Actively Recruiting
Feasibility of High Intensity Interval Training in Survivors of Childhood, Adolescent, and Young Adult Hodgkin Lymphoma
Led by St. Jude Children's Research Hospital · Updated on 2026-04-23
20
Participants Needed
1
Research Sites
143 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This pilot study evaluates the feasibility of a 12-week high intensity interval training (HIIT) program in survivors of childhood, adolescent, and young adult Hodgkin lymphoma within 24 months of completing treatment. Preliminary efficacy of the HIIT intervention for improved cardiorespiratory fitness, body composition, physical function, autonomic response to exercise, peripheral neuropathy, biological aging markers, and physical activity will also be evaluated. Primary Objective: To determine the feasibility of a 12-week high intensity interval training (HIIT) program in survivors of childhood, adolescent, and young adult Hodgkin lymphoma within 24 months of completing treatment. Feasibility will be assessed by: * Participation Rate: Number of eligible survivors approached who enroll. * Completion Rate: Number of scheduled HIIT sessions attended and number of enrolled participants who complete post-intervention testing.
CONDITIONS
Official Title
Feasibility of High Intensity Interval Training in Survivors of Childhood, Adolescent, and Young Adult Hodgkin Lymphoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant diagnosed with Hodgkin lymphoma between 10 and 25 years old
- Participant is older than 10 and younger than 25 years at enrollment
- Completed Hodgkin lymphoma treatment within 24 months prior to enrollment and recovered from acute side effects
- Medically cleared to participate in physical activity
- Understands how to use the web-based platform and study-provided iPad and heart rate monitor
You will not qualify if you...
- Evidence of relapsed Hodgkin lymphoma
- Diagnosis of acute heart failure
- Currently participating in HIIT or more than 420 minutes per week of moderate to vigorous physical activity
- Female participant who is currently pregnant
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
St. Jude Children's Research Hospital
Memphis, Tennessee, United States, 38105
Actively Recruiting
Research Team
A
Amy Berkman, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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