Ovarian Neoplasms Clinical Trial
Official title:
Gynecologic Cancer Survivorship Survey
The purpose of this study is to evaluate the quality of life of long-term gynecologic cancer survivors.
Status | Recruiting |
Enrollment | 1000 |
Est. completion date | February 2011 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 20 Years to 75 Years |
Eligibility |
Inclusion Criteria: - 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 Criteria: - 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 |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | Ohio State University | Columbus | Ohio |
United States | Walter Reed Army Medical Center | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
U.S. Army Medical Research and Materiel Command | Ohio State University, Walter Reed Army Medical Center |
United States,
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