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CompletedNCT00486707Updated Aug 1, 2012

Ovarian Cancer Patient Questionnaire on Genetic Testing

An observational study in Ovarian Cancer, sponsored by M.D. Anderson Cancer Center. Completed at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-08-01.

Sponsored by M.D. Anderson Cancer Center · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
237
Ages
18 Years and older
Sex
Female
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Study summary

The objective of this study is to evaluate the willingness of patients with ovarian cancer to undergo genetic testing, given the cost, their understanding and acceptance of genetic testing and the possibility of targeted therapy.

Read the detailed description

All eligible patients being seen in the Gynecology Center at the M.D. Anderson Cancer Center and at Gynecologic Oncology of Houston for follow-up or a new diagnosis of ovarian cancer will be asked to participate in this study by completing a questionnaire.

This study will end when 400 completed questionnaires have been collected. We estimate that 40-60 ovarian cancer patients are seen in the Gynecology Center at the M.D. Anderson Cancer Center each week and that 20- 40 ovarian cancer patients are seen at Gynecologic Oncology of Houston each week. The completion of 400 questionnaires will provide adequate data to address our question in an expeditious time frame. The initial phase of this study is exploratory and does not involve a comparison group.

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Conditions studied

  • Ovarian Cancer

Keywords

  • Ovarian Cancer
  • Questionnaire
  • Genetic Testing
  • Survey
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In context

Ovarian Neoplasms

2,695 studies on the registry are indexed under Ovarian Neoplasms; 727 are open to participants now.

This study's enrollment of 237 is above the median of 200 across 527 observational studies indexed under Ovarian Neoplasms.

Browse Ovarian Neoplasms studies →

Lead sponsor

M.D. Anderson Cancer Center is the lead sponsor of 2,999 studies on the registry; 581 are open to participants now.

Of its 599 completed or terminated interventional studies of FDA-regulated products, 402 (67%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Study participants with a diagnosis of ovarian cancer.

Inclusion criteria

  • Patients must have the diagnosis of ovarian cancer.
  • Patients must be at least 18 years of age at the time of enrollment.
  • Patients must be able to read and write in the English language.

Exclusion criteria

Exclusion Criteria:

  • Patients that are unable to speak or write in the English language. Currently, the investigators' resources in genetic counseling are limited. In the future, they plan to expand the questionnaire and study to include additional languages.
  • Patients having previously undergone BRCA genetic testing.
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
237 participants (actual)

Groups and cohorts

  • Patients with ovarian cancer

    Behavioral: Questionnaire

Interventions

  • BehavioralQuestionnaire

    A questionnaire will be completed.

    Also known as: Survey

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What researchers measure

Primary outcomes

  1. Participants' Response to Survey Questions (Yes/No)

    Time frame: 15-20 minutes to complete survey

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Study locations

1 site
  • U.T.M.D. Anderson Cancer Center
    Houston, Texas 77030, United States
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References and documents

Publications

  • Lacour RA, Daniels MS, Westin SN, Meyer LA, Burke CC, Burns KA, Kurian S, Webb NF, Pustilnik TB, Lu KH. What women with ovarian cancer think and know about genetic testing. Gynecol Oncol. 2008 Oct;111(1):132-6. doi: 10.1016/j.ygyno.2008.06.016. Epub 2008 Aug 6. PubMed 18684498 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00486707
Lead sponsor
M.D. Anderson Cancer Center
Responsible party
Sponsor
First posted
Jun 15, 2007
Start date
Jun 2007
Primary completion
Oct 2008
Completion
Oct 2008
Last update
Aug 1, 2012

Study contacts

Karen H. Lu, MD
principal investigator · M.D. Anderson Cancer Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.

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