Feasibility of High Intensity Interval Training in Survivors of Childhood, Adolescent, and Young Adult Hodgkin Lymphoma

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10-25
SponsorSt. Jude Children's Research Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participant has been diagnosed with Hodgkin lymphoma between the ages of 10 to 25 years.

Participant is between the ages of >10 and <25 years old the time of enrollment.

Participant has completed treatment (end of chemotherapy for those not receiving radiation therapy or end of radiation therapy) for Hodgkin lymphoma within 24 months prior to enrollment and recovered from any acute treatment-related adverse events.

Participant has been medically cleared to participate in physical activity.

Disqualifiers

Participant has evidence of relapsed disease.

Participant has a diagnosis of acute heart failure.

Participant reports currently participating in HIIT training or >420 minutes per week of moderate to vigorous physical activity.

Female participant who is currently pregnant.

Trial design

Design model

Single group

Treatments tested in this trial

  • High Intensity Interval Training (HIIT)

    Behavioral

    Participants will complete a 12-week HIIT program with three 25-minute sessions per week. Each session includes warm-up, five cycles of high-intensity intervals (80-95% peak HR) and recovery periods (50-60% peak HR), and cool-down.

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: HIIT Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Participation rate (percent of eligible participants approached who enroll)

Descriptive statistics will be reported

Time frame
Trial completion (12 weeks)
2

Completion rate (percentage of scheduled HIIT sessions attended and percentage of post-intervention testing sessions completed)

Descriptive statistics will be reported

Time frame
Trial completion (12 weeks)

Secondary outcomes

Other outcomes

1

Cardiorespiratory fitness (VO2peak, ml/kg/min)

Descriptive statistics of the change between baseline and 12 weeks will be reported

Time frame
baseline at study entry, 12 weeks
2

Ewing battery score of autonomic function (0 to 5 points)

Descriptive statistics of the change between baseline and 12 weeks will be reported

Time frame
baseline at study entry, 12 weeks
3

Body mass index (weight and height will be combined to report body mass index in kg/m2)

Descriptive statistics of the change between baseline and 12 weeks will be reported

Time frame
baseline at study entry, 12 weeks
4

Percent body fat (%)

Descriptive statistics of the change between baseline and 12 weeks will be reported

Time frame
baseline at study entry, 12 weeks

Sponsors and contacts

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