Lifestyle Intervention for Lymphoma Survivors

This study is looking at whether a special diet and exercise program can help people with Non-Hodgkin Lymphoma or Hodgkin Lymphoma during chemotherapy. You would follow a Mediterranean Diet (LIFE-L Mediterranean Diet) and a Home-Based Exercise Program (LIFE-L Home-Based Exercise Program). You'll also receive supportive materials like an informational notebook, exercise poster and videos, a Fitbit, and stretch bands, along with text messages or emails. The researchers want to see if these interventions help you complete your treatment and reduce side effects. To join, you need to be 18 or older, able to give consent, and understand English or Spanish. You also need a diagnosis of untreated Non-Hodgkin or Hodgkin lymphoma requiring at least 6 cycles of chemotherapy with specific regimens like R-CHOP or BR. The study is currently unclear on its recruitment status and plans to enroll 140 participants.

Study design
This is an interventional study, meaning participants will receive specific interventions. It aims to enroll 140 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your satisfaction will be measured up to 30 weeks after the intervention.

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NCT05839210

Lifestyle Intervention of Food and Exercise for Lymphoma Survivors

Recruiting
NAAges 18+Interventional
University of Miami
~140 participants
Updated 2026-01-30 on ClinicalTrials.gov
What's tested:LIFE-L Mediterranean DietLIFE-L Home-Based Exercise ProgramSupportive Materials

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percentage of Survivors who participate
Measured over Up to 12 months
+2 more outcomes measured
Non Hodgkin Lymphoma
Hodgkin Lymphoma
1 sites across 1 states
Florida1
  • Tracy E Crane, Phd, RDN · PRINCIPAL_INVESTIGATOR · University of Miami
  • Craig Moskowitz, MD · PRINCIPAL_INVESTIGATOR · University of Miami

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  • Percentage of Survivors who participateUp to 12 months

    Percentage of survivors who agree to participate out of the total number of participants recruited will be assessed using a threshold of greater than or equal to (\>=) 50-percent.

  • Percentage of Participants Completing Intervention SessionsUp to 26 weeks (Post-Intervention)

    Percentage of intervention session completion at the end of treatment will be assessed, using a threshold of greater than or equal to (\>=) 80-percent.

  • Change in percentage of participant satisfaction4 weeks (post-intervention), up to 30 weeks

    The change in percentage of participant satisfaction rate at the end of study participation will be assessed, using a threshold of greater than or equal to (\>=) 80-percent. Participant satisfaction will be assessed via exit interviews.