Actively Recruiting

Age: 18Years - 39Years
All Genders
NCT04551378

The Effect of COVID-19 Pandemic on Adolescent and Young Adult Cancer Patients and Survivors

Led by M.D. Anderson Cancer Center · Updated on 2025-10-21

600

Participants Needed

1

Research Sites

285 weeks

Total Duration

On this page

Sponsors

M

M.D. Anderson Cancer Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study investigates how the COVID-19 pandemic has impacted the psychological, financial, physical, and social well-being of adolescent and young adult (AYA) cancer patients and survivors. AYA cancer survivors have inferior long-term survival compared to the general population, and the negative impact of the global COVID-19 pandemic may be even higher in this vulnerable group. The information gained from this study may provide an opportunity to determine the self-reported COVID-19 specific psychological distress in AYA cancer survivors, and may lead to the development of a targeted intervention to improve physical and psychosocial health for AYA cancer patients and survivors.

CONDITIONS

Official Title

The Effect of COVID-19 Pandemic on Adolescent and Young Adult Cancer Patients and Survivors

Who Can Participate

Age: 18Years - 39Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Initial cancer diagnosis between the ages of 15 to 39
  • Received any cancer treatment at MD Anderson Cancer Center with data available in the Tumor Registry
  • Confirmed alive at time of contact for questionnaire completion
Not Eligible

You will not qualify if you...

  • Inability to complete questionnaires in English
  • Seen at MD Anderson for a second opinion or non-treatment related visit

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

M

Michael E Roth, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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