Primary Objectives
• To assess the tolerability and feasibility of Intermittent fasting (IF) in participants at high risk for pancreatic cancer.
Secondary Objectives
* To assess changes in oral and gut microbiome after IF.
* To assess changes in metabolomic markers after IF.
* To assess changes in inflammatory markers after IF.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Participants ≥ 18 years old. Participants under 18 are excluded due to their potential inability to understand and consent independently to the methods required for the study drug use and its potential risks and benefits.
Participants evaluated and classified as high risk for pancreatic cancer through a High-Risk Pancreatic Cancer Clinic or High-Risk Pancreatic Cyst Clinic, based on established clinical assessment and risk stratification.
High-risk status may include one or more of the following:
* Hereditary cancer syndromes or known pathogenic germline mutations associated with pancreatic cancer risk
* Family history of pancreatic ductal adenocarcinoma (PDAC)
* Presence of pancreatic cysts or precursor lesions (e.g., IPMN, MCN)
* New-onset diabetes mellitus is considered suspicious for pancreatic cancer
* History of recurrent or chronic pancreatitis
Eligibility and surveillance risk assessment must be consistent with NCCN (National Comprehensive Cancer Network) Guidelines for Pancreatic Cancer Screening in High- Risk Individuals.
Participants are able to understand and are willing to sign a written informed consent document.
Both English-speaking and non-English-speaking participants are eligible for participation
Participants are willing to make a change in eating time patterns.
Participants are willing to provide App-tracked fasting time data over the course of the study.
