Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Fred Hutchinson Cancer Center
With
National Cancer Institute (NCI)
Participants are randomized to 1 of 2 groups.
GROUP I (INTERVENTION GROUP): Participants eat a diet consisting of resistant starch foods daily for 8 weeks. Study provided foods are in addition to their own usual daily diet.
GROUP II (CONTROL GROUP): Participants eat a diet consisting of regular corn starch foods daily for 8 weeks. Study provided foods are in addition to their own usual daily diet.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
History of diagnosed American Joint Committee on Cancer (AJCC) stage I-III colorectal adenocarcinoma.
Completed all treatment of colorectal adenocarcinoma within past 4-36 months.
Current Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 (per physician).
Ability to consent and follow study protocol.
You may not be if
Active cancer.
Prior diagnosis of diabetes that is currently uncontrolled (defined as hemoglobin \[Hgb\] A1c \> 8.0).
Active inflammatory bowel disease (i.e., patients who are symptomatic despite medical therapy). This includes irritable bowel syndrome, Crohn's disease, or any other inflammatory bowel disorder.
Known food allergy/intolerances to wheat, gluten, dairy or eggs.
Use of antibiotic(s) within the last 3 months prior to enrollment.
