Questionnaire for Uterine Cancer Survivors
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to understand pelvic floor issues and quality of life in uterine cancer survivors. Participants will fill out a questionnaire about health, lifestyle, and the impact of cancer treatments. The study seeks individuals who underwent uterine cancer surgery at MD Anderson between 2006 and 2017 and have been disease-free for at least a year. This information could help improve future care and support for survivors. As an unphased trial, this study offers a unique opportunity to contribute to research that could enhance the quality of life for future uterine cancer survivors.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It seems to focus on completing surveys about quality of life and sexual function.
Why are researchers excited about this trial?
Researchers are excited about this trial because it focuses on understanding how pelvic floor dysfunction affects the quality of life in uterine cancer survivors. Unlike traditional treatments that aim to manage the physical symptoms of uterine cancer or its direct side effects, this approach uses detailed questionnaires to gather insights on patients' demographic, treatment history, lifestyle, and comorbidities. Through this method, the trial seeks to illuminate the broader impact of cancer treatment on daily living, offering a chance to identify specific issues that might be overlooked by conventional care. This could lead to more personalized support and interventions to improve survivors' overall well-being.
Who Is on the Research Team?
Lilie L Lin
Principal Investigator
M.D. Anderson Cancer Center
Are You a Good Fit for This Trial?
Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Observational
Participants complete questionnaires over 45-60 minutes assessing quality of life and pelvic floor dysfunction
Follow-up
Participants are monitored for pelvic floor distress and quality of life over time
What Are the Treatments Tested in This Trial?
Interventions
- Questionnaire Administration
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Patients complete questionnaires over 45-60 minutes consisting of demographic, treatment, lifestyle, disease, and comorbidity questions, as well as multiple study instruments assessing quality of life as it pertains to common toxicities of uterine cancer treatment.
Find a Clinic Near You
Who Is Running the Clinical Trial?
M.D. Anderson Cancer Center
Lead Sponsor
National Cancer Institute (NCI)
Collaborator
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