Home
Search
Study Topics
Glossary
|
|
|
|
|
|
Sponsored by: |
M.D. Anderson Cancer Center |
---|---|
Information provided by: | M.D. Anderson Cancer Center |
ClinicalTrials.gov Identifier: | NCT00511641 |
Primary Objectives:
Condition | Intervention |
---|---|
Ovarian Cancer |
Behavioral: Questionnaire |
Study Type: | Observational |
Study Design: | Case-Only, Prospective |
Official Title: | Quality of Life Associated With a Low-Risk Screening Program for Ovarian Cancer |
Estimated Enrollment: | 2400 |
Study Start Date: | February 2002 |
Estimated Primary Completion Date: | February 2010 (Final data collection date for primary outcome measure) |
Groups/Cohorts | Assigned Interventions |
---|---|
1
Patient that is participating in an ovarian cancer screening program.
|
Behavioral: Questionnaire
Questionnaires lasting up to 30 minutes.
|
Participants in this study will be asked to complete several questionnaires. Participants will be able to fill out the questionnaires in the clinic or if necessary, they can complete them at home. Pre-addressed and stamped envelopes will be provided to mail back if they are completed at home. The questionnaires involve quality of life issues, concerns or worries about cancer risk and beliefs about cancer. It will take 30 minutes or less to complete the questionnaires.
The completed questionnaires can be returned to the research nurse or if the participant prefers or they can be returned to the researchers in the self-addressed stamped envelope that is provided.
This is an investigational study. This study will involve 2400 women who are participating in an ovarian cancer screening program. All will be enrolled at M.D. Anderson.
Ages Eligible for Study: | 50 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Patient that is participating in an ovarian cancer screening program.
Inclusion Criteria:
Women enrolled on protocol ID01-022
Exclusion Criteria:
Women ineligible to be enrolled on protocol ID01-022
High-risk for ovarian cancer due to familial predisposition as defined by the following:
Contact: Charlotte C. Sun, DrPH | 713-745-4380 |
United States, Texas | |
U.T.M.D. Anderson Cancer Center | Recruiting |
Houston, Texas, United States, 77030 | |
Principal Investigator: Diane C. Bodurka, MD |
Principal Investigator: | Diane C. Bodurka, MD | U.T.M.D. Anderson Cancer Center |
Responsible Party: | U.T.M.D. Anderson Cancer Center ( Diane C. Bodurka, MD/Associate Professor ) |
Study ID Numbers: | ID01-693 |
Study First Received: | August 3, 2007 |
Last Updated: | October 22, 2008 |
ClinicalTrials.gov Identifier: | NCT00511641 |
Health Authority: | United States: Institutional Review Board |
Ovarian Cancer Cancer Screening Quality of Life |
Questionnaire Screening Survey |
Genital Diseases, Female Ovarian cancer Ovarian Neoplasms Gonadal Disorders Genital Neoplasms, Female Quality of Life |
Endocrine System Diseases Urogenital Neoplasms Endocrinopathy Ovarian Diseases Endocrine Gland Neoplasms |
Neoplasms Neoplasms by Site Adnexal Diseases |