Quality of Life Associated With a Low-Risk Screening Program for Ovarian Cancer

• Conditions: Ovarian Cancer
• Interventions: Behavioral: Questionnaire

• Registration Number: NCT00511641
• Lead Sponsor: M.D. Anderson Cancer Center

Brief Summary

The goal of this research study is to learn more about how women feel about an ovarian cancer screening program that involves getting a blood test to measure CA 125 levels. This includes finding out about women's quality of life and whether they are concerned or worried about their risk of developing cancer. This study also seeks to find out whether elevated CA 125 levels affect participants in terms of cancer worries or concerns.

Detailed Description

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 MD Anderson.

Study Timeline

• Study Start: 2002-02-12
• Study First Submitted: 2007-08-03
• Study First Submitted QC: 2007-08-03
• Study First Posted: 2007-08-06
• Status Verified: 2019-06
• Last Update Submitted: 2019-06-20
• Last Update Posted: 2019-06-24
• Primary Completion: 2020-02
• Study Completion: 2021-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 1342

Inclusion Criteria

1. Women enrolled on protocol ID01-022

   • Women > 50 years of age
   • Postmenopausal (> 12 months amenorrhea)
   • Willingness to return to clinic for annual blood tests, or earlier if indicated
   • Willingness to undergo transvaginal ultrasound if indicated

2. Women who speak and read English

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Exclusion Criteria

1. Women ineligible to be enrolled on protocol ID01-022

   • Prior removal of both ovaries

   • Active non-ovarian malignancy

   • Women who have a history of non-ovarian malignancy will be eligible if they have no persistent or recurrent disease and have not received treatment for > 12 months. They will not be excluded if they are on tamoxifen.

   • High-risk for ovarian cancer due to familial predisposition as defined by the following:

     • Known mutation in BRCA1 or BRCA2
     • Two first or second degree relatives with either ovarian cancer or pre-menopausal breast cancer
     • Ashkenazi Jewish ethnicity with one first degree or two second degree relatives with pre-menopausal breast or ovarian cancer, or if patient herself has had breast cancer.

2. Women who do not speak or read English

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Low Risk OVCA	Questionnaire	Patient that is participating in an ovarian cancer (OVCA) screening program.

Primary Outcome Measures

Name	Time	Method
Mean Scores on Each Quality of Life Instrument (Surveys)	Baseline quality of life data collected, and if/when return to clinic due to abnormal test results.	Descriptive, written, self-report, quality of life instruments used.

Secondary Outcome Measures

Name	Time	Method
To find out whether elevated CA 125 levels affect participants in terms of cancer worries or concerns.	8 Years

Trial Locations

Locations (1)

University of Texas MD Anderson Cancer Center; 🇺🇸 Houston, Texas, United States