Trials / Completed
CompletedNCT04257045
Factors Influencing Cascade Testing Among Women With Hereditary Gynecological Cancers and Their Relatives
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 46 (actual)
- Sponsor
- M.D. Anderson Cancer Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
This trial collects information about factors that affect communication of genetic test results, decision-making, and access to genetic testing in women with hereditary gynecological cancers. Studying individuals who are positive for a genetic mutation and immediate biological family members (including a parent, full-sibling, or child) may help identify cancer genes and other persons at risk.
Detailed description
PRIMARY OBJECTIVES: I. Identify and explore factors influencing the communication of genetic testing results from probands (patients with confirmed hereditary cancer predisposition syndrome) to their first-degree relatives. (Step 1) II. Identify and explore factors influencing decision making and pursuit of cascade testing among first-degree relatives of probands. (Step 1) III. Estimate the uptake of cascade testing by first-degree relatives of probands at a safety-net hospital and the uptake of cascade testing by first-degree relatives of probands at a comprehensive cancer center. (Step 2) IV. Estimate the frequency of reported factors that influence communication, decision-making, and pursuit of cascade testing among probands and their first-degree family members at a safety-net hospital and at a comprehensive cancer center. (Step 2) V. Explore similarities and differences in cascade genetic testing rates and reported barriers to cascade genetic testing of first-degree relatives at probands from a safety-net hospital and a comprehensive cancer center. (Step 2) OUTLINE: STEP I: Patients and first degree relatives participate in semi-structure, in-depth interviews about genetic testing over 45-60 minutes. STEP II: Patients and first degree relatives complete survey questionnaires over 20 minutes.
Conditions
- Breast Carcinoma
- Deleterious CDH1 Gene Mutation
- Deleterious DICER1 Gene Mutation
- Deleterious SMARCA4 Gene Mutation
- Deleterious STK11 Gene Mutation
- Endometrial Carcinoma
- Fallopian Tube Carcinoma
- Ovarian Carcinoma
- Primary Peritoneal Carcinoma
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Interview | Participate in semi-structure, in-depth qualitative interviews |
| OTHER | Questionnaire Administration | Complete questionnaires |
| OTHER | Survey Administration | Complete survey |
Timeline
- Start date
- 2019-08-21
- Primary completion
- 2024-07-09
- Completion
- 2024-07-09
- First posted
- 2020-02-05
- Last updated
- 2024-07-12
Locations
2 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT04257045. Inclusion in this directory is not an endorsement.