MedTrace Logo

Questionnaire Study for Gynecological Cancer Survivors

NCT00391664 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2008-06-30

No results posted yet for this study

Summary

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

Conditions

  • Endometrial Neoplasms
  • Ovarian Neoplasms
  • Uterine Cervical Neoplasms
  • Vulvar Neoplasms
  • Vaginal Neoplasms
  • Genital Neoplasms, Female

Interventions

BEHAVIORAL

Psychosocial

Sponsors & Collaborators

  • Walter Reed Army Medical Center

    collaborator FED

  • Ohio State University

    collaborator OTHER

  • U.S. Army Medical Research and Development Command

    lead FED

Principal Investigators

  • Barbara L Andersen, PhD · Ohio State University

  • LTC G. Larry Maxwell, MD · Walter Reed Army Medical Center

Eligibility

Min Age
20 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-02-28
Completion
2011-02-28

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00391664 on ClinicalTrials.gov