1152 Participants Needed

Survey for Melanoma During COVID-19

LC
Overseen ByLorenzo Cohen
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: M.D. Anderson Cancer Center
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to understand how the COVID-19 pandemic has affected the overall well-being and quality of life in people with melanoma, a type of skin cancer. Researchers seek to learn about the psychological stress related to COVID-19, changes in healthcare, financial impacts, and social interactions. Participants will complete a short, 10-minute survey about these experiences. The trial seeks melanoma patients who have already agreed to share their lifestyle data in a previous study and can be contacted online. As an unphased trial, this study offers participants the opportunity to contribute valuable insights into the broader impacts of the pandemic on the lives of melanoma patients.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It seems to focus on a questionnaire about experiences during the COVID-19 pandemic, so it's unlikely that medication changes are required.

Why are researchers excited about this trial?

Researchers are excited about this trial because it focuses on understanding the well-being and quality of life of melanoma patients during the COVID-19 pandemic through survey administration. Unlike traditional treatments that center on directly attacking melanoma, this approach seeks to gather valuable insights into how patients are coping with the additional stress and challenges posed by the pandemic. By collecting this information, researchers aim to identify specific needs and areas for support, which could lead to improved patient care strategies and mental health interventions tailored to this unique situation.

Who Is on the Research Team?

LC

Lorenzo Cohen

Principal Investigator

M.D. Anderson Cancer Center

Are You a Good Fit for This Trial?

Inclusion Criteria

Patients who have signed consent for PA15-0336
Has an active email address and can be contacted via MyChart
Documentation of being alive per the cancer registr

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Survey Administration

Participants complete a 10-minute survey assessing experiences during the COVID-19 pandemic, psychological distress, and health-related quality of life

Up to 2 months
1 visit (virtual)

Follow-up

Participants are monitored for any changes in psychological distress and health-related quality of life after survey completion

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Survey Administration

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Observational (survey administration)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

M.D. Anderson Cancer Center

Lead Sponsor

Trials
3,107
Recruited
1,813,000+

National Cancer Institute (NCI)

Collaborator

Trials
14,080
Recruited
41,180,000+