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Predictors of physical activity maintenance in colorectal cancer survivors

Study category: Cancer

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Description

Supervised low to moderate intensity aerobic and resistance exercise, twice per week for 60 minutes. Four, 1-hour PA behavior change education/discussion sessions.

Details
Age

Adult

Eligibility

- Be a male or female aged 50-80 - Histologically confirmed cancer of the colon or rectum (stages II-III) - Completed resection or other surgery 3-24 months prior to enrollment - Received and completed any chemotherapy and/or radiation within one the previous year - No evidence of metastatic disease - No known contraindications for exercise or not able to safely participate in exercise

Detailed Eligibility: Inclusion Criteria: 1. Provision to sign and date the consent form 2. Fluent in English 3. Stated willingness to comply with all study procedures and be available for the duration of the study 4. Be a male or female aged 50-80 5. Histologically confirmed cancer of the colon or rectum (stages II-III) 6. Completed resection or other surgery 3-24 months prior to enrollment 7. Received and completed any chemotherapy and/or radiation within one the previous year Exclusion Criteria: 1. Evidence of metastatic disease 2. Existing participation in greater than or equal to 150 minutes per week of at least moderate intensity PA 3. Known contraindications for exercise or not able to safely participate in exercise 4. Pregnant women (no testing required)

Phase

III - Research Studies that gather more information about a drug's safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs. These studies typically involve more participants.

Type of Study

Supportive Care

Locations

Anschutz Health and Wellness
Colorado State University
Harmony Campus
Poudre Valley Hospital
UCD Anschutz Health & Wellness Center

Principal Investigator
Wells Messersmith,  MD

Wells Messersmith, MD

Study ID

Protocol Number: 18-2436

More information available at ClinicalTrials.gov: NCT03781154

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