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Search / Trial NCT06862323

Time Restricted Eating in Haematological Malignancies

Launched by BRITISH COLUMBIA CANCER AGENCY · Mar 3, 2025

Trial Information

Current as of August 22, 2025

Not yet recruiting

Keywords

Time Restricted Eating Intermittent Fasting Diet Cancer Chronic Lymphocytic Leukemia Autophagy Microbiome Inflammation Epigenetics

ClinConnect Summary

This clinical trial, titled "Time Restricted Eating in Haematological Malignancies," is exploring whether a specific eating pattern called time-restricted eating (TRE) can help improve health for patients with chronic lymphocytic leukemia (CLL), a type of cancer. TRE involves eating normally for 8 hours each day and fasting for the remaining 16 hours. The trial aims to see if this eating pattern can lower cancer cell counts, affect immune cell recycling (a process that keeps cells healthy), and enhance the overall quality of life for participants.

To be eligible for this study, participants must be between 18 to 85 years old and have a diagnosis of CLL or a similar condition. They should not have followed any form of intermittent fasting for the four months before joining the study. Participants will be asked to follow the TRE regimen for either 3 or 6 months, keep track of their meals and weight, and attend regular check-ins with the study team. They will also provide blood samples and complete questionnaires about their quality of life. This study is currently not recruiting participants, but it is important for those interested to know that they will need to meet specific health criteria to join.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Experimental Participants:
  • Diagnosis of CLL or SLL, Age 18-85
  • Peripheral blood lymphocytes \>20 x 10\^9/L
  • Hemoglobin \>90g/L
  • Platelets ˃90 x 10\^9/L
  • BMI of \>=20kg/m2
  • ECOG Performance Status \>=2
  • Not following any form of IF for 4 months prior to study
  • Control Participants:
  • Absence of cancer diagnosis (active or historical)
  • Age 18-85, Peripheral blood lymphocytes \<5 x10\^9/L
  • BMI of \>=20kg/m2
  • ECOG Performance Status \>=2
  • Not following any form of IF for 4 months prior to study
  • Exclusion Criteria:
  • Experimental and Control Participants:
  • Unable to give consent
  • On medications required to be taken with food during the fasting window
  • Pregnant or breastfeeding
  • Diabetes mellitus
  • BMI drop to \< 18.5kg/m2 at any time during study
  • Anti-lymphoma therapy within the past 3 months
  • Expected to initiate anti-lymphoma therapy within the next 3 months
  • Unable to fast due to a digestive system disorder
  • \> 85 years of age (due to frailty, increased risk of infection, and burden of additional blood collections)

About British Columbia Cancer Agency

The British Columbia Cancer Agency (BCCA) is a leading organization dedicated to cancer research, treatment, and prevention in Canada. As a prominent clinical trial sponsor, BCCA focuses on advancing cancer care through innovative research and the development of new therapeutic strategies. With a commitment to improving patient outcomes, BCCA collaborates with a network of healthcare professionals and research institutions to conduct rigorous clinical trials that explore cutting-edge treatments and diagnostic methods. Their multidisciplinary approach, combined with a strong emphasis on patient-centered care, positions BCCA at the forefront of cancer research and healthcare advancements.

Locations

Victoria, British Columbia, Canada

Patients applied

0 patients applied

Trial Officials

Eleah Stringer, MSc, RD, CSO

Principal Investigator

BC Cancer

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported