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Cancer Survivors Acute Exercise Response 1

Not Applicable
Conditions
Neoplasms Malignant
Interventions
Other: Exercise
Registration Number
NCT03903848
Lead Sponsor
University of Houston
Brief Summary

The aims of this study examine the immune system, muscle metabolism, and autonomic nervous system response to an acute bout of exercise. Cancer survivors will participate in an acute bout of exercise. Blood samples will be collected before the exercise bout and at two time points after the exercise bout to assess the proposed variables.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
18
Inclusion Criteria
  • Between the ages of 40-70 years

    • At least two years past detectible cancer (two years disease-free survival)
    • Have received chemotherapy and/or radiation as part of their cancer treatment
    • All cancers were of the organs/non-blood producing tissues (not blood/hematologic cancers) and while they were an adult (no history of pediatric cancer)
    • Meeting ACSM-AHA guidelines for exercise (150 minutes per week of cardiorespiratory fitness type exercises and ~two days per week of resistance training), as confirmed by a combination of a physical activity questionnaire and a cardiorespiratory fitness classification of "good" or higher (age and sex matched)
    • A BMI between 20-33 kg·m-2
    • Able to speak and read English
Exclusion Criteria

Participants may not:

  • Have any contraindications to moderate to vigorous exercise
  • Have any recent illness or have been instructed not to exercise by a healthcare provider
  • Participants may not have range of motion restrictions that would prevent them from participating in aerobic or resistance training with proper form (they must be ambulatory)
  • Be taking medications (prescription or over the counter) known to influence immune function (including daily NSAID's and beta blockers), cholesterol-lowering medications (statins), drugs that increase bone mass (bisphosphonates), or steroids.
  • Have known cardiovascular, respiratory, metabolic, or renal disease, with the exception of controlled hypertension (as defined by resting BP below 140/90) and/or controlled asthma (self-reported).
  • Be pregnant
  • Be unable to complete all visits (i.e. must not be planning to leave the Houston area long-term before concluding their participation in the study)
  • Fall outside of a BMI range of (20 - 33)
  • Consume alcohol or recreational drugs for 24h prior to visits
  • Participants must not have scheduling conflicts that would prevent them from reporting to the laboratory of integrated physiology 2-3 times over the course of the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Exercise sessionExerciseOne session of physical exercise
Primary Outcome Measures
NameTimeMethod
Exercise-induced response of circulating GDF-15Pre-exercise, change from pre-exercise to immediately post-exercise, change from pre-exercise to 1hr post-exercise, change from immediately post-exercise to 1hr post-exercise

Circulating serum growth differentiation factor 15 before and after one exercise session

Exercise-induced response of circulating monocytesPre-exercise, change from pre-exercise to immediately post-exercise, change from pre-exercise to 1hr post-exercise, change from immediately post-exercise to 1hr post-exercise

Circulating serum monocyte phenotype before and after one exercise session

Exercise-induced response of circulating T cellsPre-exercise, change from pre-exercise to immediately post-exercise, change from pre-exercise to 1hr post-exercise, change from immediately post-exercise to 1hr post-exercise

Circulating serum T cells phenotype before and after one exercise session

Exercise-induced response of circulating FollistatinPre-exercise, change from pre-exercise to immediately post-exercise, change from pre-exercise to 1hr post-exercise, change from immediately post-exercise to 1hr post-exercise

Circulating serum follistatin before and after one exercise session

Secondary Outcome Measures
NameTimeMethod
Body compositionbefore exercise

Relative body composition, as calculated from a DEXA scan. Measurement will be used as a descriptive variable and potential covariant

Body weightbefore exercise

Absolute body weight as measured with an eye level beam. Measurement will be used as a descriptive variable and potential covariant

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