Clinical trial · Interventional
Time-restricted Eating and Healthy Eating in Patients With Metabolic Liver Disease or Cancer
Feasibility Study of Time Restricted Eating and a Healthy Diet in Patients Receiving Liver-Directed Therapy for Hepatocellular Carcinoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a feasibility study that will collect data to assess the potential effect of nutritional intervention. This prospective single-site trial will enroll adult patients with liver diseases such as metabolic-dysfunction associated steatotic liver disease (MASLD), metabolic-dysfunction associated steatohepatitis (MASH), cirrhosis and/or hepatocellular carcinoma (HCC). Eligible individuals who are randomized to the intervention group will be enrolled in a six-month nutritional change program consisting of time-restricted eating plus targeted healthy changes in what they eat (TR-HE). The intervention includes dietary counseling visits with a study registered dietitian (RD) and motivational phone calls with a study Certified Health and Wellness Coach (HC). Individuals who are randomized to the control group or who elect to join the control group will be enrolled in a six-month period of observation and phlebotomy only. The main questions it aims to answer are: Is a prolonged nightly fast coupled with a healthy diet safe and feasible for patients with liver disease or cancer? Does the intervention improve liver metabolism?
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Liver Cancer, Adult | Malignant Liver Neoplasm | CURATED_EXACT | 0.85 |
| MASH - Metabolic Dysfunction-Associated Steatohepatitis | — | UNRESOLVED | — |
| Obesity and Overweight | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Time-restricted eating plus healthy diet | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Intervention
- description
- Intervention group will follow time-restricted consumption of a healthy diet.
- interventionNames
- Behavioral: Time-restricted eating plus healthy diet
- type
- NO_INTERVENTION
- label
- Control
- description
- Control observational arm.
Primary outcomes (4)
- measure
- Adherence to protocol
- timeFrame
- 6 months
- description
- Participant adherence to and comprehension of the protocol as an indicator of intervention delivery by staff. Adherence will be assessed by the number of participants who complete the study, the percentage of days with fasting \>14 h, and the number of days that food was logged into the app.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Overweight or obese (BMI 27-45 kg/m2) 2. Diagnosed with metabolic-dysfunction associated steatitic liver disease (MASLD/NAFLD), metabolic-dysfunction associated steatohepatitis, cirrhosis or liver cancer (BCLC early to intermediate stage HCC) 3. English or Spanish speaking over the age of 18. 4. ECOG Performance Status ≤ 2. 5. Usual nightly fasting \<12 hours 6. Willing to comply with all study procedures 7. Life expectancy of \> 12 months Exclusion Criteria: 1. Advanced HCC, progression, and/or associated comorbidities 2. Metastatic disease, tumor in vein, or ascites 3. Advanced Cirrhosis (hypoalbuminemia/Child-Pugh B+C). 4. Poorly controlled or refractory (grade 3-4) hepatic encephalopathy 5. Type 1 diabetes or self-reported hypoglycemia or hypoglycemic events by CGM 6. Participation in another conflicting study that requires modification of diet or food timing. 7. Patients on GLP-1 receptor agonists 8. Uncontrollable eating pattern (e.g., wasting, Night Eating Syndrome, disordered eating habits, food insecurity) 9. Medications that markedly impact metabolic study biomarkers. 10. Other cancer in last 10 years (other than nonmelanoma skin cancer or carcinoma of the cervix in situ) 11. Serious medical conditions such as chronic kidney disease, congestive heart failure, or any condition that would interfere with participation in the trial. 12. Unresolved toxicity ≥ CTCAE Grade 2 from previous anti-cancer therapy 13. Active alcohol abuse or less than 6 months of sobriety 14. Participation in a trial of an investigational agent within the prior 30 days 15. Pregnancy or lactating, positive hCG urine test.
References
Publications (2)
- BACKGROUNDDas M, Kumar D, Sauceda C, Oberg A, Ellies LG, Zeng L, Jih LJ, Newton IG, Webster NJG. Time-Restricted Feeding Attenuates Metabolic Dysfunction-Associated Steatohepatitis and Hepatocellular Carcinoma in Obese Male Mice. Cancers (Basel). 2024 Apr 16;16(8):1513. doi: 10.3390/cancers16081513. PMID 38672595
- BACKGROUNDDas M, Webster NJG. Obesity, cancer risk, and time-restricted eating. Cancer Metastasis Rev. 2022 Sep;41(3):697-717. doi: 10.1007/s10555-022-10061-3. Epub 2022 Aug 19. PMID 35984550