Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05839210

Lifestyle Intervention of Food and Exercise for Lymphoma Survivors

Led by University of Miami · Updated on 2026-01-30

140

Participants Needed

1

Research Sites

183 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to investigate if a mediterranean diet and exercise program for Lymphoma patients during chemotherapy can improve treatment completion and reduce treatment-related side effects.

CONDITIONS

Official Title

Lifestyle Intervention of Food and Exercise for Lymphoma Survivors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or older
  • Any sex/gender
  • Able to provide consent
  • Able to read or understand English or Spanish
  • Diagnosis of untreated Non-Hodgkin or Hodgkin lymphoma requiring at least 6 cycles of chemotherapy
  • Receiving chemotherapy with R-CHOP or R-CHOP-like regimen, BR, BV-AVD, ABVD, or checkpoint inhibitor plus AVD
  • ECOG Performance Status grade less than 2 (PI approval if ECOG = 2)
  • Approval from treating oncologist
  • Receiving chemotherapy at Sylvester Comprehensive Cancer Center or University of Miami Hospital/UHealth Tower
  • Access to internet on a smartphone, tablet, or computer
  • Willing to be randomized to Mediterranean diet/home-based physical activity intervention or waitlist-control group
Not Eligible

You will not qualify if you...

  • Younger than 18 years of age
  • Unable to provide consent
  • Unable to read or understand English or Spanish
  • Any contraindication for diet change or exercising as determined by physician
  • Currently following a vegan or ketogenic diet or consuming more than 5 servings of fruits and vegetables per day in the prior month
  • Engaging in more than 150 minutes of moderate to vigorous physical activity per week in the prior month
  • History of dementia or major psychiatric disease
  • History of stroke, myocardial infarction, or congestive heart failure within the past year

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Miami

Miami, Florida, United States, 33136

Actively Recruiting

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Research Team

T

Tracy E Crane, PhD, RDN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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