Questionnaire Study for Gynecological Cancer Survivors

Status unconfirmed

Conditions studied: Endometrial Neoplasms, Ovarian Neoplasms, Uterine Cervical Neoplasms, Vulvar Neoplasms, Vaginal Neoplasms, Genital Neoplasms, Female

In brief

The purpose of this study is to evaluate the quality of life of long-term gynecologic cancer survivors.

Key facts

Study ID

NCT00391664

Run by

U.S. Army Medical Research and Development Command

People needed

1000

Starts

2006-02-01

Expected to finish

2011-02-01

Last updated by the study team

2008-06-30

Who can join

Age: 20 and older, up to 75. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Female participants diagnosed with gynecologic cancer
• Participants between the ages of 20 and 75 years old, inclusive
• Participants previously treated for all stages (I-IV) of the following cancers: cervix; endometrium; ovary; vulva; vagina; and other genital cancers
• Participants receiving treatment for their primary cancer in the past 2-10 years

You may not qualify if…

• Male participants
• Participants with major psychoses (e.g. organic brain syndrome; schizophrenia; bipolar disorder; or mental retardation).
• Participants with significant hearing deficit
• Participants with prior non-gynecologic cancer diagnosis
• Participants who refused all forms of cancer treatment, whether standard of care or experimental.
• Participants with deficient ability to read/speak English
• Participants residing >90 miles from the research site
• Participants diagnosed with dementia
• Participants diagnosed with pregnancy

Where it is running

• Walter Reed Army Medical Center — Washington D.C., District of Columbia, United States (enrolling)
• Ohio State University — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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