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A Social Media Approach to Improve Genetic Risk Communication Phase I

23 de maio de 2019 atualizado por: M.D. Anderson Cancer Center
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.

Visão geral do estudo

Descrição detalhada

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.

Tipo de estudo

Observacional

Inscrição (Antecipado)

49

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Texas
      • Houston, Texas, Estados Unidos, 77030
        • University of Texas MD Anderson Cancer Center

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Método de amostragem

Amostra Não Probabilística

População do estudo

Participants recruited from Lynch syndrome families enrolled in the Human Pedigree Analysis Resource (HPAR), MDACC's hereditary cancer registry.

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Modelos de observação: Familiar
  • Perspectivas de Tempo: Prospectivo

Coortes e Intervenções

Grupo / Coorte
Intervenção / Tratamento
Group 1
Patients participate in audiotaped focus group regarding web-based program, and fill out demographics questionnaire.
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.
Complete questions about demographics (age, race, marital status) and medical history. This visit should take about 1 hour to complete.
Outros nomes:
  • Pesquisas
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.
Complete questions about demographics (age, race, marital status) and medical history. This visit should take about 1 hour to complete.
Outros nomes:
  • Pesquisas

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.

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.
Complete questions about demographics (age, race, marital status) and medical history. This visit should take about 1 hour to complete.
Outros nomes:
  • Pesquisas

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.

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

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Evaluation of Internet-Based Program Among Lynch Syndrome Family Members
Prazo: 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.
1 day

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Colaboradores

Investigadores

  • Investigador principal: Susan Peterson, MPH, PhD, M.D. Anderson Cancer Center

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de fevereiro de 2013

Conclusão Primária (Antecipado)

1 de fevereiro de 2020

Conclusão do estudo (Antecipado)

1 de fevereiro de 2021

Datas de inscrição no estudo

Enviado pela primeira vez

18 de julho de 2012

Enviado pela primeira vez que atendeu aos critérios de CQ

19 de julho de 2012

Primeira postagem (Estimativa)

20 de julho de 2012

Atualizações de registro de estudo

Última Atualização Postada (Real)

28 de maio de 2019

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de maio de 2019

Última verificação

1 de maio de 2019

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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