Purpose

The PREFACE Study is a prospective, longitudinal cohort study of reproductive health and clinical outcomes among individuals diagnosed with colorectal cancer between age 18 to 49 years.

Condition

Eligibility

Eligible Ages
Between 18 Years and 49 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Known diagnosis of colorectal cancer - Age 18 to 49 years at colorectal cancer diagnosis - Diagnosed by and/or consulting with a physician participating in the PREFACE Study - No prior history of colorectal cancer and/or colorectal cancer treatment - Mentally and physically able to consent and participate in the study

Exclusion Criteria

  • Women who are pregnant at the time of colorectal cancer diagnosis - Prisoners - Unable to provide informed consent - Unable to read, write, or complete questionnaires in English

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
PREFACE: Vanderbilt-Ingram Cancer Center Patient recruitment and follow-up, longitudinal collection of data and multiple biospecimen at pre-defined study timepoints, objective assessment of health behaviors/habits, individual interviews.

Recruiting Locations

Vanderbilt-Ingram Cancer Center
Nashville, Tennessee 37232
Contact:
PREFACE Study Coordinator (Rebecca B.)
615-936-6204
prefacestudy@vumc.org

More Details

Status
Recruiting
Sponsor
Andreana Holowatyj, PhD, MSCI

Study Contact

PREFACE Study Coordinator (Rebecca B.)
615-936-6204
prefacestudy@vumc.org

Detailed Description

The Preserving Fertility After Colorectal Cancer (PREFACE) Study comprehensively investigates fertility, sexual health and clinical outcomes along the cancer care continuum among individuals diagnosed with colorectal cancer between age 18 to 49 years. Patients are recruited prior to colorectal cancer therapy [baseline] and followed for up to 36 months after completion of first-course therapy (or 45 months after diagnosis for patients on maintenance therapy). Study timepoints are defined at: (i) completion of first-course treatment (or 9 months after diagnosis for patients on maintenance therapy [treatment]); (ii) and at 9, 18 and 36 month intervals thereafter [surveillance]. This cohort is enriched by a robust collection of biospecimens and data.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.