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Living Well With Lymphoma: Fatigue Reduction Diet

This study, called "Living Well With Lymphoma," is looking for people aged 18 and older who have been diagnosed with lymphoma (Hodgkin or non-Hodgkin) and experience ongoing fatigue related to their lymphoma. You would be randomly assigned to one of two groups. One group will receive eight sessions of counseling on a Fatigue Reduction Diet, which involves replacing some daily calories with specific foods like whole grains. The other group will receive eight sessions of counseling on general health topics, excluding diet. The main goal is to see if the Fatigue Reduction Diet helps reduce fatigue after 3 months. The study plans to enroll 100 participants, but its current recruitment status is unclear.

Study design
This interventional study plans to enroll 100 participants with lymphoma and persistent fatigue. Participants will be randomly assigned to one of two counseling groups.
What's involved
Participants will attend 8 counseling sessions, each lasting about 15 minutes, delivered by phone or video conferencing. The study duration for interventions is 3 months.
Compensation
Not stated in the trial record.
Follow-up
Fatigue will be measured at 3 months after enrollment.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06047626

Living Well With Lymphoma

Recruiting
NAAges 18+InterventionalSupportive care
University of Michigan Rogel Cancer Center
~100 participants
Updated 2025-10-30 on ClinicalTrials.gov
What's tested:Fatigue Reduction DietGeneral Health Curriculum

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Brief Fatigue Inventory
Measured over 3 months after enrollment

Conditions

Lymphoma

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NCT06047626

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • University of Michigan

    Ann Arbor, Michiganstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

Study leadership

  • Suzie Zick · PRINCIPAL_INVESTIGATOR · University of Michigan Rogel Cancer Center

Who to contact

Sara Snyder
[email protected]
734-998-7124
Email the study team

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Eligibility criteria

Inclusion

Women and men aged 18 years and older
Diagnosis of lymphoma (Hodgkin and non-Hodgkin)
Have an average persistent fatigue defined as ≥ 4 on the Brief Fatigue Inventory
Fatigue must be attributed to lymphoma diagnosis
Fatigue onset must be between 12months before diagnosis and any time after diagnosis
Fatigue must not be attributed to other disease diagnoses
Fruit and vegetable intake ≤5.5 servings/day
Have, or be willing to create, an email address to receive study questionnaires electronically.

Exclusion

Medically unstable
BMI\<18.5 kg/m2
Have a current untreated diagnosis of mood disorder, e.g., bipolar or major depressive disorder
Have a current untreated diagnosis of anemia
Have a current untreated diagnosis of hypothyroidism
Have an initiation, a cessation or change of treatment of any chronic medications, dietary supplements, behavioral therapy, physical therapy etc., or any planned change of medications, supplements, or therapies during the study
Have a current diagnoses of cachexia
Planning on becoming pregnant, currently pregnant or lactating

What this trial measures

  • Brief Fatigue Inventory3 months after enrollment

    To examine the effect of 3 months of FRD compared to an attention control GHC on persistent fatigue, measured with the Brief Fatigue Inventory. The instrument consists of 9 items, each measuring fatigue on a 0-10 scale, and is calculated from the mean of completed items