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Influence of Adiposity on IGF-1 and Fitness Response to Exercise in Cancer Survivors

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status

Completed

Conditions

Overweight and Obesity
Cancer

Treatments

Behavioral: Aerobic Exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT05558384
22-0356.ccc

Details and patient eligibility

About

This is a pilot feasibility study of an investigation of the influence of excess adiposity on cardiorespiratory fitness (CRF), insulin-like growth factor-1 (IGF-1), and metabolic responses to a standardized aerobic exercise program in cancer survivors. This investigation attempts to isolate the influence of adiposity on these responses. We will enroll overweight, obese, and normal weight cancer survivors with a primary diagnosis of breast, prostate, or colorectal cancer who have completed all cancer-related treatment. Participants will engage in a 15-week aerobic exercise intervention with pre- and post-intervention assessments.

Enrollment

12 patients

Sex

All

Ages

21 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Primary cancer diagnosis of breast, prostate, or colorectal cancer

  • Completion of all cancer-related treatment > than 6 months prior and < 5 years prior to enrollment

  • Ability and willingness to participate in a supervised exercise program

    • All participants will be required to obtain a signed physician clearance to participate in exercise form prior to enrollment

Exclusion criteria

  • Presence of a secondary active cancer diagnosis or metastatic disease

  • Any current cancer treatment (including hormonal treatment) or planned cancer treatment in the next 5 months

  • Greater than 100 min of self-reported regular exercise per week

  • BMI < 18.5 (underweight)

  • Any significant metabolic condition, such as diabetes. Individuals with pre-diabetes or metabolic syndrome will not be excluded, but this information will be recorded.

  • Any medical condition that would impact the safety of, or participation in, an exercise program or exercise testing, including:

    • Orthopedic conditions such as advanced osteoarthritis, mobility-limiting amputations or chronic injuries, or mobility-limiting acute orthopedic injuries
    • Advanced rheumatoid arthritis or chronic widespread pain conditions such as fibromyalgia
    • Pulmonary conditions such as chronic obstructive pulmonary disease, emphysema, or interstitial lung disease
    • Known cardiovascular disease, uncontrolled hypertension, or new cardiac event within the past 6 months

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

Aerobic exercise
Experimental group
Description:
15-week standardized aerobic exercise intervention
Treatment:
Behavioral: Aerobic Exercise

Trial contacts and locations

1

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Central trial contact

Ryan Marker; Jared Scorsone

Data sourced from clinicaltrials.gov

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