The Purpose of This Study is to Determine the Frequency of Colorectal Cancer in Male and Female Endurance Athletes Between the Ages of 35 and 50

NCT ID: NCT05419531

Last Updated: 2025-12-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

94 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-10-18

Study Completion Date

2025-10-22

Brief Summary

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The purpose of this study is to determine the frequency of colorectal cancer in male and female endurance athletes between the ages of 35 and 50.

Detailed Description

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Conditions

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Colorectal Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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prospective observational study - screening and follow up colonoscopy

Involves two visits and a colonoscopy. The first visit will be prior to the colonoscopy. 4-35 days after the colonoscopy, there will be a one time appointment to go over the results of the colonoscopy.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adult males and females 35-50 years of age
* Male and female self-reported endurance athletes, defined by at least one of the following:

* Run at least two races of 50 miles or more
* Run 5 races of 26.2 miles or more
* Ability to complete testing in the protocol and make study visits
* Able and willing to consent to protocol

Exclusion Criteria

* Known or suspected history of inflammatory bowel disease, familial adenomatous polyposis (FAP), or Lynch Syndrome
* Concomitant illness that would prevent adequate patient assessment or in the investigators' opinion pose an added risk for study participants.
* Anticipated poor compliance
* Prisoners or subjects who are involuntarily incarcerated
* Persons with decisional incapacity/cognitive impairment
* Any history or evidence of severe illness or any other condition that would make the patient, in the opinion of the investigator unsuitable for the study
* Subject is involved with a worker's compensation, personal injury, or other legal matters related to their health
* Subject is enrolled in a separate interventional clinical trial
Minimum Eligible Age

35 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Inova Health Care Services

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Timothy Cannon, MD

Role: PRINCIPAL_INVESTIGATOR

Inova Schar Cancer Institute

Locations

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Inova Schar Cancer Institute

Fairfax, Virginia, United States

Site Status

Countries

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United States

References

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Other Identifiers

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U21-10-4567

Identifier Type: -

Identifier Source: org_study_id