RECRUITING

Feasibility of Non-Operative Management of Rectal Cancer in a Rural Population

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is an observational research study. Patients with rectal cancer can choose different courses of treatment. This study will follow these patients over the course of approximately six years, depending on their treatment. Patients will be monitored through clinic visits and survey assessments to see how they do, how they feel regarding their treatment choices, and their outcomes. The surveys will analyze the impact of the patients' treatment choices, as well as patient adherence, in a rural setting.

Official Title

Feasibility of Non-Operative Management of Rectal Cancer in a Rural Population

Quick Facts

Study Start:2020-02-01
Study Completion:2027-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04245683

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 18 or greater
  2. 2. ECOG PS 0-2
  3. 3. Stage II or III, newly diagnosed, biopsy proven, rectal cancer
  4. 4. No prior treatment for rectal cancer
  5. 5. No prior pelvic radiotherapy
  6. 6. Willing to undergo study related testing and monitoring after treatment
  7. 7. Women of childbearing potential must rule out pregnancy within 2 weeks prior to registration with a blood test or urine study
  8. 8. Women must not be pregnant or breastfeeding
  9. 9. Able to provide informed consent
  1. 1. Patients with metastatic disease
  2. 2. Patients that are not candidates for surgery
  3. 3. Patients that refuse neoadjuvant treatment

Contacts and Locations

Study Contact

Jennifer Victory, RN
CONTACT
6075476965
jennifer.victory@bassett.org
Katelyn Tessier
CONTACT
607-547-3073
kately.tessier@bassett.org

Principal Investigator

Eric Bravin, MD
PRINCIPAL_INVESTIGATOR
Bassett Healthcare

Study Locations (Sites)

Bassett Healthcare Network
Cooperstown, New York, 13326
United States

Collaborators and Investigators

Sponsor: Bassett Healthcare

  • Eric Bravin, MD, PRINCIPAL_INVESTIGATOR, Bassett Healthcare

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-02-01
Study Completion Date2027-08-01

Study Record Updates

Study Start Date2020-02-01
Study Completion Date2027-08-01

Terms related to this study

Additional Relevant MeSH Terms

  • Rectal Cancer