Evaluation of Hereditary Cancer Educational Videos

NCT ID: NCT06157801

Last Updated: 2025-09-08

Study Results

Results pending

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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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

43 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-04-05

Study Completion Date

2027-10-31

Brief Summary

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To learn if educational videos can help participants be more informed about hereditary cancers (ones that run in the family).

Detailed Description

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Primary Objective

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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Hereditary Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

Intervention Type BEHAVIORAL

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

Intervention Type BEHAVIORAL

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.

Intervention Type BEHAVIORAL

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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Participants of The Harris Health System Lyndon B. Johnson (LBJ) Hospital outpatient oncology clinics (i.e., Gynecologic Oncology, Medical Oncology).
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

1. No longer receives outpatient care at LBJ Hospital at time of recruitment.
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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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United States

Related Links

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http://www.mdanderson.org

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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