Status:
UNKNOWN
Questionnaire Study for Gynecological Cancer Survivors
Lead Sponsor:
U.S. Army Medical Research and Development Command
Collaborating Sponsors:
Walter Reed Army Medical Center
Ohio State University
Conditions:
Endometrial Neoplasms
Ovarian Neoplasms
Eligibility:
FEMALE
20-75 years
Brief Summary
The purpose of this study is to evaluate the quality of life of long-term gynecologic cancer survivors.
Detailed Description
Since the early 1970s, death rates for the major gynecological tumors have significantly declined, with a reduction of 42% for endometrial, 49% for cervix, 27% for vagina and vulva, and 11% for ovaria...
Eligibility Criteria
Inclusion
- 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
Exclusion
- 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
Key Trial Info
Start Date :
February 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
February 1 2011
Estimated Enrollment :
1000 Patients enrolled
Trial Details
Trial ID
NCT00391664
Start Date
February 1 2006
End Date
February 1 2011
Last Update
June 30 2008
Active Locations (2)
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1
Walter Reed Army Medical Center
Washington D.C., District of Columbia, United States, 20307
2
Ohio State University
Columbus, Ohio, United States, 43210