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Genetic Information Assistant in Telegenetics

Primary Purpose

Gene Mutation-Related Cancer, Genetic Predisposition

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Genetic Information Assistant
Telegenetics with UVA genetic counselor
Sponsored by
University of Virginia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Gene Mutation-Related Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: At high risk for having a genetic pathogenic variant as assessed by a GC or physician according to the NCCN guidelines Provision of signed and dated informed consent form. Stated willingness to comply with all study procedures and availability for the duration of the study. Male or female, aged 18 and over. Subjects must have a smartphone with access to cellular and/or internet service or a computer with internet service. Subjects must have technological competency/proficiency to use their Smartphone and/or computer in conjunction with the communication aid GIA. Exclusion Criteria: Cannot communicate in English or Spanish. Subjects must not have completed panel-based cancer genetic testing in the past.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Standard of care telegenetics with a UVA genetic counselor (GC) for pre-test counseling

    Novel interventional arm of pre-test counseling via GIA

    Arm Description

    Pre-genetic test counselling with a genetic counselor from the University of Virginia

    Pre-genetic test counselling through novel chat bot Genetic Information Assistant (GIA)

    Outcomes

    Primary Outcome Measures

    To assess feasibility of using a chatbot (GIA) for pre-test genetic counseling compared to standard of care GC
    dichotomous measurement of whether the randomized participant completes genetic testing within three months.

    Secondary Outcome Measures

    To test cancer knowledge following the pre-test genetic counseling with GIA versus GC
    National Center for Human Genome Research Knowledge scale taken at baseline and one month after genetic testing.
    To assess differences of Comprehensive Score of Financial Toxicity scale
    To assess the difference in comprehensive score between one- and six-months of Comprehensive Score for Financial Toxicity (COST) survey. Scoring: 0 (Poor Financial well-being) to 48 (Better financial well-being)
    To assess differences of SURE scale
    To assess the difference in comprehensive scores of the following surveys between one- and six-months of SURE scale. Scoring 0-4: Score <4 is a positive result for decisional conflict.
    To assess differences of Decisional Conflict scale
    To assess the difference in comprehensive scores of the following surveys between one- and six-months Decisional Conflict Scale. Scoring: 0 (no decisional conflict) to 100 (extremely high decisional conflict)
    To assess differences of Multi-dimensional Impact of Cancer Risk Assessment (MICRA) scale
    To assess the difference in comprehensive scores of the following surveys between one- and six-months Multi-dimensional Impact of Cancer Risk Assessment (MICRA) survey

    Full Information

    First Posted
    October 11, 2023
    Last Updated
    October 17, 2023
    Sponsor
    University of Virginia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06089421
    Brief Title
    Genetic Information Assistant in Telegenetics
    Official Title
    A Prospective, Randomized Trial to Compare Telegenetics to Counseling Via a Novel Genetic Information Assistant in High-risk Cancer Patients.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 20, 2023 (Anticipated)
    Primary Completion Date
    March 15, 2025 (Anticipated)
    Study Completion Date
    March 15, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Virginia

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The goal of this clinical trial is to learn about different ways cancer genetic screening can be provided to rural communities in participants at high risk for certain cancers. The main question it aims to answer is: • Does receiving pre-genetic test education with a chat bot or genetic counselor affect if the participant decides to get genetic testing? Participants will: have a pre-test genetic counselling session with a genetic counselor or the GIA chatbot answer questions about their cancer genetic knowledge and how they are doing provide a saliva sample for genetic testing to test for cancer gene mutations have their genetic testing results provided to them. have the option to share their genetic testing results with family members Researchers will compare how many participants who had pre-genetic counseling with the chatbot received genetic testing to how many participants who had pre-genetic counseling with a genetic counselor received genetic testing.
    Detailed Description
    High risk patients will be randomized to standard of care telegenetics with a UVA Genetic Counselor (GC) for pre-test counseling or to the novel interventional arm of pre-test counseling via Genetic Information Assistant (GIA). Participants in the study will receive their link for a telegenetics appointment or GIA link based on randomization and patients will complete pre-test genetic counseling via their assigned treatment arm. Participants will not be masked to their trial arm assignment. In the telegenetics arm, patients will be offered a video visit scheduled through Epic zoom or a phone visit in our cancer genetics clinic per standard of care. Patients randomized to the GIA arm will receive a personalized link based on their family history. At the completion of counseling, participants will be offered genetic testing. If they agree, they will be mailed a saliva kit via Invitae Genetics for panel based genetic testing via The Invitae Common Hereditary Cancers panel to analyze 47 genes associated with cancers of the breast, ovary, uterus, and gastrointestinal system, which includes the stomach, colon, rectum, small bowel, and pancreas.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Gene Mutation-Related Cancer, Genetic Predisposition

    7. Study Design

    Primary Purpose
    Screening
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    96 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Standard of care telegenetics with a UVA genetic counselor (GC) for pre-test counseling
    Arm Type
    Active Comparator
    Arm Description
    Pre-genetic test counselling with a genetic counselor from the University of Virginia
    Arm Title
    Novel interventional arm of pre-test counseling via GIA
    Arm Type
    Experimental
    Arm Description
    Pre-genetic test counselling through novel chat bot Genetic Information Assistant (GIA)
    Intervention Type
    Other
    Intervention Name(s)
    Genetic Information Assistant
    Intervention Description
    Participants assigned will receive a link to Genetic Information Assistant for pre-test counseling.
    Intervention Type
    Other
    Intervention Name(s)
    Telegenetics with UVA genetic counselor
    Intervention Description
    Participants assigned will have a pre-test counseling session via a telegentics visit with a genetic counselor.
    Primary Outcome Measure Information:
    Title
    To assess feasibility of using a chatbot (GIA) for pre-test genetic counseling compared to standard of care GC
    Description
    dichotomous measurement of whether the randomized participant completes genetic testing within three months.
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    To test cancer knowledge following the pre-test genetic counseling with GIA versus GC
    Description
    National Center for Human Genome Research Knowledge scale taken at baseline and one month after genetic testing.
    Time Frame
    3 months
    Title
    To assess differences of Comprehensive Score of Financial Toxicity scale
    Description
    To assess the difference in comprehensive score between one- and six-months of Comprehensive Score for Financial Toxicity (COST) survey. Scoring: 0 (Poor Financial well-being) to 48 (Better financial well-being)
    Time Frame
    6 months
    Title
    To assess differences of SURE scale
    Description
    To assess the difference in comprehensive scores of the following surveys between one- and six-months of SURE scale. Scoring 0-4: Score <4 is a positive result for decisional conflict.
    Time Frame
    6 months
    Title
    To assess differences of Decisional Conflict scale
    Description
    To assess the difference in comprehensive scores of the following surveys between one- and six-months Decisional Conflict Scale. Scoring: 0 (no decisional conflict) to 100 (extremely high decisional conflict)
    Time Frame
    6 months
    Title
    To assess differences of Multi-dimensional Impact of Cancer Risk Assessment (MICRA) scale
    Description
    To assess the difference in comprehensive scores of the following surveys between one- and six-months Multi-dimensional Impact of Cancer Risk Assessment (MICRA) survey
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: At high risk for having a genetic pathogenic variant as assessed by a GC or physician according to the NCCN guidelines Provision of signed and dated informed consent form. Stated willingness to comply with all study procedures and availability for the duration of the study. Male or female, aged 18 and over. Subjects must have a smartphone with access to cellular and/or internet service or a computer with internet service. Subjects must have technological competency/proficiency to use their Smartphone and/or computer in conjunction with the communication aid GIA. Exclusion Criteria: Cannot communicate in English or Spanish. Subjects must not have completed panel-based cancer genetic testing in the past.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Graham Fowler
    Phone
    (434) 323-1749
    Email
    NVG4WM@uvahealth.org
    First Name & Middle Initial & Last Name or Official Title & Degree
    Magnifique Irakoze
    Phone
    (434) 924-9918
    Email
    rve7xg@virginia.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Kari Ring, MD
    Organizational Affiliation
    University of Virginia
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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