Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
43 participants
OBSERVATIONAL
2024-04-05
2027-10-31
Brief Summary
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Detailed Description
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Determine the impact of educational videos on:
* Participant's hereditary cancer knowledge.
* Participant's confidence to share hereditary cancer information with family members.
Secondary Objective
* Determine impact of educational videos on participant's confidence to undergo hereditary cancer screening.
* Identify opportunities to tailor and improve the educational video's content, style, and understandability per participant preferences and feedback.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Interview Study
In the interview study, participants will watch the video, then complete an interview. This will take about 50 minutes.
Interview Study
All study participants will have the following demographic information collected from their medical records:
* Sex (Male/Female/Other)
* Date of birth
* Preferred language (English/Spanish)
* Health insurance status (for example: private insurance, HCHD "gold card")
* Cancer diagnosis (if yes: cancer type/organ, date of pathology diagnosis)
* Genetic testing result (gene with pathogenic/likely pathogenic variant)
* Date of genetic testing result
* Date of documented result disclosure.
Survey Study
In the survey study, participants will complete a survey about your education and complete a quick test about your knowledge of hereditary cancer. Participants will then watch the video. complete another survey similar to the one before the video. This should take about 30 minutes.
Survey Study
All study participants will have the following demographic information collected from their medical records:
* Sex (Male/Female/Other)
* Date of birth
* Preferred language (English/Spanish)
* Health insurance status (for example: private insurance, HCHD "gold card")
* Cancer diagnosis (if yes: cancer type/organ, date of pathology diagnosis)
* Genetic testing result (gene with pathogenic/likely pathogenic variant)
* Date of genetic testing result
* Date of documented result disclosure.
Interventions
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Interview Study
All study participants will have the following demographic information collected from their medical records:
* Sex (Male/Female/Other)
* Date of birth
* Preferred language (English/Spanish)
* Health insurance status (for example: private insurance, HCHD "gold card")
* Cancer diagnosis (if yes: cancer type/organ, date of pathology diagnosis)
* Genetic testing result (gene with pathogenic/likely pathogenic variant)
* Date of genetic testing result
* Date of documented result disclosure.
Survey Study
All study participants will have the following demographic information collected from their medical records:
* Sex (Male/Female/Other)
* Date of birth
* Preferred language (English/Spanish)
* Health insurance status (for example: private insurance, HCHD "gold card")
* Cancer diagnosis (if yes: cancer type/organ, date of pathology diagnosis)
* Genetic testing result (gene with pathogenic/likely pathogenic variant)
* Date of genetic testing result
* Date of documented result disclosure.
Eligibility Criteria
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Inclusion Criteria
2. 18 years of age or older.
3. Speaks and/or reads English or Spanish.
4. Has a pathogenic or likely pathogenic variant (mutation) in BRCA1, BRCA2, MLH1, MSH2, MSH6, PMS2, and/or EPCAM on germline genetic testing.
5. Has a documented genetic testing results disclosure encounter (i.e. telephone call, follow-up appointment).
Exclusion Criteria
2. Has only a variant of uncertain significance in BRCA1, BRCA2, MLH1, MSH2, MSH6, PMS2, and/or EPCAM.
3. Has only a pathogenic or likely pathogenic variant in gene other than BRCA1, BRCA2, MLH1, MSH2, MSH6, PMS2, or EPCAM.
4. Is unwilling, unable, or requires a legally authorized representative to provide informed consent.
18 Years
ALL
No
Sponsors
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M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Jose Rauh-Hain, MD
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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MD Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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MD Anderson Cancer Center
Other Identifiers
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NCI-2023-10074
Identifier Type: OTHER
Identifier Source: secondary_id
2023-0654
Identifier Type: -
Identifier Source: org_study_id
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