had a type of polyp called adenomatous before.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I currently have an infectious disease.
Select...
I haven't had cancer treatment in the last year, except for minor skin cancer surgery.
Select...
I am not pregnant, breastfeeding, nor planning to become pregnant during the study.
Select...
I cannot make my own daily food choices.
Select...
I am on blood thinners that may affect blood sampling.
Select...
I am unable to understand and agree to the study's procedures and risks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change over 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change over 12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Preventive Food Score
Weight Loss
Other study objectives
Breath Ketone Concentration
Skin Carotenoids
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Eating Plan 3Experimental Treatment1 Intervention
This group will receive a version of the MyBestGI App and User Manual that encourages meeting 11 food group goals: four food groups to limit and seven food groups to encourage. The 7 groups to encourage are: 3-4 cups/day fruits and vegetables, at least one dark orange or dark green vegetable daily, daily allium and culinary herbs, 3-6 oz./day whole grains, 6-8 oz./week foods high in omega-3 fatty acids, 8-10 tsp./day olive oil or the equivalent from other foods high in monounsaturated fats and at least ½ cup/day of legumes or 1 TB/day nut butter. Some of the goals are personalized based on calculated energy needs. They will also receive the results of their own breath test, Veggie Meter score and anthropometric measures.
Group II: Eating Plan 2Experimental Treatment1 Intervention
This group will receive the MyBestGI App and User Manual that encourages limiting four food groups: three or less foods each day made with refined flour, no more than 8% of calories from added sugars, no processed meats and less than 18 oz./week red meat. They will also receive the results of their own breath test, Veggie Meter score and anthropometric measures.
Group III: Eating Plan 1Active Control1 Intervention
This group will receive a pamphlet from the American Institute for Cancer Research (AICR) on dietary prevention and the results of their own breath test, Veggie Meter score and anthropometric measures.
Find a Location
Who is running the clinical trial?
University of MichiganLead Sponsor
1,852 Previous Clinical Trials
6,432,502 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,917 Previous Clinical Trials
41,014,227 Total Patients Enrolled
Zora Djuric, PhDStudy ChairUniversity of Michigan
5 Previous Clinical Trials
374 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I currently have an infectious disease.I can be reached by phone for study-related calls.I am at an increased risk for colorectal cancer.I am 19 years old or older.You are able to make healthy choices about what you eat.I haven't had cancer treatment in the last year, except for minor skin cancer surgery.One of my close family members or at least two distant relatives had colorectal cancer.Your diet is lacking important nutrients and relies heavily on alcohol for calories.I had surgery for early-stage colorectal cancer.I have a genetic condition that raises my risk for colorectal cancer.You can eat foods that have a lot of fiber in them.You have reported eating habits that are very strange or not believable.I agree to possibly follow a special diet plan or continue my usual care.I have had a type of polyp called adenomatous before.I am not pregnant, breastfeeding, nor planning to become pregnant during the study.I cannot make my own daily food choices.I am willing to consult my doctor to adjust my medication if my diet changes.I am on blood thinners that may affect blood sampling.I am unable to understand and agree to the study's procedures and risks.I am in good health overall.
Research Study Groups:
This trial has the following groups:- Group 1: Eating Plan 1
- Group 2: Eating Plan 2
- Group 3: Eating Plan 3
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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