Rectal Cancer Clinical Trial
Official title:
A Randomized High-Fermented Food Intervention Among Locally Advanced Rectal Cancer Patients (The FEED Trial)
NCT number | NCT06337552 |
Other study ID # | MCC-22709 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | February 19, 2024 |
Est. completion date | March 2027 |
The purpose of the study is to evaluate the feasibility and acceptability of a dietary intervention (FEED-FF) that includes fermented foods (FF), among locally advanced rectal cancer patients, and to explore whether this diet can improve outcomes in rectal cancer patients receiving chemoradiotherapy (CRT).
Status | Recruiting |
Enrollment | 30 |
Est. completion date | March 2027 |
Est. primary completion date | March 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - 18 years of age or older - Diagnosed with locally advanced rectal cancer (Stage II-III) - Receiving neoadjuvant chemoradiation at Moffitt Cancer Center - Able to pick up FFs once/weekly at the PEARL research kitchen - Able to speak and read English - Able to consume foods orally - Able to provide informed consent Exclusion Criteria: - Antibiotic use within 1 month prior to baseline - If currently using probiotics, unwillingness to cease probiotic use - Previous receipt of surgery, immunotherapy, chemotherapy, or radiation for a colon or rectal tumor - Inflammatory bowel conditions (e.g., ulcerative colitis, Crohn's disease) - Immunosuppressive or autoimmune conditions (e.g., lupus, Graves disease, rheumatoid arthritis, psoriasis) - Infectious disease diagnosed <1 month prior to baseline - Already consuming =2 servings of fermented foods/day - Previously diagnosed with a mast cell disorder or histamine allergy |
Country | Name | City | State |
---|---|---|---|
United States | Moffitt Cancer Center | Tampa | Florida |
Lead Sponsor | Collaborator |
---|---|
H. Lee Moffitt Cancer Center and Research Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effects of the FEED-FF diet on clinical response to chemoradiation | Clinical response measured in clinic by MRI/Endoscopy/Digital rectal exam, comparing the FEED-FF arm to SUC arm.
Indicators of clinical response are Complete Response, Near Complete Response, Incomplete Response, or Progressive Disease. |
At Baseline and Up to 12.5 Weeks | |
Primary | Effects of FEED-FF diet on the gut microbiome | Measured by fecal biospecimen sample collection; FEED-FF arm hypothesized to demonstrate increases in short chain fatty acid (SCFA) producing bacteria and higher alpha diversity compared to SUC arm. | At Baseline, Week 6.5 and Up to 12.5 Weeks | |
Primary | Effects of FEED-FF diet on local immune-related biomarkers | Measured by FFPE tissue slides; FEED-FF arm hypothesized to demonstrate enhanced immune response such as higher T-cell expression compared to SUC arm. | At Baseline and Up to 12.5 Weeks | |
Primary | Effects of FEED-FF diet on quality of life | Measured by using the European Organization for the Research and Treatment of Cancer (EORTC) Quality of Life (QoL) Survey; FEED-FF arm hypothesized to demonstrate more favorable QoL compared to SUC arm. | At Baseline, Week 6.5 and Up to 12.5 Weeks | |
Primary | Efficacy of the FEED-FF intervention | Measured by an accrual rate of 50% of eligible patients, fermented foods (FF) intake of at least 3 servings on at least 80% of days, and at least 80% of intervention group reporting high/very high satisfaction with intervention.
Weekly goal adherence via randomly administered food logs, tracking responses to and general completion of an exit survey will be utilized. |
At Baseline, Week 6.5 and Up to 12.5 Weeks | |
Primary | Feasibility of the FEED-FF intervention | Measured by an accrual rate of 50% of eligible patients, fermented foods (FF) intake of at least 3 servings on at least 80% of days, and at least 80% of intervention group reporting high/very high satisfaction with intervention.
Weekly goal adherence via randomly administered food logs, tracking responses to and general completion of an exit survey will be utilized. |
At Baseline, Week 6.5 and Up to 12.5 Weeks |
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