Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT04832763

Medical and Psychosocial Issues in Adolescents and Young Adults With Colorectal Cancer

Colorectal Cancer in Adolescents and Young Adults: A Pilot Study of Medical and Psychosocial Issues

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
32 (actual)
Sponsor
University of Southern California · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study investigates the medical and psychosocial consequences of colorectal cancer on adolescents and young adults. Measuring physical function in adolescents and young adults with colorectal cancer may help doctors better understand the level of physical function during cancer treatment and how to improve the management of colorectal cancer in adolescents and young adults. This study may also help design a future exercise program to decrease risk factors including high blood pressure, high blood sugar, and high cholesterol.

Detailed description

PRIMARY OBJECTIVES: I. To prospectively characterize the symptom burden and assess the health-related quality of life of adolescents and young adults (AYAs) in active treatment for colorectal cancer in comparison to older patients to identify differences that contribute to the development of appropriately timed, age appropriate interventions. II. To characterize the symptom burden and assess the health-related quality of life of AYAs who have completed curative therapy and are in surveillance for colorectal cancer compared to older patients to identify differences that contribute to the development of appropriately timed, age-appropriate interventions. SECONDARY OBJECTIVE: I. Using a prospective and cross-sectional design, characterize physical function, body composition, and biomarkers of comorbid conditions among AYAs with colorectal cancer (CRC) on active therapy and after completion of therapy in survivorship to identify targets for and timing of interventions. EXPLORATORY OBJECTIVE: I. To assess across Aims differences by cancer site (colon versus \[vs.\] rectal) by sex, and by race/ethnicity. OUTLINE: Patients on active treatment complete questionnaires and undergo collection of blood samples and physical function assessments at baseline, and at 3 and 6 months. Survivors in surveillance complete questionnaires and undergo collection of blood sample and physical function assessment at baseline.

Conditions

Interventions

TypeNameDescription
PROCEDUREBiospecimen CollectionUndergo collection of blood sample
OTHERMedical Chart ReviewReview of medical charts
OTHERPhysical Performance TestingUndergo physical function testing
OTHERQuality-of-Life AssessmentAncillary studies
OTHERQuestionnaire AdministrationComplete questionnaire

Timeline

Start date
2019-09-27
Primary completion
2026-12-31
Completion
2027-12-31
First posted
2021-04-06
Last updated
2025-12-22

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT04832763. Inclusion in this directory is not an endorsement.