A Social Media Approach to Improve Genetic Risk Communication Phase I

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT01645904
Collaborator
Duncan Family Institute (Other)
49
1
96
0.5

Study Details

Study Description

Brief Summary

The goal of this research study is to create an internet-based program designed to improve the communication of health and health history information among family members affected by Lynch syndrome.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Audiotaped Focus Group
  • Behavioral: Demographic Questionnaire
  • Behavioral: Audiotaped Interview
  • Behavioral: WAMMI Inventory

Detailed Description

If you agree to take part in this study, you will be assigned to 1 of 3 groups based on when you joined the study.

Group 1:

If you are assigned to Group 1, you will take part in a focus group where you will be asked what you would want in a web-based program designed to improve the communication of health and health history information among family members affected by Lynch syndrome. You will also fill out a questionnaire with questions about your demographics (age, race, marital status) and your medical history. This visit should take about 1 hour to complete.

Group 2:

If you are assigned to Group 2, you will come to the Behavioral Research and Treatment Center (BRTC) at MD Anderson to use the initial version of the My Family Garden website. My Family Garden is designed to teach new ways of communicating about Lynch Syndrome and about other issues related to the disease (such as risks associated with the disease, etc.). You will be instructed on how to use the program by the study staff. After you use the website, you will have an interview where you will provide feedback on your session. You will be asked questions about your feelings about the website and about any possible improvements that could be made to the website. You will also fill out a questionnaire called the Website Analysis and MeasureMent Inventory (WAMMI) which is designed help rate websites. You will also fill out the demographics questionnaire described above.

You will be given the option of completing the WAMMI and demographics questionnaire at the BRTC after your session or at your home. If you choose to complete them at home, you will be provided with a self-addressed, postage-paid envelope so you can mail the questionnaires back to the study staff.

This visit should take about 90 minutes to complete.

Group 3:

If you are assigned to Group 3, you will use the final version of the My Family Garden website. This final version will include changes from the web designers after feedback has been given from the previous groups in this study.

After you use the website, you will have an interview where you will provide feedback on your session. You will be asked questions about your feelings about the website and about any possible improvements that could be made to the website. You will also fill out the WAMMI questionnaire and demographics questionnaire described above.

You will be given the option of coming to the BRTC at MD Anderson to use the My Family Garden computer program or using the program from your home. If you choose to use My Family Garden from your home, you will be given a secure, password-protected hyperlink via e-mail to access the program. You will be instructed on how to use the program by the study staff either in person or over the phone. If you use the program from your home, the study staff will give the interview over the phone. If you complete the questionnaire at your home, you will be provided with a self-addressed, postage-paid envelope so you can mail it back to the study staff.

Whether it is completed at MD Anderson or at home, this visit should last about 90 minutes.

Audiotapes:

All focus groups and interviews will be audiotaped. The audiotapes collected during the course of this study will be stored in locked file cabinets in a locked office and will be destroyed after 5 years.

Length of Study Participation:

Your participation in this study will be over after you have completed the study procedures described above.

This is an investigational study.

Up to 49 participants will be enrolled in this study. All participants will be enrolled at MD Anderson.

Study Design

Study Type:
Observational
Anticipated Enrollment :
49 participants
Observational Model:
Family-Based
Time Perspective:
Prospective
Official Title:
A Social Media Approach to Improve Genetic Risk Communication Phase I
Actual Study Start Date :
Feb 1, 2013
Anticipated Primary Completion Date :
Feb 1, 2020
Anticipated Study Completion Date :
Feb 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Group 1

Patients participate in audiotaped focus group regarding web-based program, and fill out demographics questionnaire.

Behavioral: Audiotaped Focus Group
Participation in a focus group regarding web-based program designed to improve communication of health and health history information among family members affected by Lynch syndrome.

Behavioral: Demographic Questionnaire
Complete questions about demographics (age, race, marital status) and medical history. This visit should take about 1 hour to complete.
Other Names:
  • Surveys
  • Group 2

    Patients come to Behavioral Research and Treatment Center (BRTC) at MD Anderson to use initial version of My Family Garden website. Completion of Website Analysis and MeasureMent Inventory (WAMMI), and demographics questionnaires.

    Behavioral: Demographic Questionnaire
    Complete questions about demographics (age, race, marital status) and medical history. This visit should take about 1 hour to complete.
    Other Names:
  • Surveys
  • Behavioral: Audiotaped Interview
    Group 2: Patients provide feedback regarding initial version of My Family Garden website. Group 3: Patients provide feedback regarding final version of My Family Garden website.

    Behavioral: WAMMI Inventory
    Patients complete Website Analysis and MeasureMent Inventory. This visit should take about 90 minutes to complete.

    Group 3

    Patients use final version of My Family Garden website, and are interviewed which will be audiotaped. Completion of Website Analysis and MeasureMent Inventory (WAMMI), questionnaire and demographics questionnaire.

    Behavioral: Demographic Questionnaire
    Complete questions about demographics (age, race, marital status) and medical history. This visit should take about 1 hour to complete.
    Other Names:
  • Surveys
  • Behavioral: Audiotaped Interview
    Group 2: Patients provide feedback regarding initial version of My Family Garden website. Group 3: Patients provide feedback regarding final version of My Family Garden website.

    Behavioral: WAMMI Inventory
    Patients complete Website Analysis and MeasureMent Inventory. This visit should take about 90 minutes to complete.

    Outcome Measures

    Primary Outcome Measures

    1. Evaluation of Internet-Based Program Among Lynch Syndrome Family Members [1 day]

      Quantitative analysis include descriptive statistics summarizing participants' demographic and clinical characteristics. Descriptive statistics calculated for each subscale of Website Analysis and MeasureMent Inventory (WAMMI) and for overall measure. Focus groups and interviews transcribed, coded and analyzed. Responses sorted into categorical and conceptual groups, field notes taken during user testing also used to aid in interpretation of interview data.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. At least 18 years of age

    2. Able to read and speak english

    3. Completion of genetic counseling and testing for a Lynch syndrome mutation

    4. Persons with positive (i.e., carrier of Lynch syndrome MMR mutation) as well as indeterminate test results

    Exclusion Criteria:
    1. None

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Texas MD Anderson Cancer Center Houston Texas United States 77030

    Sponsors and Collaborators

    • M.D. Anderson Cancer Center
    • Duncan Family Institute

    Investigators

    • Principal Investigator: Susan Peterson, MPH, PhD, M.D. Anderson Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT01645904
    Other Study ID Numbers:
    • 2012-0418
    First Posted:
    Jul 20, 2012
    Last Update Posted:
    May 28, 2019
    Last Verified:
    May 1, 2019

    Study Results

    No Results Posted as of May 28, 2019